Blocking CD27-CD70 Costimulatory Pathway Suppresses Experimental Colitis

Monika Manocha, Rietdijk Svend, Amale Laouar, Gongxian Liao, Atul Bhan, Jannine Borst, Cox Terhorst and N. Manjunath
J Immunol July 1, 2009, 183 (1) 270-276; DOI: https://doi.org/10.4049/jimmunol.0802424

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Abstract

The pathogenesis of human inflammatory bowel disease (IBD) and most experimental models of IBD is dependent on the activation and expansion of CD4+ T cells via interaction with mucosal APCs. The costimulatory receptor CD70 is transiently expressed on the surface of conventional dendritic cells, but is constitutively expressed by a unique APC population in the intestinal lamina propria. We used two experimental IBD models to evaluate whether interfering the interaction between CD70 and its T cell ligand CD27 would affect the development of colitis. Adoptive transfer of naive CD27-deficient CD45RBhigh CD4+ T cells into Rag-1−/− mice resulted in significantly less disease than when wild-type CD45RBhighCD4+ T cells were used. Moreover, a monoclonal anti-CD70 Ab prevented the disease caused by the transfer of wild-type CD45RBhigh CD4+ T cells into Rag-1−/− mice and the same Ab also ameliorated an established disease. The colitis associated proinflammatory cytokines IL-6, TNF-α and IFN-γ were significantly reduced after anti-CD70 Ab treatment, suggesting an overall reduction in inflammation due to blockade of pathogenic T cell expansion. Anti-CD70 Ab treatment also suppressed trinitrobenzene sulfonic acid-induced colitis in SJL/J mice. Because anti-CD70 Ab treatment suppressed multiple proinflammatory cytokines, this may be a more potent therapeutic approach for IBD than blockade of individual cytokines.

Inflammatory bowel disease (IBD)3 is a chronic inflammatory disorder of the gastrointestinal tract that occurs in immunocompetent individuals and is characterized by an aberrant mucosal T cell-mediated inflammation (1, 2). Despite intensive study of IBD pathogenesis, the initiating Ags and the mechanisms that sustain the inflammatory process remain incompletely understood (3, 4). Interaction of the T cell-expressed TNF receptor family of costimulatory molecules with their respective TNF-related ligands found predominantly on APCs play a critical role during T cell activation and differentiation (5, 6, 7, 8). The role of many TNF family members in IBD has been well studied in experimental models and TNF Ab is also being used to treat human IBD (9, 10). Many recent studies have also shown that interaction of the costimulatory molecule CD27 with its ligand CD70 plays a key role in the expansion and survival of Ag-activated T cells (11, 12, 13). However, the role of this pathway in IBD has not been studied.

In both mice and humans, CD27 is constitutively expressed on naive and memory T cells as well as on subsets of activated B cells, NK cells, and hematopoietic progenitor cells (11). In contrast, the expression of its ligand CD70 is tightly regulated (14). CD70 is absent on quiescent T, B, and dendritic cells, but can be induced transiently on T cells after activation and on dendritic cells after stimulation with anti-CD40 or LPS (15, 16). Interaction of CD27 with CD70 appears to be important for an effective T cell response in vivo because CD27-deficient mice generate lower numbers of effector CD4 and CD8 T cells in response to a viral infection compared with wild-type (wt) mice (17). Similarly, administration of recombinant soluble CD70 protein during Ag stimulation enormously enhances the T cell response in vivo (18). However, unchecked expression of CD70 predisposes to immunopathology. Aberrant expression in CD70 transgenic mice results in massive activation of T cells responding to self-Ags, attended with depletion of naive T cell pool that eventually leads to immunosuppression (19). Soluble CD70 protein treatment also abrogates the requirement for adjuvants and prevents the tolerance induction observed with administration of Ag alone (18). Persistent CD70 expression also characterizes the human rheumatoid arthritis and systemic lupus erythematosis (20, 21). Thus, controlled expression of CD70 appears to be crucial for proper T cell activation and to prevent pathogenesis. By corollary, the CD27-CD70 costimulatory pathway may also provide an important target to prevent T cell-mediated immunopathology. Indeed, the beneficial effect of blocking this pathway with anti-CD70 Ab has been shown in animal models of cardiac allograft rejection and experimental autoimmune encephalomyelitis (22, 23).

