Oral tolerance in the absence of naturally occurring Tregs
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《临床调查学报》
1Program of Molecular Pathogenesis, Skirball Institute of Biomolecular Medicine, New York University School of Medicine, New York, New York, USA.
2Departmento de Imunologia, Universidade de So Paulo, So Paulo, Brazil.
3Department of Pathology, New York University School of Medicine, New York, New York, USA.
Abstract
Mucosal tolerance prevents pathological reactions against environmental and food antigens, and its failure results in exacerbated inflammation typical of allergies and asthma. One of the proposed mechanisms of oral tolerance is the induction of Tregs. Using a mouse model of hyper-IgE and asthma, we found that oral tolerance could be effectively induced in the absence of naturally occurring thymus-derived Tregs. Oral antigen administration prior to i.p. immunization prevented effector/memory Th2 cell development, germinal center formation, class switching to IgE, and lung inflammation. Oral exposure to antigen induced development of antigen-specific CD4+CD25+Foxp3+CD45RBlow cells that were anergic and displayed suppressive activity in vivo and in vitro. Oral tolerance to the Th2 allergic response was in large part dependent on TGF- and independent of IL-10. Interestingly, Tregs were also induced by single i.p. immunization with antigen and adjuvant. However, unlike oral administration of antigen, which induced Tregs but not effector T cells, i.p. immunization led to the simultaneous induction of Tregs and effector Th2 cells displaying the same antigen specificity.
Introduction
Oral tolerance can be defined as an inhibition of specific immune responsiveness to subsequent parenteral injections of proteins to which an individual or animal has been previously exposed via the oral route (1-4). Several mechanisms have been proposed for the development of oral tolerance, ranging from the deletion of antigen-specific T cells (5, 6) to immune deviation (7, 8), induction of anergy (9), and suppression by Tregs (10, 11).
When markers of naturally occurring Tregs, such as CD45RBlow, CD25, cytotoxic T lymphocyte–associated antigen 4 (CTLA-4), glucocorticoid-induced TNF receptor (GITR), and, more recently, the forkhead box transcription factor Foxp3 became available, a number of studies described a role for naturally occurring Tregs in the development of oral or inhaled tolerance (10-17). However, these studies did not address the issue of whether naturally occurring Tregs are necessary for the induction of oral tolerance.
The possible role of Tregs as mediators of oral tolerance has been addressed by directly feeding antigen to TCR-transgenic mice (10, 11, 18) and by using TCR transgenic mice as a source of naive antigen–specific T cells in transfer systems (11, 14, 15). In all these experimental systems, the influence of thymic-derived naturally occurring Tregs could not be ruled out, either because the studies were carried out in TCR transgenic recombination activating gene (RAG+) systems or because antigen-specific T cells were transferred to wild-type mice, which have a full complement of naturally occurring Tregs. The influence of these host-derived Tregs on the behavior of the antigen-specific TCR transgenic T cells could not be assessed. It has been shown that TCR transgenic RAG+ mice harbor antigen-specific Tregs, but virtually all of these Tregs coexpress 1 or 2 TCR chains encoded by endogenous TCR genes. It is believed that endogenous TCR chains are essential for the thymic differentiation of antigen-specific TCR transgenic Tregs, which are absent in most TCR transgenic RAG–/– mice (19).
It has become increasingly apparent in the past several months that cells indistinguishable from naturally occurring thymic-derived CD4+CD25+Foxp3+ Tregs can be generated in vivo in the periphery of experimental animals. The peripheral conversion of naive CD4+CD25– T cells from TCR-transgenic RAG–/– mice into functional antigen-specific CD4+CD25+Foxp3+ Tregs was shown by Apostolou and von Boehmer, after s.c. infusion of the TCR transgene-specific peptide ligand (20), and by Cobbold et al., after sex-mismatched skin grafting performed together with coreceptor blockade (21). We have shown that about 10–15% of naive CD4+CD25–Foxp3– T cells convert into functional CD4+CD25+Foxp3+ Tregs upon homeostatic proliferation (22). In addition to these examples of Tregs that are very similar to thymic-derived naturally occurring Tregs, it has been known for some time that regulatory cells displaying a range of differences from naturally occurring Tregs could be generated in vivo in peripheral tissues. For instance, CD8+ DCs isolated from mice immunized with heat-killed Listeria monocytogenes induced Tregs that display some Th1 properties (23). Immunization with certain GAD65 peptides led to the development of cells that resemble Tr1 Tregs (24). Administration of myelin basic protein peptides i.n. also resulted in the generation of IL-10–producing Tregs (25), which are Foxp3 negative (26). Epicutaneous immunization was shown to induce CD4+CD25– Tregs (27). Importantly, oral administration led to the generation of TGF-–producing Treg (Th3) cells (28). Finally, in vitro approaches have demonstrated that naive T cells activated in the presence of TGF- generate CD4+CD25+Foxp3+ Tregs that resemble naturally occurring Tregs (29-31).
Using an experimental asthma model, we here show that mice devoid of naturally occurring Tregs are highly susceptible to the induction of oral tolerance after being fed antigen in drinking water. Oral antigen administration impairs the development of effector/memory Th2 cells and germinal centers (GC), class switching to IgE, and lung inflammation. Moreover, oral exposure to antigen leads to the generation of peripheral antigen-specific CD4+CD25+CD45RBlow Tregs that express Foxp3 and CTLA-4. Our results demonstrate that oral tolerance induction does not require naturally occurring thymus-derived Tregs, as functional Tregs of similar characteristics are induced by oral antigen administration.
Results
OVA feeding suppresses asthma-like responses in the absence of naturally occurring thymus-derived Tregs.
We sought to determine whether oral tolerance to an allergic response could be induced in the absence of thymus-derived Tregs. To address this issue, we used a strain of mice hereafter referred to as T/B monoclonal mice, generated by the cross of (a) influenza HA–specific immunoglobulin heavy- and light-chain knockin mice (32); (b) DO11.10 OVA-specific T cell receptor transgenic mice (33); and (c) RAG-1 knockout mice (34), and (d) extensively backcrossed onto BALB/c background. The T/B monoclonal mice provide an excellent model system to study the requirement for thymic-derived Tregs during oral tolerance, since these mice carry naive populations of T and B lymphocytes, are devoid of Tregs, and develop exacerbated Th2/IgE responses and lung inflammation after i.p. immunization and respiratory challenge with the cognate antigen OVA-HA (32). The protocol to induce and test oral tolerance and the various experimental groups is indicated in Figure 1A. In brief, T/B monoclonal mice were administered OVA in drinking water for 5 days and immunized i.p. 2 days later with OVA-HA in alum. To elicit an asthma-like inflammatory response, mice were administered OVA-HA i.n. on days 14 and 21 after i.p. immunization (35, 36). Analysis of lung inflammation was performed 1 day after the second respiratory challenge.
The quantity and composition of the cellular exudate in the airways were determined through the harvesting and analysis of cells in the bronchoalveolar lavage (BAL). Inflammation in the lung parenchyma and goblet cell activation was determined by H&E and PAS staining of lung sections. Figure 1, B and C, shows the analysis of airway inflammation in immunized mice that did or did not receive OVA in drinking water. Those that received OVA in the drinking water prior to OVA-HA i.p. immunization and i.n. administration were referred to as the tolerant group (Tol), and those that received only the latter 2 treatments were referred to as the immune group (Imm) (Figure 1A). Immunization and respiratory challenge of T/B monoclonal mice with OVA-HA elicited intense infiltration of eosinophils, neutrophils, and lymphocytes in the airways, cellular inflammation of the lung parenchyma, and production of mucus by goblet cells (Figure 1, B and C; Imm group). In contrast, mice pretreated with OVA in the drinking water displayed much-reduced airway inflammation (Figure 1, B and C; Tol group). In particular, eosinophil numbers in BAL were reduced by more than 10-fold. Oral antigen administration also prevented goblet cell activation and inflammation of lung parenchyma (Figure 1C; compare the stained sections from Imm and Tol mice).
Oral administration of OVA suppresses hyper-IgE and -IgG1 responses.
Tol group mice displayed a robust inhibition of both hyper-IgE and -IgG1 antibody production, as demonstrated by the reduced levels of these 2 isotypes in serum (Figure 2A) and BAL (Figure 2B) compared with those in the Imm group. IgA, although described as an isotype induced by oral tolerance (2), was also lower in tolerant mice. Since the B cells in the T/B monoclonal mice do not recognize OVA and the HA peptide was not included in the oral treatment, it is understandable that IgA antibodies were not induced during OVA feeding. Production of IgG2a antibodies did not differ between the Tol and Imm groups. IgG2a antibody levels after i.p. immunization were about 100-fold lower than IgG1 levels, as the response of the T/B monoclonal mice is dominated by Th2-dependent isotypes (32). Analysis of spleen and mesenteric lymph node (mLN) cells on days 10 and 22 after i.p. immunization demonstrated that the oral administration of OVA prevented Th2 differentiation (measured by IL-4 production; Supplemental Figure 1; supplemental material available online with this article; doi:10.1172/JCI24487DS1), formation of GCs (Supplemental Figure 1, B and C), and immunoglobulin class switching (Supplemental Figure 1B). Altogether, these results demonstrate that oral tolerance to a Th2 response can be efficiently induced in the absence of naturally occurring Tregs.
In the experiments described above, oral antigen administration preceded i.p. immunization. In order to determine whether this sequence of treatments was necessary for effective induction of tolerance, we performed experiments in which oral OVA administration was started on the same day as i.p. OVA-HA immunization. No tolerance was observed with this protocol, as demonstrated by analysis of lung inflammation, BAL cellular content, and IgE production (Supplemental Figure 2).
Oral OVA administration affects the activation of OVA-specific T lymphocytes after i.p. immunization.