We have previously reported that a novel type of APCs in the mouse intestinal lamina propria constitutively express CD70 and critically contributes to the mucosal T cell expansion in response to an oral infection (24). In the present study, we analyzed the role of CD27-CD70 interaction in IBD using two murine experimental models of colitis. Our results suggest that CD27-CD70 interaction is critical to sustain T cell-mediated intestinal inflammation and blocking this pathway may provide a potential tool for therapeutic intervention in IBD.

Materials and Methods

Mice

C57BL/6, Rag-1−/−, and SJL/J mice were purchased from The Jackson Laboratory. CD27-deficient mice on C57BL/6 background has been described (17). All mice were maintained in the specific pathogen-free animal facility at the Immune Disease Institute (IDI) and were used when they were 4–6 wk of age. All animal experiments had been approved by the Institutional Review Board of IDI.

Ab treatment

In the T cell transfer model, wt CD4+CD45RBhigh T cell-transferred Rag-1−/− mice were injected i.p with 500 μg of anti-CD70 Ab (clone 3B9) (14) or control hamster IgG (Jackson Immunoresearch Laboratories) twice a week starting from the day of adoptive transfer or 3 or 5 wk after transfer. In the trinitrobenzene sulfonic acid (TNBS) model, the Abs were administered on the day of TNBS injection and repeated 2 and 4 days later. In the innate colitis model, hamster IgG or anti-CD70 Abs were injected 4 h before injecting anti-CD40 and repeated on days 2 and 4.

Flow cytometry and cell sorting

FITC-, PE-, or PerCP-conjugated Abs to mouse CD4, CD45RB, CD8, CD27, and CD70 were from BD Pharmingen. Immunostaining and flow cytometric analysis were done as described earlier (24) using FACScan flow cytometer. Cell sorting was done using a FACSAria Sorter (BD Biosciences).

T cell transfer colitis

Naive CD4+CD45RBhigh T cells were isolated from the spleens of naive C57BL/6 wt mice or CD27-deficient mice by cell sorting. After confirming that the isolated cells were >95% pure, 5 × 105 sorted cells were suspended in 200 μl of sterile PBS and injected i.p. into Rag-1−/− recipient mice of same age and sex as the donor mice. The recipient Rag-1−/− mice were weighed initially and then weekly after cell transfer. All mice were sacrificed when signs of diarrhea, hunching, and wasting disease appeared in the control hamster IgG-treated mice. Mice were monitored for colitis as described previously (25). In brief, disease activity index (DAI) was compiled as sum of four parameters: hunching and wasting were scored 0 or 1, stool consistency 0–3, and colon thickening 0–3 with higher scores representing more severe colitis. Histological colitis scores were obtained using tissue samples from the proximal, middle, and distal colon. The histology scores were assigned in a blinded manner by our participating pathologist, Dr. A. K. Bhan. The sections were scored for the presence of crypt abscesses (0–1), the degree of mucosal thickness (0–3), and the degree of inflammatory infiltrate (0–3). The maximum score for DAI was 8 and for histological index it was 7.

TNBS colitis

Colitis was induced in SJL/J mice as described by Neurath et al. (26). Mice were anesthetized with i.p. injection of ketamine/xylazine and 0.5 mg of TNBS (Sigma-Aldrich) in 25% ethanol (150 μl) administered intrarectally through a catheter inserted 4 cm deep from the anus. Animals were then kept in a vertical position for 30 s and returned to their cages. Control animals received 150 μl of 25% ethanol. All mice were weighed before disease induction and every day thereafter until sacrifice on day 7. On day 7, DAI and histology scores were measured as described earlier except that the following criteria were used for histological scoring: ulceration (0–2+); inflammatory infiltrate (0–3+); edema (0–2+); crypt abscess (0–1+); goblet cell depletion (0–1+); and mucosal thickening (0–3+), with the maximum histological colitis score of 12.