Immunization of T/B monoclonal mice with i.p. OVA-HA leads to the activation and differentiation of OVA-specific T cells (22, 32). The early phase of the T cell response lasts about 4 days and is characterized by the swift upregulation of CD25 and CD69 expression and IL-2 secretion, followed by proliferation and, finally, contraction of the T cell population. The late phase takes place mostly during the second week after immunization and is characterized by the appearance of effector Th cells (CD45RBlowCD44hi) that secrete IL-4 (22, 32). Since we showed that IL-4 production was inhibited in the animals exposed to OVA in the drinking water, we sought to determine whether the early phase of the T cell response was also affected. Toward that end, we analyzed the kinetics of CD25 and CD69 expression in spleen cells of mice after i.p. immunization. We found that CD25 and CD69 upregulation was similar in the Imm and Tol groups at 24 hours after i.p. immunization (Figure 3A; top panels). However, cells of Tol group mice expressed lower levels of CD69 and CD25 at 48 hours (Figure 3A; middle panels). Although at 48 hours, overall CD25 levels were lower in the Tol group mice, a population of CD25hiCD45RBlow T cells (the phenotype of Tregs) was increased in this group (Figure 3B). By 96 hours, CD69 and CD25 were downregulated in both the Imm and Tol groups (Figure 3A; bottom panels). These results indicate that previous administration of OVA in the drinking water curtails the early T cell–activation phase induced by subsequent i.p. immunization with OVA-HA.
CD45RB is expressed at high levels on naive T cells and is downregulated in antigen-experienced cells (37). The CD45RBhiCD25+ population represents recently activated cells, whereas the CD45RBlow is a heterogeneous population containing differentiated effector/memory T cells (contained in the CD45RBlowCD25– population) and Treg cells (the CD45RBlowCD25+ population) (38-40). To determine how oral tolerance affects the differentiation of T cells into cells with effector/memory phenotype and Tregs, we quantified CD45RBlowCD25– and CD45RBlowCD25+ in mLN, spleen, and BAL cells of the Oral (mice fed OVA in drinking water; see Figure 1A), Imm, and Tol groups at several time points after immunization. Figure 4A shows FACS plots of CD25 and CD45RB expression in gated CD4+KJ1-26+ cells from the mLNs of animals pre-exposed or not pre-exposed to OVA in the drinking water, 22 days after i.p. immunization. The Tol and Imm groups displayed comparable frequencies of CD25+CD45RBlow T cells, but the Imm group reproducibly had a higher percentage of effector/memory T cells (Figure 4A). The same stainings and quadrants shown in Figure 4A were utilized for the kinetic studies shown in Figure 4B. Analysis of mLNs at day 0 (prior to i.p. immunization) showed that OVA-fed animals (Oral group and Tol group) already had an increased proportion of both CD25–CD45RBlow and CD25+CD45RBlow T cells, reflecting prior exposure to antigen. At later time points, the proportion of CD25+CD45RBlow T cells increased in the Tol group, which received i.p. immunization, unlike the Oral group. The increase in the proportion of CD25–CD45RBlow populations over time was most marked in the Imm group whereas the increase in the proportion of CD25+CD45RBlow cells was more or less parallel in the Tol and Imm groups (Figure 4B). Similar results were obtained with spleen samples (Supplemental Figure 3, A and B). When we analyzed the BAL cells after respiratory challenge, we found that the Tol group had more CD25+CD45RBlow cells than CD25–CD45RBlow cells while the converse was true for the mice of the Imm group (Figure 4C).
The above results show that CD25+CD45RBlow cells, which have the surface phenotype of Tregs, develop in all mice exposed to oral OVA, i.p. OVA-HA, or both. By the time of i.p. immunization, CD25+CD45RBlow cells were already present in mice that had received oral OVA, and their numbers further increased with immunization. The population of CD25–CD45RBlow cells also developed in all mouse groups exposed to OVA, but it became proportionally larger only in mice of the Imm group, in which the first antigen exposure was by the i.p. route. Thus, oral immunization, compared with i.p. immunization, favors the induction of CD25+CD45RBlow cells over the induction of CD25–CD45RBlow cells.
Oral tolerance induces Foxp3+CD25+ Tregs.
To determine whether the CD25+CD45RBlow cells induced in the T/B monoclonal mice exposed to oral OVA and/or i.p. OVA-HA were bona fide Tregs, we studied the expression of Treg-associated genes Foxp3 and CTLA-4 in purified CD4+CD25+ and CD4+CD25– cells. Unlike other Treg markers, Foxp3 expression has been reported as not being upregulated in conventional mouse T cells upon their activation (41-43). Thus, Foxp3 expression is the marker that best correlates with Treg function. We also analyzed the expression of cytokines associated with suppressor (IL-10, TGF-) or effector (IL-4, IL-5, and IFN-) activity.
CD4+CD25– and CD4+CD25+ cells were purified by magnetic sorting from pooled spleen and mLN cells at several time points after i.p. immunization, and mRNA expression in the samples was determined by quantitative real-time PCR. Two days after i.p. immunization, Foxp3 expression by the CD4+CD25+ T cells in the Tol group was approximately 100 times higher than in the Imm group (Figure 5A). On day 4, the levels of Foxp3 expression in CD4+CD25+ T cells from Tol mice were 5–6 times higher than in those from the Imm group. Foxp3 expression was also detected in CD4+CD25+ T cells from mice that received OVA orally but were not immunized i.p. (Figure 5A; Oral group: days 0, 4, 10, and 22). In the 3 experimental groups, Foxp3 levels in the CD4+CD25+ samples were similar on days 10 and 22. Foxp3 expression was virtually undetected in CD4+CD25– T cells from any group at any time point. CTLA-4 expression in the CD25+ population paralleled Foxp3 expression (Supplemental Figure 4A). High IL-4 and IL-5 production were only detected in the CD25– population of the Imm group (Figure 5B and Supplemental Figure 4F). The expression of IL-10 and IFN- was relatively low in all groups (Supplemental Figure 4, B and C). We did not detect consistent differences in the levels of expression of TGF- or SMAD2 by purified populations of CD4+CD25– or CD4+CD25+ cells from any group (Supplemental Figure 4, D and E).
In sum, Foxp3 expression was observed in the CD4+CD25+ T cells from all experimental groups exposed to OVA, either orally, i.p., or both. The main difference found among the groups was in the high expression of the Th2 cytokines IL-4 and IL-5 in the Imm group; expression of these cytokines was undetectable in mice that had previously received oral OVA (Oral and Tol groups). Thus, oral administration of antigen induces OVA-specific naive T cell differentiation to Tregs but not to Th2 effector cells. In contrast, i.p. immunization induces both Th2 and Tregs. In this case, the fact that Tregs develop at the same time as Th2 cells and not before may explain the inability of the Tregs to suppress Th2 differentiation and the asthmatic response.
Tregs generated in T/B monoclonal mice suppress in vitro proliferation and in vivo IgE responses.
We next assessed the suppressor activity of oral tolerance–induced antigen-specific CD4+CD25+ T cells using a standard in vitro assay. CD4+CD25+ and CD4+CD25– T cells were purified from spleen and mLN cells from Tol group mice on day 10 after i.p. immunization. These cells were tested for their ability to proliferate upon anti-CD3 antibody stimulation and to suppress the proliferation of purified CD4+CD25– cells from wild-type BALB/c mice. As shown in Figure 6, CD4+CD25+ T cells from Tol-group mice were as anergic and suppressive as freshly isolated CD4+CD25+ T cells from wild-type BALB/c mice whereas CD4+CD25– T cells from Tol-group mice exhibited high proliferation in response to anti-CD3 stimulation and no suppressor activity.
We also tested to determine whether the transfer of OVA-specific CD4+CD25+ cells from Tol-group mice could suppress in vivo the IgE response to OVA-HA. CD4+CD25+ and CD4+CD25– T cells were purified from Tol-group mice on day 10 after i.p. immunization. These purified cells were transferred into BALB/c mice with or without naive anti-OVA T cells and/or naive anti-HA B cells, and recipient mice were immunized 1 day after. On day 14 after immunization, the production of IgG1 and IgE as well as the expansion of OVA-specific T cells were determined. The 2 experiments indicated in Figure 7, A and B, showed that OVA-specific CD4+CD25+ cells from Tol-group mice diminished IgE production and overall expansion of OVA-specific T cells (identified by staining with the anti-clonotypic antibody KJ1-26). In contrast, OVA-specific CD25– cells from the Tol group did not suppress naive cell responses; furthermore, these cells were able to proliferate and provide help for IgE production at levels comparable to those seen in naive OVA-specific T cells (Figure 7B). These results confirm that OVA-specific Tregs generated in T/B monoclonal mice after oral exposure and immunization are suppressive in vivo and in vitro. Moreover, the results show that IgE responses can be attained (and regulated) in a transfer system into BALB/c mice in a way that is qualitatively similar to T/B monoclonal mice, although displaying lower overall IgE values.
We also investigated whether cells with Treg phenotypes induced after i.p. immunization could suppress the Th2/IgE response. We purified CD25+ cells from T/B monoclonal mice that had either been immunized i.p. with OVA-HA (Imm group) or had received OVA orally and subsequently been immunized i.p. with OVA-HA (Tol group). In both groups cell purification was performed 10 days after i.p. immunization. A total of 5 x 105 CD4+CD25+ T cells were transferred to naive T/B monoclonal mice, and the mice were immunized i.p. 1 day later with OVA-HA in alum. As shown in Figure 7C, cells from both the Imm- and the Tol-group mice efficiently suppressed the IgE response. Thus, both oral administration of antigen and i.p. immunization with adjuvant induce functional Tregs, but in the latter case, Treg development does not occur sufficiently early to affect the course of the concomitant Th2 response.
IL-10 is not necessary for the induction of oral tolerance in T/B monoclonal mice.
The mechanism of suppression by naturally occurring Tregs in vitro is cell-contact dependent and cytokine independent whereas the cytokines IL-10 and TGF- have been shown to be important for in vivo suppression in several experimental models (44-46). In addition, both IL-10 and TGF- were found to have the ability to induce Treg activity in vitro. While TGF- has been implicated in oral tolerance, the role of IL-10 in oral tolerance is controversial (4, 47, 48). We next investigated to determine whether IL-10 and TGF- are required for induction of oral tolerance in the absence of thymus-derived Tregs.
IL-10–deficient T/B monoclonal mice were generated by crossing T/B monoclonal mice with BALB/c IL-10–/– mice. As shown in Figure 8, IL-10–/– T/B monoclonal mice developed hyper–IgE response and airway inflammation after i.p. immunization and respiratory challenge. However, when compared to that in IL-10+ T/B monoclonal mice (Figures 1 and 2), serum IgE and eosinophilia in IL-10–/– T/B monoclonal mice were modestly but reproducibly reduced. Oral OVA administration before i.p. immunization resulted in suppression of all asthma parameters analyzed, namely BAL eosinophilic infiltrate, lung inflammation, and mucus secretion (Figure 8, A and C). Interestingly, neutrophilic infiltration was not reduced in Tol group IL-10–/– T/B monoclonal mice, probably because lung neutrophilic infiltration is mediated by Th1 cells (49-51). From the early days of IL-10 research, it has been known that IL-12 and IFN-, 2 critical cytokines in Th1 biology, are targets of IL-10 inhibition (52). Thus, it is not surprising that this particular aspect of lung inflammation is not significantly reduced in Tol group T/B monoclonal IL-10–deficient mice.