Innate immune colitis

Age and sex-matched Rag-1−/− mice were injected i.p. with 200 μgs of an agonistic CD40 mAb (FGK45) (27) or with isotype control (Rat IgG2a). All mice were weighed daily and monitored for colitis as described in the T cell transfer model.

Isolation of lamina propria mononuclear cells

The lamina propria lymphocytes were isolated from whole colons as described earlier (24). In brief, the excised colons were cut longitudinally, washed thoroughly, and cut into ∼5 mm pieces. The pieces were transferred to a 50-ml tube containing 10 ml of CMF-FBS-EDTA solution (CMF-HEPES solution with 10% FBS, 5 mM EDTA, and 100 μg/ml gentamicin). The tubes were shaken in a magnetic stirrer for 20 min at room temperature, the supernatant collected, and the EDTA treatment repeated two more times. Finally, the colonic tissue was washed in tissue culture medium (to remove residual EDTA) and digested with 300 U/ml collagenase (type VIII; Sigma-Aldrich) at 37°C for 1 h with shaking. The supernatants were passed through a 70-μm nylon wool strainer and lamina propria lymphocytes were harvested by Percoll gradient centrifugation.

Cytokine analysis

Lymphocytes from the mesenteric lymph node (MLN) of T cell-transferred mice were isolated and 2 × 105/ml cells were stimulated with plate-bound anti-CD3ε Ab (10 μg/ml, 145–2C11; eBioscience) in triplicates in 96-well plates. After 48 h of culture, supernatants were harvested and stored at −20°C for cytokine analysis. For colon explant cultures, small pieces of the colonic tissue samples (∼5 mm of mid-colon weighing 100 mgs each) were washed extensively and cultured in 500 μl of tissue culture medium in 24-well plates at 37°C overnight. The culture medium was centrifuged and the supernatants were stored for analysis. Cytokine levels were quantitated using the cytometric bead array (CBA kit, BD Biosciences) according to the manufacturer’s instructions and data analysis was performed using the BD CBA software.

Statistical analysis

Nonparametric data were analyzed using two tailed Mann-Whitney U test (DAI and histological data). Levels of cytokine are presented as the mean ± SEM. These data were analyzed by the Student’s t test. p ≤ 0.05 was considered statistically significant and the statistical analysis was done with Graph Pad Prism 4.00 (GraphPad).

Results

Blockade of CD70 or absence of CD27 prevents the induction of colitis in the CD45RBhigh CD4+ T cell ⇒ Rag-1−/− transfer model

Adoptive transfer of wt CD4+CD45RBhigh naive T cells into SCID or Rag-1−/− mice leads to weight loss, diarrhea, and severe colitis in 6–8 wk (28). Hence, we used this model to test the importance of CD27-CD70 costimulatory pathway in the mucosal T cell-mediated pathology. We transferred sorted CD45RBhighCD4+ T cells (5 × 105 cells/mouse) isolated from either wt or CD27-deficient mice into Rag-1−/− mice. The wt CD45RBhighCD4+ T cell-transferred recipient mice were either treated with a control hamster IgG or anti-CD70 Ab (500 μg/mouse by i.p. injection twice weekly starting at the time of T cell transfer). The mice were monitored for weight loss and clinical symptoms of colitis over time. Eight weeks after transfer, when the recipient mice treated with the control hamster IgG developed a moderate to severe colitis, all mice were scored for disease activity, the mice sacrificed, and their colonic tissues histologically examined. Rag-1−/− recipient mice transferred with wt CD45RBhighCD4+ T cells and treated with hamster IgG showed a progressive weight loss and developed clinical disease by 8 wk. In contrast, wt CD45RBhighCD4+ T cell-transferred recipient mice treated with anti-CD70 Ab as well as Rag-1−/− mice transferred with CD27-deficient T cells, showed significantly less weight loss and disease activity (Fig. 1⇓, A and B). Histological examination of colonic sections in Hamster IgG-treated mice showed a transmural inflammation with mononuclear cell infiltration in the lamina propria and prominent epithelial hyperplasia with loss of goblet cells. These features were much less evident in the anti-CD70 Ab-treated mice as well as in mice transferred with CD27-deficient T cells (Fig. 1⇓, C and D). Moreover, a quantitative evaluation of the CD4+ T cell infiltrates, measured by flow cytometric analysis of isolated lamina propria mononuclear cells, revealed significantly reduced CD4 T cell numbers in anti-CD70 Ab treated mice compared with hamster IgG treated mice (0.8 ± 0.08 × 106 and 0.15 ± 0.6 × 106 respectively, for control and anti-CD70 Ab-treated mice, measured at 8 wk after transfer; n = 5, p < 0.05). Thus, CD27-CD70 costimulation appears to be important for sustaining T cell mediated intestinal inflammation.

FIGURE 1.
FIGURE 1.

CD27-CD70 interaction is required for the development of colitis in the T cell transfer model. Rag-1−/− mice were transferred with CD4+CD45RBhigh CD4 T cells from wt or CD27-deficient mice and the wt T cell transferred mice treated with control hamster IgG or anti-CD70 Ab. Induction of colitis was assessed 8 wk after transfer. Weight loss (A), disease activity index (DAI) (B) and histology score (C). The data shown are pooled from three independent experiments with a total of 17–25 mice in each group. Each symbol represents an individual mouse and the horizontal line represents the median value. D, One representative histology slide from each of wt CD45RBhigh CD4 T cells transferred mice treated with hamster IgG (histology score = 7) or anti-CD70 Ab (histology score = 1) and CD27-deficient CD45RBhigh CD4 T cells transferred mice (histology score = 2) is shown (magnification, ×10). Colon sections from unmanipulated wt C57/BL-6 and Rag-1−/− mice are shown in supplementary Fig. S4.

We also analyzed the cytokine production by colonic tissue and MLN in Rag-1−/− recipient mice 8 wk after T cell transfer. For analysis of colonic samples, equivalent-sized colonic tissue was incubated with tissue culture medium overnight and supernatants collected for the cytokine assay. MLN cells (1 × 105/ml) were stimulated with anti-αCD3 (10 μg/ml) and culture supernatants collected after 48 h of culture. IFN-γ, TNF-α, and IL-6 levels were tested by CBA. Compared with the wt T cell-transferred Rag-1−/− recipient mice treated with hamster IgG, which showed highly elevated levels of these cytokines, cytokine levels were significantly reduced in the colon and MLN of both CD27-deficient T cell-transferred mice and anti-CD70 Ab-treated wt T cell-transferred mice (Fig. 2⇓, A and B). Collectively our results suggest that CD27-CD70 costimulatory pathway plays an important role in the development of colitis and blockade of this pathway suppresses the pathogenic T cell expansion attended by reduced production of inflammatory cytokines and intestinal inflammation.

FIGURE 2.
FIGURE 2.

Decreased cytokine production in the absence of CD27-CD70 interaction. Cytokine concentration in mice in Fig. 1 was measured in colon explant cultures (A) or MLN T cell cultures (B) using a CBA kit (n = 5–18 mice per group). The bar graphs represent mean values ± SD.

Anti-CD70 Ab therapy ameliorates an established colitis

Our preceding results show that blocking CD27-CD70 costimulation prevents the development of colitis. However, it was not clear whether this costimulatory pathway is only involved during the priming phase of the response or is important throughout the course of the disease. Only in the latter case would anti-CD70 Ab have a therapeutic potential. Although for CD8+ T cells, CD27-CD70 interactions appear to regulate expansion at the site of priming as well as expansion and survival at effector sites, this is much less clear for CD4+ T cells. Therefore, we tested the effect of anti-CD70 Ab treatment started after initiation of the disease in the Rag-transfer model.