IL-10–/– T/B monoclonal mice of the Tol group displayed strong inhibition of B cell responses, such as the production of IgG1 and IgE (Figure 8B) and GC reaction (Supplemental Figure 5A). Like tolerance induction in IL-10+ T/B monoclonal mice, that in IL-10–/– mice was accompanied by a lower accumulation of CD45RBlowCD25– (effector/memory T cells) cells (Supplemental Figure 5B). IL-10–/– T/B monoclonal mice were also susceptible to nasal tolerance (Supplemental Figure 6). Thus, in this experimental system, IL-10 is not necessary either for the development of the asthmatic response or for the establishment of effective mucosal tolerance.
TGF- is required for oral tolerance in T/B monoclonal mice.
We tested next to determine whether TGF- was required during the initial oral tolerization phase. To this end, we injected T/B monoclonal mice with the depleting anti–TGF- antibody 1D11 before, during, and immediately after oral OVA administration. As shown in Figure 9, neutralization of TGF- impaired oral tolerization, reverting suppression of eosinophilic airway inflammation, production of IL-4 by cells in BAL, and production of seric IgG1 and IgE (Figure 9, A–C). We also observed a reversion of the suppression of GC formation (Supplemental Figure 7A) and of the development of CD45RBlowCD25– T cells (Supplemental Figure 7B).
To determine the role of TGF- in the in vivo differentiation of Tregs during OVA feeding, we administered anti–TGF- antibody 1 day before and 2 days after the beginning of oral treatment. On day 5 of oral treatment (Figure 1A; day –2), we analyzed the expression of CD25 and CD45RB in mLN cells. We observed an increase in CD45RBlowCD25+ cells (as well as in recently activated CD45RBhiCD25+ cells) in mice that received OVA orally compared with untreated T/B monoclonal mice (Figure 10A). The same analysis enabled us to confirm that, as expected, unimmunized T/B monoclonal mice have no CD45RBlowCD25+ cells, the region in the FACS plot in which Tregs are found (Figure 10A). Anti–TGF- treatment resulted in only a moderate reduction of the CD45RBlowCD25+ population (Figure 10A). In order to determine Foxp3 expression levels, we FACS-sorted the 4 populations defined by anti-CD45RB and anti-CD25 antibodies from mLNs and prepared cDNA for real-time PCR analysis. As anticipated, only CD45RBlowCD25+ cells expressed Foxp3. Importantly, anti–TGF- treatment resulted in a 2- to 3-fold reduction of Foxp3 expression in mLN cells (Figure 10B). The reduction in Foxp3 expression was even more marked in spleen cells (Supplemental Figure 8).
Figure 10
Neutralization of TGF- in vivo inhibits early Foxp3 expression. T/B monoclonal mice were injected with anti–TGF- 1 day before and 3 days after the beginning of administration of 1% OVA in the drinking water. After 5 days of oral-OVA, CD4+ mLN cells were analyzed for expression of CD45RB and CD25 by FACS and for expression of Foxp3 by real-time PCR. (A) mLN cells from mice that received oral-OVA alone, from mice that received anti–TGF- antibodies and oral-OVA, and from untreated T/B monoclonal mice were stained with antibodies for CD4, CD45RB, and CD25. The figure shows representative plots of CD4+ gated cells. (B) CD4+ cells from pooled mLN (4 mice per group) were sorted in a MoFlo flow cytometer into CD45RBlowCD4+CD25+, CD45RBlowCD4+CD25–, CD45RBhiCD4+CD25+, and CD45RBhiCD4+CD25– fractions. Foxp3 expression in the samples was determined by real-time PCR. Results are expressed as mean ± SD of triplicate wells.
Our results are consistent with the notion that oral antigen administration induces antigen-specific Tregs in a process that requires TGF- for full Foxp3 induction. Our results from the adoptive transfer experiments strongly support the notion that antigen-specific Tregs induced by oral tolerance prevent asthma-type responses by inhibiting Th2 differentiation and class switching to IgE in the lymphoid organs.
Discussion
In this manuscript, we make 2 main observations. The first is that oral tolerance can be induced in the absence of thymic-derived Tregs. Establishment of oral tolerance correlates with the de novo induction of antigen-specific CD4+CD25+Foxp3+ Tregs, which is impaired when TGF- is blocked. Second, we show that a single immunization with antigen plus adjuvant leads to the generation of functional antigen-specific Tregs, which, in this case, occurs in parallel with the generation of effector Th2 cells.
Several mechanisms have been proposed to account for oral tolerance, such as clonal deletion of antigen-specific T cells, immune deviation, T cell anergy, and the induction of Tregs (4, 47, 53). In fact, the transfer of tolerance by Tregs obtained from animals that have been fed antigen has been known for more than 25 years (54, 55). It has been shown, using OVA-specific DO11.10 TCR transgenic mice, that in tolerant mice there is an increase in the CD4+CD25+ population. These CD25+ cells prevented a delayed type hypersensitivity response upon transfer into BALB/c mice (56). Several groups have used adoptive transfer of DO11.10 OVA-TCR transgenic T cells into wild-type animals to demonstrate the induction of CD4+ cells that are able to transfer tolerance (11, 14, 57). Recently, Ostroukhova et al. (17) described Foxp3 expression in antigen-stimulated cultures of membrane TGF-+CD4+ T cells from mice tolerized to OVA by respiratory antigen exposure. Stock et al. showed that splenic CD8+ DC from mice tolerized to OVA through the airways induced antigen-specific Tregs that expressed Foxp3, Tbet, IFN-, and IL-10 (23). In these and other studies, a direct or inductive role for thymus-derived Tregs in antigen-specific tolerance could not be ruled out.
To clarify in a definitive manner the need for thymus-derived Treg cells in oral tolerance, we studied mucosal tolerance in mice that lack naturally occurring thymus-derived Tregs (Figure 10A) and showed that oral administration of OVA previous to i.p. immunization with OVA-HA dramatically suppressed an asthmatic inflammatory response in these mice.
We also observed that tolerance was associated with the induction of antigen-specific CD4+CD25+ cells that expressed markers of naturally occurring Tregs, such as Foxp3 and CTLA-4 (13, 41-43). CD4+CD25+ cells induced by oral antigen administration behaved as naturally occurring Tregs, as they were anergic and suppressive upon stimulation with anti-CD3 antibodies in vitro. Importantly, transfer of these cells led to suppression of the IgE response. Thus, oral delivery of antigen induced antigen-specific naive CD4 cells to become Tregs by a process that is independent of the presence of thymic-derived Tregs. Although we did not formally exclude the possibility that orally administered OVA makes its way to the thymus and promotes the development of immature cells into Tregs, we believe that this possibility is unlikely given the relatively rapid appearance of CD25+Foxp3+ cells (Figure 10, A and B) and recent reports demonstrating antigen-induced generation of Tregs in thymectomized animals (20) and the conversion of naive mature peripheral CD25–Foxp3– T cells into Tregs in a transfer system (22).
The generation of antigen-specific Tregs by oral administration of antigen explains the discrepancies between our conclusions and those of Dubois and coworkers (16). These authors concluded that naturally occurring Tregs are required for oral tolerance. They antibody-depleted CD25+ cells in B6 mice and showed that oral tolerance was abrogated. However, since the last antibody treatment was performed 7 days after the oral feeding, it is likely that the authors depleted not only the naturally occurring Tregs but also those Tregs that had been peripherally generated by the oral feeding.
Recently, Apostolou and von Boehmer showed that continuous subcutaneous antigen delivery induced Foxp3+ Tregs that were indistinguishable from naturally occurring Tregs (20). Our results extend those of Apostolou and von Boehmer by demonstrating that antigen-specific Tregs can be induced by mucosal delivery of antigen. Importantly, we found that a single parenteral immunization in the presence of antigen also induced Treg development. In this case, however, Tregs were induced concomitantly to Th2 cells.
If antigen-specific Tregs can be generated upon single immunization even in the presence of adjuvant, one may wonder why these Treg do not control the primary immune response. In fact, as we previously reported, T/B monoclonal mice develop hyper-Th2 and hyper-IgE responses after a single immunization, indicating lack of regulation. The explanation is provided by our kinetic data (Figures 4, 5, and 10), which show that high Foxp3 expression is attained only 10 days after a single i.p. immunization of T/B monoclonal mice. At this time, there is already a robust Th2 response. In order to inhibit Th2 differentiation and hyper-IgE production, regulation has to be in place before day 4 after immunization (Supplemental Figure 9), which is not the case during the normal course of the response in T/B monoclonal mice. However, while the Tregs generated by parenteral exposure to antigen in T/B monoclonal mice are not able to control the primary immune response, they may help downregulate further responses or reduce the damage caused by chronic antigenic stimulation. Accordingly, we observed that in T/B monoclonal mice repeatedly immunized i.p. with OVA-HA, there was an increase in Foxp3 levels and a decrease in IL-4 production by CD25– T cells (Supplemental Figure 10).
The role of IL-10 in mucosal tolerance is controversial (13, 17, 18, 58, 59). In the model of hyper-IgE and asthma described here, oral tolerance did not require IL-10, since IL-10–/– T/B monoclonal mice were as susceptible to oral tolerance as their IL-10+ littermates. However, neutrophilic inflammation was not ameliorated by oral tolerance in IL-10–/– mice.
The key role of TGF- in oral tolerance was established long ago (60, 61). In contrast, experiments with TGF-1–/– mice showed that oral tolerance could be achieved in the absence of TGF-1, although the degree of inhibition of the response by antigen feeding was much lower in TGF-1–/– mice than in TGF-1+ control mice (62). This experimental system was further complicated by anti–lymphocyte function-associated antigen-1–antibody (anti–LFA-1–antibody) treatment of the mice. In our experimental model, blockade of TGF- caused an almost complete reversal of the suppression of GC formation and memory T cell development while other parameters, such as eosinophilia and IgE production, were only partially, albeit significantly, reversed. At this time we do not know whether the residual suppression of IgE and eosinophilia was due to incomplete neutralization of TGF- or to the fact that a small fraction of the suppression operates via TGF-–independent mechanisms. For instance, the suppression of neutrophil numbers in BAL was not reversed by anti–TGF- antibodies, which is consistent with the fact the suppression of neutrophil migration may be dependent on IL-10.
It is not completely clear whether, in vivo, TGF- is an inductive stimulus for Treg generation, an effector molecule that mediates Treg suppressive function, or both. It has been proposed that oral administration of antigens induces Th3 cells. The TGF- produced by Th3 cells would be a major effector molecule in the suppression of responses (28). However, the role of TGF- in the induction of Th3 cells in the mucosa has not been determined. Our results show that blockade of TGF- in vivo abolishes oral tolerance and considerably impairs the induction of CD25+Foxp3+ Tregs. Given the lack of markers that uniquely identify Th3 cells, the relationship between the Foxp3+ cells that we describe here and Th3 cells has not been determined. However, oral tolerance in our model was not accompanied by enhanced concentration of active TGF- in the airways (data not shown), suggesting that, in this model, TGF- acts as an inductor of Tregs but not as an effector molecule in the suppression of asthma-like symptoms.
It has been shown that in vitro treatment of cells with TGF- induces regulatory cells that are more (21, 29, 31, 63) or less (64) similar to naturally occurring Tregs. Thus, our results confirm previous observations on the importance of TGF- in oral tolerance and extend those observations to include the differentiation of antigen-specific Foxp3+CD4+ Tregs in vivo upon oral administration of antigen.
The importance of TGF- in the generation of CD25+Foxp3+ Tregs in the periphery contrasts with the fact that naturally occurring Tregs can be generated in the absence of TGF-1 (65). Thus, although peripherally generated and thymic-derived naturally occurring Tregs have essentially the same phenotype and functional characteristics, they differ in the TGF- requirement for their generation. TGF- appears to have a role in the homeostasis of both naturally occurring and peripherally generated CD4+CD25+Foxp3+ Tregs (66-68). It is likely that a similar situation occurs for IL-2. IL-2 is not needed for the thymic generation of naturally occurring Tregs (22, 69, 70) but is required for the peripheral maintenance and function of naturally occurring Tregs and probably for the peripheral induction of Tregs (22, 69). It is evident now that Foxp3+CD25+ Tregs can be of thymic or peripheral origin and that additional factors are needed for the peripheral generation of Tregs that are not necessary for the generation of naturally occurring thymic-derived Tregs.
The fact that conventional immunization protocols lead to the generation of Tregs is of significance. Since, before i.p. immunization, naive OVA-specific T cells that will become Tregs cannot be distinguished from those that will become Th2 cells, it remains to be determined whether generation of Tregs versus that of effector T cells is a stochastic process or some microenvironmental conditions promote the development of one cell type over the other. The fact that mucosal administration of antigen promotes the development of Tregs with very little Th2 differentiation favors the second possibility.
Methods
Mice.
The T/B monoclonal mice (17/9 DO11.10 RAG1–/–) bearing monoclonal populations of T and B lymphocytes specific for chicken ovalbumin 323–339 and HA of influenza virus, respectively, were generated as previously described (32). BALB/c mice were purchased from Taconic or the Jackson Laboratory. BALB/c IL-10–/– mice were obtained from Donna Rennick (DNAX, Palo Alto, California, USA). TCR–/––/–, DO11.10 TCR–/––/–, and 17/9 DO11.10 RAG1–/– IL-10–/– mice (T/B monoclonal IL10–/– mice) were all backcrossed into a BALB/c genetic background for more than 10 generations. All IL-10–/– mice were kept on sulfamethoxazole (400 mg/l) and trimethoprim (80 mg/l) in their drinking water, except for the days in which they received OVA orally. All mice were bred and housed under specific pathogen-free conditions at the Skirball Institute animal facility. All procedures involving animals were approved by the New York University School of Medicine Institutional Animal Care and Use Committee.
Oral antigen administration, immunization, and airway challenge.
Oral tolerance to OVA was induced by offering to the animals, ad libitum, a 1% OVA (grade II; Sigma-Aldrich) solution dissolved in drinking water for 5 consecutive days. The HA peptide (YPYDVPDYASLRS) was synthesized by ResGen. Crosslinked OVA-HA was prepared as previously described (32). Immunization with OVA-HA was performed i.p. with 100 μg of OVA-HA adsorbed to 1 mg of alum, 2 days after the end of the oral treatment. To induce airway inflammation, anesthetized mice were administered 10 μg of OVA-HA i.n. in 50 μl of PBS (25 μl in each nostril) on days 14 and 21 after i.p. immunization. For TGF- neutralization, mice were injected i.p. with 2 mg of the anti–TGF- monoclonal antibody 1D11 on 1 day before and 2, 5, and 8 days after the beginning of oral treatment.
BAL collection and lung histology.
Mice were deeply anesthetized by i.p. injection of anesthetic solution containing ketamine and xylazine. The tracheae were cannulated, and lungs were lavaged twice, once with 0.5 ml and once with 1.0 ml PBS. After total cell counting, cytospin preparations of the BAL cells were stained with DiffQuik (Baxter Dade AG), and differential cell counts were performed on 200 cells on the basis of morphology and staining characteristics. Student’s t test was used for statistical analysis.
Lungs were removed after BAL collection, perfused via the right ventricle with 10-ml saline to remove residual blood, fixed with phosphate-buffered formalin, and embedded in paraffin. Tissue sections were stained with H&E to determine cellular inflammation or with PAS/hematoxylin for evaluation of mucus-producing cells.
Serum and BAL antibodies.
Total and HA-specific antibodies in serum or BAL samples were quantified by ELISA as described (32). Purified and biotinylated antibodies to Ig isotypes and standard purified immunoglobulin isotypes were purchased from BD Biosciences — Pharmingen and CALTAG Laboratories. Serum titer was defined as the lowest dilution that rendered an OD value higher than 0.1 after background subtraction.
FACS analysis.
Single cell suspensions in staining buffer (PBS containing 2% fetal calf serum and 0.1% NaN3) were incubated for 45 minutes at 4°C with the antibody cocktails. Samples were analyzed in a FACSCalibur instrument (BD). FITC-labeled and biotin-labeled HA peptides were purchased from ResGen. Peanut agglutinin–FITC and peanut agglutinin–biotin were purchased from Vector Laboratories. The remaining antibodies were purchased from BD Biosciences — Pharmingen and CALTAG Laboratories.
Cytokine production ex vivo.
Cytokine production was analyzed ex vivo by intracellular staining. Briefly, cells were stimulated with 1-μM OVA 323–339 peptide for 4 hours. During the last 2 hours, cells were incubated with monensin (Sigma-Aldrich) to inhibit secretion. Cells were then surface stained with FITC-labeled KJ1–26 and PerCP-labeled anti-CD4 antibodies, fixed, permeabilized, stained with PE-labeled anti–IL-4 antibodies, and analyzed in a FACSCalibur.
Cell purification and transfer.
CD4+CD25+ and CD4+CD25– lymphocytes were purified from spleen and mLN cells by magnetic sorting using Miltenyi Biotec reagents and VarioMACS apparatus as described (22). Cell purity was checked by FACS analysis. The CD25+ purified fraction contained no more than 3% CD4+CD25– contamination. Purified CD25– cells contained 0.5–2% of CD25low cells and no CD25high cells. 3–5 x 105 purified cells were injected i.v. into recipient mice. In some experiments, CD4+CD25+ and CD4+CD25– cells were sorted in a MoFlo apparatus at the NYU Sorting Facility.
RNA analysis.
For quantitative mRNA expression analysis, CD4+CD25– and CD25+ cells were purified using either magnetic sorting or MoFlo sorting as described (22). RNA was extracted from samples using TRIzol (Invitrogen Corp.), and cDNA was synthesized by standard procedures. The expression of Foxp3, CTLA-4, IL-4, IFN-, and -actin was determined by quantitative real-time PCR. Primers for Foxp3, CTLA-4, and -actin were as described (22). Other primer sequences are as follows: IL-4: ACAGGAGAAGGGACGCCATG and GCAGCTTATCGATGAATCCA; IFN-: GCTTTGCAGCTCTTCCTCAT and TCTTCCACATCTATGCCACTTG; TGF-: CTGCTGACCCCCACTGATA and GCTGAATCGAAAGCCCTGTA; SMAD2: CCGGCTGAACTGTCTCCTAC and ATAGTATGCGATTGAACACCAGAATG; IL-10: TCCCCTGTGAAAATAAGAGCA and TGGCCTTGTAGACACCTTGG; and IL-5: AGCAATGAGACGATGAGGC and ACACTTCTCTTTTTGGCGGT.
In vitro suppression assay.
CD4+CD25– and CD25+ cells from T/B monoclonal mice as well as fresh BALB/c CD4+CD25– and CD25+ cells were purified using magnetic sorting. Proliferation assays were set up in 96-well round bottom plates and contained, per well, the following: 2 x 104 responder cells (CD4+CD25– BALB/c cells); 4 x 104 APCs (mitomycin C–treated spleen cells from TCR-deficient BALB/c mice); and anti-CD3 antibody at a concentration of 0.5 mg/ml. Putative suppressor cells were cocultured at responder/suppressor ratios of 1.0:1.0, 1.0:0.3, and 1.0:0.1. Proliferation was determined by adding 3H-thymidine on the third day of culture and determining incorporation 6 hours later.
Acknowledgments
Work in the J.J. Lafaille laboratory is supported by the NIH/National Institute of Allergy and Infectious Diseases, the National Multiple Sclerosis Society, and the Dana-Goldsmith Foundation. D. Mucida was a recipient of a predoctoral fellowship from Coordenaao de Aperfeioamento de Pessoal de Nivel Superior, Brazil. D. Mucida would like to thank Ana M.C. de Faria, Nelson M. Vaz, and A.C. Keller for very helpful discussions and suggestions.
Footnotes
Nonstandard abbreviations used: BAL, bronchoalveolar lavage; CTLA-4, cytotoxic T lymphocyte–associated antigen 4; GITR, glucocorticoid-induced TNF receptor; GC, germinal center; Imm, mice given OVA-HA i.p. immunization; mLN, mesenteric lymph node; Oral, mice fed OVA in drinking water; RAG, recombination activating gene; Th3 cell, TGF-–producing Treg cell; Tol, mice fed OVA in drinking water prior to OVA-HA i.p. immunization.