In the preventive studies described earlier, weight loss in the hamster IgG treated mice started at ∼3 wk and clinical symptoms started to appear by 5 wk. Thus, we compared the anti-CD70 Ab treatment started from the day of transfer to that initiated 3 or 5 wk after the transfer of wt CD45RBhighCD4+T cells into Rag-1−/− recipients. Mice received 500 μg of hamster IgG or anti-CD70 Ab twice a week starting on the day of transfer or 3 wk or 5 wk after cell transfer. The mice were observed for weight loss and mortality until 12 wk. The hamster IgG-treated mice showed progressive weight loss, developed clinical symptoms, and 90% of the animals died by 12 wk. In contrast, animals treated with anti-CD70 Ab starting on the day of transfer or after 3 wk of transfer did not show significant weight loss and >90% of animals survived for the 12 wk period of observation (Fig. 3⇓, A and B). The wt T cell-transferred Rag-1−/− recipient mice that had started losing weight 5 wk after transfer, started to regain body weight after initiation of anti-CD70 Ab treatment, and 70% of animals survived during the 12-wk period of observation (Fig. 3⇓, A and B). Clinical and histopathological examination in the surviving mice showed that compared with hamster IgG-treated mice shown in Fig. 1⇑ (colonic sections were not taken from Hamster IgG treated mice in this experiment because most of the animals died during the extended observation period), much less inflammation was seen in the colons of anti-CD70 Ab-treated mice (Fig. 3⇓, C–E). Thus, CD70 blockade appears to be capable of reversing an established colitis.

FIGURE 3.
FIGURE 3.

Anti-CD70 Ab therapy ameliorates an established colitis. Wt CD45RBhigh CD4 T cell-transferred Rag-1−/− mice were treated with a control hamster IgG or anti-CD70 Ab starting from the day of transfer or 3 or 5 wk after T cell transfer. Severity of colitis was assessed by weight loss as a percentage of the starting weight (A), survival rate percentage (B), disease activity index (C), and histology score (D) (n = 5–7 mice per group). Data represent the mean values ± SD. ∗, p < 0.05. E, One representative histology slide from hamster IgG control and each treatment group (anti-CD70 Ab treatment initiated on day 0 and 3 and 5 wk after transfer) is shown (magnification, ×10).

Anti-CD70 Ab treatment also inhibits TNBS-induced colitis

To further confirm the importance of CD27-CD70 pathway in the intestinal T cell response, we also tested the ability of anti-CD70 Ab to reduce inflammation in the TNBS model of colitis. Intrarectal administration of TNBS in certain strains of mice results in a Th1 T cell-mediated transmural infiltrative colitis (29). Thus, groups of SJL/J mice were injected intrarectally with 0.5 mg of TNBS in 25% ethanol or 25% ethanol alone for nonspecific toxicity control. TNBS administered mice were i.p. injected with control hamster IgG or anti-CD70 Ab on days 0, 2, and 4. By day 7, the hamster IgG-treated mice had lost weight and showed clinical symptoms, whereas the anti-CD70 Ab treated and ethanol alone-injected mice did not lose weight or develop clinical symptoms (Fig. 4⇓, A and B). Correspondingly, the colonic histopathology was also significantly reduced after anti-CD70 Ab treatment when compared with hamster IgG treated mice, which showed depletion of goblet cells, hemorrhagic necrosis, ulceration, and transmural infiltration of mononuclear cells (Fig. 4⇓, C and D). These results confirm that anti-CD70 Ab blockade reduces the T cell-mediated immunopathology, irrespective of the method of induction of colitis.

FIGURE 4.
FIGURE 4.

Anti-CD70 Ab treatment prevents TNBS-induced colitis. SJL/J mice were injected intrarectally with 25% ethanol alone or with TNBS in 25% ethanol and treated with control hamster IgG or anti-CD70. Induction of colitis was assessed by weight loss as a percentage of the starting weight (A), DAI (B), and histology score (C). D, One representative histology slide from each treatment group of mice is shown (magnification, ×10).