Conflict of interest: The authors have declared that no conflict of interest exists.
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2Departmento de Imunologia, Universidade de So Paulo, So Paulo, Brazil.
3Department of Pathology, New York University School of Medicine, New York, New York, USA.
Abstract
Mucosal tolerance prevents pathological reactions against environmental and food antigens, and its failure results in exacerbated inflammation typical of allergies and asthma. One of the proposed mechanisms of oral tolerance is the induction of Tregs. Using a mouse model of hyper-IgE and asthma, we found that oral tolerance could be effectively induced in the absence of naturally occurring thymus-derived Tregs. Oral antigen administration prior to i.p. immunization prevented effector/memory Th2 cell development, germinal center formation, class switching to IgE, and lung inflammation. Oral exposure to antigen induced development of antigen-specific CD4+CD25+Foxp3+CD45RBlow cells that were anergic and displayed suppressive activity in vivo and in vitro. Oral tolerance to the Th2 allergic response was in large part dependent on TGF- and independent of IL-10. Interestingly, Tregs were also induced by single i.p. immunization with antigen and adjuvant. However, unlike oral administration of antigen, which induced Tregs but not effector T cells, i.p. immunization led to the simultaneous induction of Tregs and effector Th2 cells displaying the same antigen specificity.
Introduction
Oral tolerance can be defined as an inhibition of specific immune responsiveness to subsequent parenteral injections of proteins to which an individual or animal has been previously exposed via the oral route (1-4). Several mechanisms have been proposed for the development of oral tolerance, ranging from the deletion of antigen-specific T cells (5, 6) to immune deviation (7, 8), induction of anergy (9), and suppression by Tregs (10, 11).
When markers of naturally occurring Tregs, such as CD45RBlow, CD25, cytotoxic T lymphocyte–associated antigen 4 (CTLA-4), glucocorticoid-induced TNF receptor (GITR), and, more recently, the forkhead box transcription factor Foxp3 became available, a number of studies described a role for naturally occurring Tregs in the development of oral or inhaled tolerance (10-17). However, these studies did not address the issue of whether naturally occurring Tregs are necessary for the induction of oral tolerance.
The possible role of Tregs as mediators of oral tolerance has been addressed by directly feeding antigen to TCR-transgenic mice (10, 11, 18) and by using TCR transgenic mice as a source of naive antigen–specific T cells in transfer systems (11, 14, 15). In all these experimental systems, the influence of thymic-derived naturally occurring Tregs could not be ruled out, either because the studies were carried out in TCR transgenic recombination activating gene (RAG+) systems or because antigen-specific T cells were transferred to wild-type mice, which have a full complement of naturally occurring Tregs. The influence of these host-derived Tregs on the behavior of the antigen-specific TCR transgenic T cells could not be assessed. It has been shown that TCR transgenic RAG+ mice harbor antigen-specific Tregs, but virtually all of these Tregs coexpress 1 or 2 TCR chains encoded by endogenous TCR genes. It is believed that endogenous TCR chains are essential for the thymic differentiation of antigen-specific TCR transgenic Tregs, which are absent in most TCR transgenic RAG–/– mice (19).
It has become increasingly apparent in the past several months that cells indistinguishable from naturally occurring thymic-derived CD4+CD25+Foxp3+ Tregs can be generated in vivo in the periphery of experimental animals. The peripheral conversion of naive CD4+CD25– T cells from TCR-transgenic RAG–/– mice into functional antigen-specific CD4+CD25+Foxp3+ Tregs was shown by Apostolou and von Boehmer, after s.c. infusion of the TCR transgene-specific peptide ligand (20), and by Cobbold et al., after sex-mismatched skin grafting performed together with coreceptor blockade (21). We have shown that about 10–15% of naive CD4+CD25–Foxp3– T cells convert into functional CD4+CD25+Foxp3+ Tregs upon homeostatic proliferation (22). In addition to these examples of Tregs that are very similar to thymic-derived naturally occurring Tregs, it has been known for some time that regulatory cells displaying a range of differences from naturally occurring Tregs could be generated in vivo in peripheral tissues. For instance, CD8+ DCs isolated from mice immunized with heat-killed Listeria monocytogenes induced Tregs that display some Th1 properties (23). Immunization with certain GAD65 peptides led to the development of cells that resemble Tr1 Tregs (24). Administration of myelin basic protein peptides i.n. also resulted in the generation of IL-10–producing Tregs (25), which are Foxp3 negative (26). Epicutaneous immunization was shown to induce CD4+CD25– Tregs (27). Importantly, oral administration led to the generation of TGF-–producing Treg (Th3) cells (28). Finally, in vitro approaches have demonstrated that naive T cells activated in the presence of TGF- generate CD4+CD25+Foxp3+ Tregs that resemble naturally occurring Tregs (29-31).
Using an experimental asthma model, we here show that mice devoid of naturally occurring Tregs are highly susceptible to the induction of oral tolerance after being fed antigen in drinking water. Oral antigen administration impairs the development of effector/memory Th2 cells and germinal centers (GC), class switching to IgE, and lung inflammation. Moreover, oral exposure to antigen leads to the generation of peripheral antigen-specific CD4+CD25+CD45RBlow Tregs that express Foxp3 and CTLA-4. Our results demonstrate that oral tolerance induction does not require naturally occurring thymus-derived Tregs, as functional Tregs of similar characteristics are induced by oral antigen administration.
Results
OVA feeding suppresses asthma-like responses in the absence of naturally occurring thymus-derived Tregs.
We sought to determine whether oral tolerance to an allergic response could be induced in the absence of thymus-derived Tregs. To address this issue, we used a strain of mice hereafter referred to as T/B monoclonal mice, generated by the cross of (a) influenza HA–specific immunoglobulin heavy- and light-chain knockin mice (32); (b) DO11.10 OVA-specific T cell receptor transgenic mice (33); and (c) RAG-1 knockout mice (34), and (d) extensively backcrossed onto BALB/c background. The T/B monoclonal mice provide an excellent model system to study the requirement for thymic-derived Tregs during oral tolerance, since these mice carry naive populations of T and B lymphocytes, are devoid of Tregs, and develop exacerbated Th2/IgE responses and lung inflammation after i.p. immunization and respiratory challenge with the cognate antigen OVA-HA (32). The protocol to induce and test oral tolerance and the various experimental groups is indicated in Figure 1A. In brief, T/B monoclonal mice were administered OVA in drinking water for 5 days and immunized i.p. 2 days later with OVA-HA in alum. To elicit an asthma-like inflammatory response, mice were administered OVA-HA i.n. on days 14 and 21 after i.p. immunization (35, 36). Analysis of lung inflammation was performed 1 day after the second respiratory challenge.
The quantity and composition of the cellular exudate in the airways were determined through the harvesting and analysis of cells in the bronchoalveolar lavage (BAL). Inflammation in the lung parenchyma and goblet cell activation was determined by H&E and PAS staining of lung sections. Figure 1, B and C, shows the analysis of airway inflammation in immunized mice that did or did not receive OVA in drinking water. Those that received OVA in the drinking water prior to OVA-HA i.p. immunization and i.n. administration were referred to as the tolerant group (Tol), and those that received only the latter 2 treatments were referred to as the immune group (Imm) (Figure 1A). Immunization and respiratory challenge of T/B monoclonal mice with OVA-HA elicited intense infiltration of eosinophils, neutrophils, and lymphocytes in the airways, cellular inflammation of the lung parenchyma, and production of mucus by goblet cells (Figure 1, B and C; Imm group). In contrast, mice pretreated with OVA in the drinking water displayed much-reduced airway inflammation (Figure 1, B and C; Tol group). In particular, eosinophil numbers in BAL were reduced by more than 10-fold. Oral antigen administration also prevented goblet cell activation and inflammation of lung parenchyma (Figure 1C; compare the stained sections from Imm and Tol mice).
Oral administration of OVA suppresses hyper-IgE and -IgG1 responses.
Tol group mice displayed a robust inhibition of both hyper-IgE and -IgG1 antibody production, as demonstrated by the reduced levels of these 2 isotypes in serum (Figure 2A) and BAL (Figure 2B) compared with those in the Imm group. IgA, although described as an isotype induced by oral tolerance (2), was also lower in tolerant mice. Since the B cells in the T/B monoclonal mice do not recognize OVA and the HA peptide was not included in the oral treatment, it is understandable that IgA antibodies were not induced during OVA feeding. Production of IgG2a antibodies did not differ between the Tol and Imm groups. IgG2a antibody levels after i.p. immunization were about 100-fold lower than IgG1 levels, as the response of the T/B monoclonal mice is dominated by Th2-dependent isotypes (32). Analysis of spleen and mesenteric lymph node (mLN) cells on days 10 and 22 after i.p. immunization demonstrated that the oral administration of OVA prevented Th2 differentiation (measured by IL-4 production; Supplemental Figure 1; supplemental material available online with this article; doi:10.1172/JCI24487DS1), formation of GCs (Supplemental Figure 1, B and C), and immunoglobulin class switching (Supplemental Figure 1B). Altogether, these results demonstrate that oral tolerance to a Th2 response can be efficiently induced in the absence of naturally occurring Tregs.
In the experiments described above, oral antigen administration preceded i.p. immunization. In order to determine whether this sequence of treatments was necessary for effective induction of tolerance, we performed experiments in which oral OVA administration was started on the same day as i.p. OVA-HA immunization. No tolerance was observed with this protocol, as demonstrated by analysis of lung inflammation, BAL cellular content, and IgE production (Supplemental Figure 2).
Oral OVA administration affects the activation of OVA-specific T lymphocytes after i.p. immunization.
Immunization of T/B monoclonal mice with i.p. OVA-HA leads to the activation and differentiation of OVA-specific T cells (22, 32). The early phase of the T cell response lasts about 4 days and is characterized by the swift upregulation of CD25 and CD69 expression and IL-2 secretion, followed by proliferation and, finally, contraction of the T cell population. The late phase takes place mostly during the second week after immunization and is characterized by the appearance of effector Th cells (CD45RBlowCD44hi) that secrete IL-4 (22, 32). Since we showed that IL-4 production was inhibited in the animals exposed to OVA in the drinking water, we sought to determine whether the early phase of the T cell response was also affected. Toward that end, we analyzed the kinetics of CD25 and CD69 expression in spleen cells of mice after i.p. immunization. We found that CD25 and CD69 upregulation was similar in the Imm and Tol groups at 24 hours after i.p. immunization (Figure 3A; top panels). However, cells of Tol group mice expressed lower levels of CD69 and CD25 at 48 hours (Figure 3A; middle panels). Although at 48 hours, overall CD25 levels were lower in the Tol group mice, a population of CD25hiCD45RBlow T cells (the phenotype of Tregs) was increased in this group (Figure 3B). By 96 hours, CD69 and CD25 were downregulated in both the Imm and Tol groups (Figure 3A; bottom panels). These results indicate that previous administration of OVA in the drinking water curtails the early T cell–activation phase induced by subsequent i.p. immunization with OVA-HA.
CD45RB is expressed at high levels on naive T cells and is downregulated in antigen-experienced cells (37). The CD45RBhiCD25+ population represents recently activated cells, whereas the CD45RBlow is a heterogeneous population containing differentiated effector/memory T cells (contained in the CD45RBlowCD25– population) and Treg cells (the CD45RBlowCD25+ population) (38-40). To determine how oral tolerance affects the differentiation of T cells into cells with effector/memory phenotype and Tregs, we quantified CD45RBlowCD25– and CD45RBlowCD25+ in mLN, spleen, and BAL cells of the Oral (mice fed OVA in drinking water; see Figure 1A), Imm, and Tol groups at several time points after immunization. Figure 4A shows FACS plots of CD25 and CD45RB expression in gated CD4+KJ1-26+ cells from the mLNs of animals pre-exposed or not pre-exposed to OVA in the drinking water, 22 days after i.p. immunization. The Tol and Imm groups displayed comparable frequencies of CD25+CD45RBlow T cells, but the Imm group reproducibly had a higher percentage of effector/memory T cells (Figure 4A). The same stainings and quadrants shown in Figure 4A were utilized for the kinetic studies shown in Figure 4B. Analysis of mLNs at day 0 (prior to i.p. immunization) showed that OVA-fed animals (Oral group and Tol group) already had an increased proportion of both CD25–CD45RBlow and CD25+CD45RBlow T cells, reflecting prior exposure to antigen. At later time points, the proportion of CD25+CD45RBlow T cells increased in the Tol group, which received i.p. immunization, unlike the Oral group. The increase in the proportion of CD25–CD45RBlow populations over time was most marked in the Imm group whereas the increase in the proportion of CD25+CD45RBlow cells was more or less parallel in the Tol and Imm groups (Figure 4B). Similar results were obtained with spleen samples (Supplemental Figure 3, A and B). When we analyzed the BAL cells after respiratory challenge, we found that the Tol group had more CD25+CD45RBlow cells than CD25–CD45RBlow cells while the converse was true for the mice of the Imm group (Figure 4C).
The above results show that CD25+CD45RBlow cells, which have the surface phenotype of Tregs, develop in all mice exposed to oral OVA, i.p. OVA-HA, or both. By the time of i.p. immunization, CD25+CD45RBlow cells were already present in mice that had received oral OVA, and their numbers further increased with immunization. The population of CD25–CD45RBlow cells also developed in all mouse groups exposed to OVA, but it became proportionally larger only in mice of the Imm group, in which the first antigen exposure was by the i.p. route. Thus, oral immunization, compared with i.p. immunization, favors the induction of CD25+CD45RBlow cells over the induction of CD25–CD45RBlow cells.
Oral tolerance induces Foxp3+CD25+ Tregs.
To determine whether the CD25+CD45RBlow cells induced in the T/B monoclonal mice exposed to oral OVA and/or i.p. OVA-HA were bona fide Tregs, we studied the expression of Treg-associated genes Foxp3 and CTLA-4 in purified CD4+CD25+ and CD4+CD25– cells. Unlike other Treg markers, Foxp3 expression has been reported as not being upregulated in conventional mouse T cells upon their activation (41-43). Thus, Foxp3 expression is the marker that best correlates with Treg function. We also analyzed the expression of cytokines associated with suppressor (IL-10, TGF-) or effector (IL-4, IL-5, and IFN-) activity.
CD4+CD25– and CD4+CD25+ cells were purified by magnetic sorting from pooled spleen and mLN cells at several time points after i.p. immunization, and mRNA expression in the samples was determined by quantitative real-time PCR. Two days after i.p. immunization, Foxp3 expression by the CD4+CD25+ T cells in the Tol group was approximately 100 times higher than in the Imm group (Figure 5A). On day 4, the levels of Foxp3 expression in CD4+CD25+ T cells from Tol mice were 5–6 times higher than in those from the Imm group. Foxp3 expression was also detected in CD4+CD25+ T cells from mice that received OVA orally but were not immunized i.p. (Figure 5A; Oral group: days 0, 4, 10, and 22). In the 3 experimental groups, Foxp3 levels in the CD4+CD25+ samples were similar on days 10 and 22. Foxp3 expression was virtually undetected in CD4+CD25– T cells from any group at any time point. CTLA-4 expression in the CD25+ population paralleled Foxp3 expression (Supplemental Figure 4A). High IL-4 and IL-5 production were only detected in the CD25– population of the Imm group (Figure 5B and Supplemental Figure 4F). The expression of IL-10 and IFN- was relatively low in all groups (Supplemental Figure 4, B and C). We did not detect consistent differences in the levels of expression of TGF- or SMAD2 by purified populations of CD4+CD25– or CD4+CD25+ cells from any group (Supplemental Figure 4, D and E).
In sum, Foxp3 expression was observed in the CD4+CD25+ T cells from all experimental groups exposed to OVA, either orally, i.p., or both. The main difference found among the groups was in the high expression of the Th2 cytokines IL-4 and IL-5 in the Imm group; expression of these cytokines was undetectable in mice that had previously received oral OVA (Oral and Tol groups). Thus, oral administration of antigen induces OVA-specific naive T cell differentiation to Tregs but not to Th2 effector cells. In contrast, i.p. immunization induces both Th2 and Tregs. In this case, the fact that Tregs develop at the same time as Th2 cells and not before may explain the inability of the Tregs to suppress Th2 differentiation and the asthmatic response.
Tregs generated in T/B monoclonal mice suppress in vitro proliferation and in vivo IgE responses.
We next assessed the suppressor activity of oral tolerance–induced antigen-specific CD4+CD25+ T cells using a standard in vitro assay. CD4+CD25+ and CD4+CD25– T cells were purified from spleen and mLN cells from Tol group mice on day 10 after i.p. immunization. These cells were tested for their ability to proliferate upon anti-CD3 antibody stimulation and to suppress the proliferation of purified CD4+CD25– cells from wild-type BALB/c mice. As shown in Figure 6, CD4+CD25+ T cells from Tol-group mice were as anergic and suppressive as freshly isolated CD4+CD25+ T cells from wild-type BALB/c mice whereas CD4+CD25– T cells from Tol-group mice exhibited high proliferation in response to anti-CD3 stimulation and no suppressor activity.
We also tested to determine whether the transfer of OVA-specific CD4+CD25+ cells from Tol-group mice could suppress in vivo the IgE response to OVA-HA. CD4+CD25+ and CD4+CD25– T cells were purified from Tol-group mice on day 10 after i.p. immunization. These purified cells were transferred into BALB/c mice with or without naive anti-OVA T cells and/or naive anti-HA B cells, and recipient mice were immunized 1 day after. On day 14 after immunization, the production of IgG1 and IgE as well as the expansion of OVA-specific T cells were determined. The 2 experiments indicated in Figure 7, A and B, showed that OVA-specific CD4+CD25+ cells from Tol-group mice diminished IgE production and overall expansion of OVA-specific T cells (identified by staining with the anti-clonotypic antibody KJ1-26). In contrast, OVA-specific CD25– cells from the Tol group did not suppress naive cell responses; furthermore, these cells were able to proliferate and provide help for IgE production at levels comparable to those seen in naive OVA-specific T cells (Figure 7B). These results confirm that OVA-specific Tregs generated in T/B monoclonal mice after oral exposure and immunization are suppressive in vivo and in vitro. Moreover, the results show that IgE responses can be attained (and regulated) in a transfer system into BALB/c mice in a way that is qualitatively similar to T/B monoclonal mice, although displaying lower overall IgE values.
We also investigated whether cells with Treg phenotypes induced after i.p. immunization could suppress the Th2/IgE response. We purified CD25+ cells from T/B monoclonal mice that had either been immunized i.p. with OVA-HA (Imm group) or had received OVA orally and subsequently been immunized i.p. with OVA-HA (Tol group). In both groups cell purification was performed 10 days after i.p. immunization. A total of 5 x 105 CD4+CD25+ T cells were transferred to naive T/B monoclonal mice, and the mice were immunized i.p. 1 day later with OVA-HA in alum. As shown in Figure 7C, cells from both the Imm- and the Tol-group mice efficiently suppressed the IgE response. Thus, both oral administration of antigen and i.p. immunization with adjuvant induce functional Tregs, but in the latter case, Treg development does not occur sufficiently early to affect the course of the concomitant Th2 response.
IL-10 is not necessary for the induction of oral tolerance in T/B monoclonal mice.
The mechanism of suppression by naturally occurring Tregs in vitro is cell-contact dependent and cytokine independent whereas the cytokines IL-10 and TGF- have been shown to be important for in vivo suppression in several experimental models (44-46). In addition, both IL-10 and TGF- were found to have the ability to induce Treg activity in vitro. While TGF- has been implicated in oral tolerance, the role of IL-10 in oral tolerance is controversial (4, 47, 48). We next investigated to determine whether IL-10 and TGF- are required for induction of oral tolerance in the absence of thymus-derived Tregs.
IL-10–deficient T/B monoclonal mice were generated by crossing T/B monoclonal mice with BALB/c IL-10–/– mice. As shown in Figure 8, IL-10–/– T/B monoclonal mice developed hyper–IgE response and airway inflammation after i.p. immunization and respiratory challenge. However, when compared to that in IL-10+ T/B monoclonal mice (Figures 1 and 2), serum IgE and eosinophilia in IL-10–/– T/B monoclonal mice were modestly but reproducibly reduced. Oral OVA administration before i.p. immunization resulted in suppression of all asthma parameters analyzed, namely BAL eosinophilic infiltrate, lung inflammation, and mucus secretion (Figure 8, A and C). Interestingly, neutrophilic infiltration was not reduced in Tol group IL-10–/– T/B monoclonal mice, probably because lung neutrophilic infiltration is mediated by Th1 cells (49-51). From the early days of IL-10 research, it has been known that IL-12 and IFN-, 2 critical cytokines in Th1 biology, are targets of IL-10 inhibition (52). Thus, it is not surprising that this particular aspect of lung inflammation is not significantly reduced in Tol group T/B monoclonal IL-10–deficient mice.