Anti-CD70 Ab treatment does not inhibit non-T cell-mediated colitis

Although the effect of CD27-CD70 interaction on T cells is well studied, whether this interaction can also affect the CD70-expressing APC function remains largely unknown. Thus, a possibility existed that anti-CD70 Ab treatment could affect innate immunity by interfering with cytokine production by CD70-expressing macrophage/dendritic cells. Thus, we also tested anti-CD70 Ab in an innate immune model of colitis. Administration of an agonistic CD40 Ab to the T and B cell-deficient Rag-1−/− mice induces a rapid Th-1 cytokine-dependant systemic disease as well as an IL-23-dependant non-T cell-mediated colitis with myeloid cell infiltration of the colonic mucosa (27). Thus, we tested the effect of anti-CD70 Ab treatment in this model. Rag-1−/− mice were injected with 200 μg of anti-CD40 or an isotype control Ab once to induce the disease. The anti-CD40-injected mice were treated with control hamster IgG or anti-CD70 Ab on days 0, 2, and 4 after anti-CD40 injection and the mice were monitored for weight loss and disease development. Anti-CD70 Ab treatment failed to reduce either the systemic disease (rapid weight loss, spleen weight, and cellularity) (Fig. 5⇓, A–C) or the intestinal disease (DAI, histological score (Fig. 5⇓, D and E). In a separate experiment, we confirmed that CD70 is indeed induced on the splenic dendritic cells after treatment with anti-CD40 mAb treatment (supplementary Fig. S1).4 Taken together, these results suggest that CD70 blockade does not interfere with non-T cell mediated colitis.

FIGURE 5.
FIGURE 5.

Anti-CD70 Ab treatment does not inhibit non-T cell-mediated colitis. Rag-1−/− mice were injected with 200 μg anti-CD40 and treated with control hamster IgG or anti-CD70 Ab. Disease induction was assessed by weight loss (A), splenic weight (B), spleen total cell number (C), DAI (D), and histological score (E). Data represent the mean ± SD (n = 3 for isotype control (no anti-CD40) and n = 6 for anti-CD40 injected group).

Discussion

Our results suggest that CD27-CD70 costimulatory pathway plays an important role in the development of colitis and blockade of this pathway suppresses the pathogenic T cell accumulation in the gut mucosa attended by reduced intestinal inflammation and proinflammatory cytokine production.

Although the role of CD27-CD70 interaction in the differentiation and survival of CD8 T cells has been well studied, the role of this costimulatory pathway for CD4 T cells is less analyzed (30). Our results suggest that CD27-CD70 interaction is important for CD4 T cell activation in the intestinal mucosa. This is also consistent with studies showing the importance of this costimulatory pathway for the T cell response in the respiratory mucosa following influenza infection (31, 32). Indeed, although both CD28 and CD27 were required for priming a response to influenza virus in the lymph nodes, CD27 was more critical for the accumulation of virus specific T cells in the lungs (27). Thus, CD27-CD70 pathway may be particularly important in determining the expansion/survival of T cells at tissue sites of inflammation.

CD27-CD70 interaction appears to be particularly important to initiate a Th-1 pattern of differentiation for CD4 T cells with increased potential for IFN-γ and IL-2 production (30, 33). We also observed that the cytokines were significantly reduced after CD70 blockade. Considering that anti-CD70 Ab treatment failed to reduce inflammation in the innate model of colitis, the reduction in proinflammatory cytokines observed after anti-CD70 Ab treatment in the Rag-1−/− transfer model of colitis appears to be a consequence, rather than the cause for the reduction of T cell numbers.

It is noteworthy that the improvement in clinical and histological features of colitis was much more pronounced in the anti-CD70 Ab treated mice compared with CD27-deficient T cell transferred Rag-1−/− recipient mice. In addition to T cells, CD27 is also expressed by subsets of NK cells, and CD27high NK cells have lower activation threshold and secrete more cytokines than CD27low NK cells (34). Deliberate stimulation through this receptor is also known to augment inflammatory cytokine production by NK cells (35). Moreover, the NK cell numbers are significantly increased in the immunodeficient Rag-1−/− mice compared with wt mice (36). Because the CD27-CD70 pathway is only blocked on T cells after transfer of CD27-deficient T cells, whereas this pathway is also blocked in NK cells after anti-CD70 Ab treatment, it is possible that combined inhibition of T and NK cells after Ab treatment gave better protection compared with knocking out CD27 on T cells alone. However, it has been reported that NK cells can play a regulatory role in IBD since the colitis was augmented when IL-10-deficient or even sufficient CD4 T cells were transferred into NK cell-depleted Rag-1−/− mice (37). Thus, alternatively, compensatory mechanisms in CD27-deficient T cells or the presence of unidentified additional ligand(s) for CD70 may possibly account for the differences that we observed.