IL-10–/– T/B monoclonal mice of the Tol group displayed strong inhibition of B cell responses, such as the production of IgG1 and IgE (Figure 8B) and GC reaction (Supplemental Figure 5A). Like tolerance induction in IL-10+ T/B monoclonal mice, that in IL-10–/– mice was accompanied by a lower accumulation of CD45RBlowCD25– (effector/memory T cells) cells (Supplemental Figure 5B). IL-10–/– T/B monoclonal mice were also susceptible to nasal tolerance (Supplemental Figure 6). Thus, in this experimental system, IL-10 is not necessary either for the development of the asthmatic response or for the establishment of effective mucosal tolerance.
TGF- is required for oral tolerance in T/B monoclonal mice.
We tested next to determine whether TGF- was required during the initial oral tolerization phase. To this end, we injected T/B monoclonal mice with the depleting anti–TGF- antibody 1D11 before, during, and immediately after oral OVA administration. As shown in Figure 9, neutralization of TGF- impaired oral tolerization, reverting suppression of eosinophilic airway inflammation, production of IL-4 by cells in BAL, and production of seric IgG1 and IgE (Figure 9, A–C). We also observed a reversion of the suppression of GC formation (Supplemental Figure 7A) and of the development of CD45RBlowCD25– T cells (Supplemental Figure 7B).
To determine the role of TGF- in the in vivo differentiation of Tregs during OVA feeding, we administered anti–TGF- antibody 1 day before and 2 days after the beginning of oral treatment. On day 5 of oral treatment (Figure 1A; day –2), we analyzed the expression of CD25 and CD45RB in mLN cells. We observed an increase in CD45RBlowCD25+ cells (as well as in recently activated CD45RBhiCD25+ cells) in mice that received OVA orally compared with untreated T/B monoclonal mice (Figure 10A). The same analysis enabled us to confirm that, as expected, unimmunized T/B monoclonal mice have no CD45RBlowCD25+ cells, the region in the FACS plot in which Tregs are found (Figure 10A). Anti–TGF- treatment resulted in only a moderate reduction of the CD45RBlowCD25+ population (Figure 10A). In order to determine Foxp3 expression levels, we FACS-sorted the 4 populations defined by anti-CD45RB and anti-CD25 antibodies from mLNs and prepared cDNA for real-time PCR analysis. As anticipated, only CD45RBlowCD25+ cells expressed Foxp3. Importantly, anti–TGF- treatment resulted in a 2- to 3-fold reduction of Foxp3 expression in mLN cells (Figure 10B). The reduction in Foxp3 expression was even more marked in spleen cells (Supplemental Figure 8).
Figure 10
Neutralization of TGF- in vivo inhibits early Foxp3 expression. T/B monoclonal mice were injected with anti–TGF- 1 day before and 3 days after the beginning of administration of 1% OVA in the drinking water. After 5 days of oral-OVA, CD4+ mLN cells were analyzed for expression of CD45RB and CD25 by FACS and for expression of Foxp3 by real-time PCR. (A) mLN cells from mice that received oral-OVA alone, from mice that received anti–TGF- antibodies and oral-OVA, and from untreated T/B monoclonal mice were stained with antibodies for CD4, CD45RB, and CD25. The figure shows representative plots of CD4+ gated cells. (B) CD4+ cells from pooled mLN (4 mice per group) were sorted in a MoFlo flow cytometer into CD45RBlowCD4+CD25+, CD45RBlowCD4+CD25–, CD45RBhiCD4+CD25+, and CD45RBhiCD4+CD25– fractions. Foxp3 expression in the samples was determined by real-time PCR. Results are expressed as mean ± SD of triplicate wells.
Our results are consistent with the notion that oral antigen administration induces antigen-specific Tregs in a process that requires TGF- for full Foxp3 induction. Our results from the adoptive transfer experiments strongly support the notion that antigen-specific Tregs induced by oral tolerance prevent asthma-type responses by inhibiting Th2 differentiation and class switching to IgE in the lymphoid organs.
Discussion
In this manuscript, we make 2 main observations. The first is that oral tolerance can be induced in the absence of thymic-derived Tregs. Establishment of oral tolerance correlates with the de novo induction of antigen-specific CD4+CD25+Foxp3+ Tregs, which is impaired when TGF- is blocked. Second, we show that a single immunization with antigen plus adjuvant leads to the generation of functional antigen-specific Tregs, which, in this case, occurs in parallel with the generation of effector Th2 cells.
Several mechanisms have been proposed to account for oral tolerance, such as clonal deletion of antigen-specific T cells, immune deviation, T cell anergy, and the induction of Tregs (4, 47, 53). In fact, the transfer of tolerance by Tregs obtained from animals that have been fed antigen has been known for more than 25 years (54, 55). It has been shown, using OVA-specific DO11.10 TCR transgenic mice, that in tolerant mice there is an increase in the CD4+CD25+ population. These CD25+ cells prevented a delayed type hypersensitivity response upon transfer into BALB/c mice (56). Several groups have used adoptive transfer of DO11.10 OVA-TCR transgenic T cells into wild-type animals to demonstrate the induction of CD4+ cells that are able to transfer tolerance (11, 14, 57). Recently, Ostroukhova et al. (17) described Foxp3 expression in antigen-stimulated cultures of membrane TGF-+CD4+ T cells from mice tolerized to OVA by respiratory antigen exposure. Stock et al. showed that splenic CD8+ DC from mice tolerized to OVA through the airways induced antigen-specific Tregs that expressed Foxp3, Tbet, IFN-, and IL-10 (23). In these and other studies, a direct or inductive role for thymus-derived Tregs in antigen-specific tolerance could not be ruled out.
To clarify in a definitive manner the need for thymus-derived Treg cells in oral tolerance, we studied mucosal tolerance in mice that lack naturally occurring thymus-derived Tregs (Figure 10A) and showed that oral administration of OVA previous to i.p. immunization with OVA-HA dramatically suppressed an asthmatic inflammatory response in these mice.
We also observed that tolerance was associated with the induction of antigen-specific CD4+CD25+ cells that expressed markers of naturally occurring Tregs, such as Foxp3 and CTLA-4 (13, 41-43). CD4+CD25+ cells induced by oral antigen administration behaved as naturally occurring Tregs, as they were anergic and suppressive upon stimulation with anti-CD3 antibodies in vitro. Importantly, transfer of these cells led to suppression of the IgE response. Thus, oral delivery of antigen induced antigen-specific naive CD4 cells to become Tregs by a process that is independent of the presence of thymic-derived Tregs. Although we did not formally exclude the possibility that orally administered OVA makes its way to the thymus and promotes the development of immature cells into Tregs, we believe that this possibility is unlikely given the relatively rapid appearance of CD25+Foxp3+ cells (Figure 10, A and B) and recent reports demonstrating antigen-induced generation of Tregs in thymectomized animals (20) and the conversion of naive mature peripheral CD25–Foxp3– T cells into Tregs in a transfer system (22).
The generation of antigen-specific Tregs by oral administration of antigen explains the discrepancies between our conclusions and those of Dubois and coworkers (16). These authors concluded that naturally occurring Tregs are required for oral tolerance. They antibody-depleted CD25+ cells in B6 mice and showed that oral tolerance was abrogated. However, since the last antibody treatment was performed 7 days after the oral feeding, it is likely that the authors depleted not only the naturally occurring Tregs but also those Tregs that had been peripherally generated by the oral feeding.
Recently, Apostolou and von Boehmer showed that continuous subcutaneous antigen delivery induced Foxp3+ Tregs that were indistinguishable from naturally occurring Tregs (20). Our results extend those of Apostolou and von Boehmer by demonstrating that antigen-specific Tregs can be induced by mucosal delivery of antigen. Importantly, we found that a single parenteral immunization in the presence of antigen also induced Treg development. In this case, however, Tregs were induced concomitantly to Th2 cells.
If antigen-specific Tregs can be generated upon single immunization even in the presence of adjuvant, one may wonder why these Treg do not control the primary immune response. In fact, as we previously reported, T/B monoclonal mice develop hyper-Th2 and hyper-IgE responses after a single immunization, indicating lack of regulation. The explanation is provided by our kinetic data (Figures 4, 5, and 10), which show that high Foxp3 expression is attained only 10 days after a single i.p. immunization of T/B monoclonal mice. At this time, there is already a robust Th2 response. In order to inhibit Th2 differentiation and hyper-IgE production, regulation has to be in place before day 4 after immunization (Supplemental Figure 9), which is not the case during the normal course of the response in T/B monoclonal mice. However, while the Tregs generated by parenteral exposure to antigen in T/B monoclonal mice are not able to control the primary immune response, they may help downregulate further responses or reduce the damage caused by chronic antigenic stimulation. Accordingly, we observed that in T/B monoclonal mice repeatedly immunized i.p. with OVA-HA, there was an increase in Foxp3 levels and a decrease in IL-4 production by CD25– T cells (Supplemental Figure 10).
The role of IL-10 in mucosal tolerance is controversial (13, 17, 18, 58, 59). In the model of hyper-IgE and asthma described here, oral tolerance did not require IL-10, since IL-10–/– T/B monoclonal mice were as susceptible to oral tolerance as their IL-10+ littermates. However, neutrophilic inflammation was not ameliorated by oral tolerance in IL-10–/– mice.
The key role of TGF- in oral tolerance was established long ago (60, 61). In contrast, experiments with TGF-1–/– mice showed that oral tolerance could be achieved in the absence of TGF-1, although the degree of inhibition of the response by antigen feeding was much lower in TGF-1–/– mice than in TGF-1+ control mice (62). This experimental system was further complicated by anti–lymphocyte function-associated antigen-1–antibody (anti–LFA-1–antibody) treatment of the mice. In our experimental model, blockade of TGF- caused an almost complete reversal of the suppression of GC formation and memory T cell development while other parameters, such as eosinophilia and IgE production, were only partially, albeit significantly, reversed. At this time we do not know whether the residual suppression of IgE and eosinophilia was due to incomplete neutralization of TGF- or to the fact that a small fraction of the suppression operates via TGF-–independent mechanisms. For instance, the suppression of neutrophil numbers in BAL was not reversed by anti–TGF- antibodies, which is consistent with the fact the suppression of neutrophil migration may be dependent on IL-10.