The fact that anti-CD70 Ab treatment could reverse the pathology even when administered after the disease has already become established suggests that continued CD27-CD70 interaction may be necessary to maintain the T cell-mediated inflammation and pathology of chronic colitis. These results are also consistent with earlier studies in the CD70 Tg mice. In CD70 Tg mice, both CD4 and CD8 T cells (responding to environmental or autoantigens) get profoundly activated (38) and sustained interaction of CD27-CD70 is necessary for this because treatment of 4-wk-old CD70 Tg mice with blocking CD70 Ab effectively reverses the phenotype (19). Although costimulation is generally thought to be important during APC-T cell interactions in the early stage of an immune response, APCs are also present at effector tissue sites and express costimulatory molecules. However, their role during chronic T cell activation is not well understood. Our results suggest that tissue-specific APCs may be necessary to maintain a sustained inflammation in the gut mucosa. Because CD70 is only transiently expressed by conventional dendritic cells, these cells are unlikely to be involved in the sustained activation of mucosal T cells during chronic colitis. In contrast, we have previously reported that a novel type of APC present exclusively in the intestinal lamina propria constitutively expresses CD70 (24). The CD70 expressing APC is also present in the Rag-1−/− mice (supplementary Fig. S2), as well as in SJL/J mice (data not shown). Although treatment with anti-human CD70 Ab is known to activate ADCC-mediated depletion of CD70 expressing tumor cells (39), Ab-mediated depletion of lamina propria effector T cells is unlikely to be the cause for protection against IBD because we did not observe significant CD70 expression by lamina propria T cells by flow cytometric examination either in wt mice or in our IBD models (Ref. 24 and data not shown). The fact that protection against IBD was also seen when CD27-deficient T cells were transferred to Rag-1−/− mice without Ab treatment also supports this hypothesis. Moreover, the anti-mouse Ab used in this (clone 3B9) appears to be nondepleting Ab in that the CD70+ APC were still present after Ab treatment (supplementary Fig. S3). Thus, it is likely that blockade of CD70 expressed on the CD70+ APC is the cause of protection induced by anti-CD70 Ab treatment in this study.

In summary, our results show that the CD27-CD70 costimulatory pathway is important in sustaining the T cell-mediated inflammation in IBD and blockade of this pathway may provide a tool for therapeutic intervention. The fact that continuous interaction of CD27/CD70 is necessary for the gut mucosal T cell expansion/survival is particularly important from a therapeutic viewpoint, because it would enable treatment after the disease is diagnosed. Because CD70 blockade directly leads to reduction in T cell numbers and thus reduce inflammation, this may provide a superior therapeutic approach for IBD than suppressing individual cytokines.

Acknowledgments

We acknowledge John Daley and Suzanne Dana for assistance in cell sorting, Haridas Viraga for providing help with anti-CD70 Ab generation, and Dorothy Vargas for animal care.

Disclosures

The authors have no financial conflict of interest.

Footnotes

  • The costs of publication of this article were defrayed in part by the payment of page charges. This article must therefore be hereby marked advertisement in accordance with 18 U.S.C. Section 1734 solely to indicate this fact.

  • ↵1 This work was supported by grants form the Crohn’s and Colitis Foundation of America (CCFA) and the Keef Foundation (to N.M.), and National Institutes of Health Grants DK47677 (A.K.B.), DK 52510 (C.T.) and the Center for the Study of Inflammatory Bowel Disease (DK43351) (to A.K.B. and C.T.).