It is not completely clear whether, in vivo, TGF- is an inductive stimulus for Treg generation, an effector molecule that mediates Treg suppressive function, or both. It has been proposed that oral administration of antigens induces Th3 cells. The TGF- produced by Th3 cells would be a major effector molecule in the suppression of responses (28). However, the role of TGF- in the induction of Th3 cells in the mucosa has not been determined. Our results show that blockade of TGF- in vivo abolishes oral tolerance and considerably impairs the induction of CD25+Foxp3+ Tregs. Given the lack of markers that uniquely identify Th3 cells, the relationship between the Foxp3+ cells that we describe here and Th3 cells has not been determined. However, oral tolerance in our model was not accompanied by enhanced concentration of active TGF- in the airways (data not shown), suggesting that, in this model, TGF- acts as an inductor of Tregs but not as an effector molecule in the suppression of asthma-like symptoms.
It has been shown that in vitro treatment of cells with TGF- induces regulatory cells that are more (21, 29, 31, 63) or less (64) similar to naturally occurring Tregs. Thus, our results confirm previous observations on the importance of TGF- in oral tolerance and extend those observations to include the differentiation of antigen-specific Foxp3+CD4+ Tregs in vivo upon oral administration of antigen.
The importance of TGF- in the generation of CD25+Foxp3+ Tregs in the periphery contrasts with the fact that naturally occurring Tregs can be generated in the absence of TGF-1 (65). Thus, although peripherally generated and thymic-derived naturally occurring Tregs have essentially the same phenotype and functional characteristics, they differ in the TGF- requirement for their generation. TGF- appears to have a role in the homeostasis of both naturally occurring and peripherally generated CD4+CD25+Foxp3+ Tregs (66-68). It is likely that a similar situation occurs for IL-2. IL-2 is not needed for the thymic generation of naturally occurring Tregs (22, 69, 70) but is required for the peripheral maintenance and function of naturally occurring Tregs and probably for the peripheral induction of Tregs (22, 69). It is evident now that Foxp3+CD25+ Tregs can be of thymic or peripheral origin and that additional factors are needed for the peripheral generation of Tregs that are not necessary for the generation of naturally occurring thymic-derived Tregs.
The fact that conventional immunization protocols lead to the generation of Tregs is of significance. Since, before i.p. immunization, naive OVA-specific T cells that will become Tregs cannot be distinguished from those that will become Th2 cells, it remains to be determined whether generation of Tregs versus that of effector T cells is a stochastic process or some microenvironmental conditions promote the development of one cell type over the other. The fact that mucosal administration of antigen promotes the development of Tregs with very little Th2 differentiation favors the second possibility.
Methods
Mice.
The T/B monoclonal mice (17/9 DO11.10 RAG1–/–) bearing monoclonal populations of T and B lymphocytes specific for chicken ovalbumin 323–339 and HA of influenza virus, respectively, were generated as previously described (32). BALB/c mice were purchased from Taconic or the Jackson Laboratory. BALB/c IL-10–/– mice were obtained from Donna Rennick (DNAX, Palo Alto, California, USA). TCR–/––/–, DO11.10 TCR–/––/–, and 17/9 DO11.10 RAG1–/– IL-10–/– mice (T/B monoclonal IL10–/– mice) were all backcrossed into a BALB/c genetic background for more than 10 generations. All IL-10–/– mice were kept on sulfamethoxazole (400 mg/l) and trimethoprim (80 mg/l) in their drinking water, except for the days in which they received OVA orally. All mice were bred and housed under specific pathogen-free conditions at the Skirball Institute animal facility. All procedures involving animals were approved by the New York University School of Medicine Institutional Animal Care and Use Committee.
Oral antigen administration, immunization, and airway challenge.
Oral tolerance to OVA was induced by offering to the animals, ad libitum, a 1% OVA (grade II; Sigma-Aldrich) solution dissolved in drinking water for 5 consecutive days. The HA peptide (YPYDVPDYASLRS) was synthesized by ResGen. Crosslinked OVA-HA was prepared as previously described (32). Immunization with OVA-HA was performed i.p. with 100 μg of OVA-HA adsorbed to 1 mg of alum, 2 days after the end of the oral treatment. To induce airway inflammation, anesthetized mice were administered 10 μg of OVA-HA i.n. in 50 μl of PBS (25 μl in each nostril) on days 14 and 21 after i.p. immunization. For TGF- neutralization, mice were injected i.p. with 2 mg of the anti–TGF- monoclonal antibody 1D11 on 1 day before and 2, 5, and 8 days after the beginning of oral treatment.
BAL collection and lung histology.
Mice were deeply anesthetized by i.p. injection of anesthetic solution containing ketamine and xylazine. The tracheae were cannulated, and lungs were lavaged twice, once with 0.5 ml and once with 1.0 ml PBS. After total cell counting, cytospin preparations of the BAL cells were stained with DiffQuik (Baxter Dade AG), and differential cell counts were performed on 200 cells on the basis of morphology and staining characteristics. Student’s t test was used for statistical analysis.
Lungs were removed after BAL collection, perfused via the right ventricle with 10-ml saline to remove residual blood, fixed with phosphate-buffered formalin, and embedded in paraffin. Tissue sections were stained with H&E to determine cellular inflammation or with PAS/hematoxylin for evaluation of mucus-producing cells.
Serum and BAL antibodies.
Total and HA-specific antibodies in serum or BAL samples were quantified by ELISA as described (32). Purified and biotinylated antibodies to Ig isotypes and standard purified immunoglobulin isotypes were purchased from BD Biosciences — Pharmingen and CALTAG Laboratories. Serum titer was defined as the lowest dilution that rendered an OD value higher than 0.1 after background subtraction.
FACS analysis.
Single cell suspensions in staining buffer (PBS containing 2% fetal calf serum and 0.1% NaN3) were incubated for 45 minutes at 4°C with the antibody cocktails. Samples were analyzed in a FACSCalibur instrument (BD). FITC-labeled and biotin-labeled HA peptides were purchased from ResGen. Peanut agglutinin–FITC and peanut agglutinin–biotin were purchased from Vector Laboratories. The remaining antibodies were purchased from BD Biosciences — Pharmingen and CALTAG Laboratories.
Cytokine production ex vivo.
Cytokine production was analyzed ex vivo by intracellular staining. Briefly, cells were stimulated with 1-μM OVA 323–339 peptide for 4 hours. During the last 2 hours, cells were incubated with monensin (Sigma-Aldrich) to inhibit secretion. Cells were then surface stained with FITC-labeled KJ1–26 and PerCP-labeled anti-CD4 antibodies, fixed, permeabilized, stained with PE-labeled anti–IL-4 antibodies, and analyzed in a FACSCalibur.
Cell purification and transfer.
CD4+CD25+ and CD4+CD25– lymphocytes were purified from spleen and mLN cells by magnetic sorting using Miltenyi Biotec reagents and VarioMACS apparatus as described (22). Cell purity was checked by FACS analysis. The CD25+ purified fraction contained no more than 3% CD4+CD25– contamination. Purified CD25– cells contained 0.5–2% of CD25low cells and no CD25high cells. 3–5 x 105 purified cells were injected i.v. into recipient mice. In some experiments, CD4+CD25+ and CD4+CD25– cells were sorted in a MoFlo apparatus at the NYU Sorting Facility.
RNA analysis.
For quantitative mRNA expression analysis, CD4+CD25– and CD25+ cells were purified using either magnetic sorting or MoFlo sorting as described (22). RNA was extracted from samples using TRIzol (Invitrogen Corp.), and cDNA was synthesized by standard procedures. The expression of Foxp3, CTLA-4, IL-4, IFN-, and -actin was determined by quantitative real-time PCR. Primers for Foxp3, CTLA-4, and -actin were as described (22). Other primer sequences are as follows: IL-4: ACAGGAGAAGGGACGCCATG and GCAGCTTATCGATGAATCCA; IFN-: GCTTTGCAGCTCTTCCTCAT and TCTTCCACATCTATGCCACTTG; TGF-: CTGCTGACCCCCACTGATA and GCTGAATCGAAAGCCCTGTA; SMAD2: CCGGCTGAACTGTCTCCTAC and ATAGTATGCGATTGAACACCAGAATG; IL-10: TCCCCTGTGAAAATAAGAGCA and TGGCCTTGTAGACACCTTGG; and IL-5: AGCAATGAGACGATGAGGC and ACACTTCTCTTTTTGGCGGT.
In vitro suppression assay.
CD4+CD25– and CD25+ cells from T/B monoclonal mice as well as fresh BALB/c CD4+CD25– and CD25+ cells were purified using magnetic sorting. Proliferation assays were set up in 96-well round bottom plates and contained, per well, the following: 2 x 104 responder cells (CD4+CD25– BALB/c cells); 4 x 104 APCs (mitomycin C–treated spleen cells from TCR-deficient BALB/c mice); and anti-CD3 antibody at a concentration of 0.5 mg/ml. Putative suppressor cells were cocultured at responder/suppressor ratios of 1.0:1.0, 1.0:0.3, and 1.0:0.1. Proliferation was determined by adding 3H-thymidine on the third day of culture and determining incorporation 6 hours later.
Acknowledgments
Work in the J.J. Lafaille laboratory is supported by the NIH/National Institute of Allergy and Infectious Diseases, the National Multiple Sclerosis Society, and the Dana-Goldsmith Foundation. D. Mucida was a recipient of a predoctoral fellowship from Coordenaao de Aperfeioamento de Pessoal de Nivel Superior, Brazil. D. Mucida would like to thank Ana M.C. de Faria, Nelson M. Vaz, and A.C. Keller for very helpful discussions and suggestions.
Footnotes
Nonstandard abbreviations used: BAL, bronchoalveolar lavage; CTLA-4, cytotoxic T lymphocyte–associated antigen 4; GITR, glucocorticoid-induced TNF receptor; GC, germinal center; Imm, mice given OVA-HA i.p. immunization; mLN, mesenteric lymph node; Oral, mice fed OVA in drinking water; RAG, recombination activating gene; Th3 cell, TGF-–producing Treg cell; Tol, mice fed OVA in drinking water prior to OVA-HA i.p. immunization.
Conflict of interest: The authors have declared that no conflict of interest exists.
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