  • ↵2 Address correspondence and reprint requests to Dr. N. Manjunath at the current address: Department of Biomedical Sciences, Paul L. Foster School of Medicine, Texas Tech University Health Sciences Center, 5001 El Paso Drive, El Paso, TX 79905. E-mail address: manjunath.swamy{at}ttuhsc.edu

  • ↵3 Abbreviations used in this paper: IBD, inflammatory bowel disease; wt, wild type; TNBS, trinitrobenzene sulfonic acid; MLN, mesenteric lymph node; DAI, disease activity index.

  • ↵4 The online version of this article contains supplemental material.

  • Received July 24, 2008.
  • Accepted April 30, 2009.

References

  1. ↵
    Fuss, I. J., M. Neurath, M. Boirivant, J. S. Klein, C. de la Motte, S. A. Strong, C. Fiocchi, W. Strober. 1996. Disparate CD4+ lamina propria (LP) lymphokine secretion profiles in inflammatory bowel disease: Crohn’s disease LP cells manifest increased secretion of IFN-γ, whereas ulcerative colitis LP cells manifest increased secretion of IL-5. J. Immunol. 157: 1261-1270.
    OpenUrlAbstract
  2. ↵
    Bouma, G., W. Strober. 2003. The immunological and genetic basis of inflammatory bowel disease. Nat. Rev. Immunol. 3: 521-533.
    OpenUrlCrossRefPubMed
  3. ↵
    Podolsky, D. K.. 2002. Inflammatory bowel disease. N. Engl. J. Med. 347: 417-429.
    OpenUrlCrossRefPubMed
  4. ↵
    Danese, S., C. Fiocchi. 2006. Etiopathogenesis of inflammatory bowel diseases. World J. Gastroenterol. 12: 4807-4812.
    OpenUrlPubMed
  5. ↵
    Cheuk, A. T., G. J. Mufti, B. A. Guinn. 2004. Role of 4-1BB:4-1BB ligand in cancer immunotherapy. Cancer Gene. Ther. 11: 215-226.
    OpenUrlCrossRefPubMed
  6. ↵
    Kwon, B., B. S. Kim, H. R. Cho, J. E. Park, B. S. Kwon. 2003. Involvement of tumor necrosis factor receptor superfamily (TNFRSF) members in the pathogenesis of inflammatory diseases. Exp. Mol. Med. 35: 8-16.
    OpenUrlCrossRefPubMed
  7. ↵
    Clarkson, M. R., M. H. Sayegh. 2005. T-cell costimulatory pathways in allograft rejection and tolerance. Transplantation 80: 555-563.
    OpenUrlCrossRefPubMed
  8. ↵
    Watts, T. H.. 2005. TNF/TNFR family members in costimulation of T cell responses. Annu. Rev. Immunol. 23: 23-68.
    OpenUrlCrossRefPubMed
  9. ↵
    van Assche, G., S. Vermeire, P. Rutgeerts. 2007. Emerging biological treatments in inflammatory bowel diseases. Minerva Gastroenterol. Dietol. 53: 249-255.
    OpenUrlPubMed
  10. ↵
    Barrie, A., S. Plevy. 2006. Treatment of immune-mediated extraintestinal manifestations of inflammatory bowel disease with infliximab. Gastroenterol. Clin. North Am. 35: 883-893.
    OpenUrlCrossRefPubMed
  11. ↵
    Borst, J., J. Hendriks, Y. Xiao. 2005. CD27 and CD70 in T cell and B cell activation. Curr. Opin. Immunol. 17: 275-281.
    OpenUrlCrossRefPubMed
  12. ↵
    Dolfi, D. V., P. D. Katsikis. 2007. CD28 and CD27 costimulation of CD8+ T cells: a story of survival. Adv. Exp. Med. Biol. 590: 149-170.
    OpenUrlCrossRefPubMed
  13. ↵
    Grewal, I. S.. 2008. CD70 as a therapeutic target in human malignancies. Expert Opin. Ther. Targets 12: 341-351.
    OpenUrlCrossRefPubMed
  14. ↵
    Tesselaar, K., Y. Xiao, R. Arens, G. M. van Schijndel, D. H. Schuurhuis, R. E. Mebius, J. Borst, R. A. van Lier. 2003. Expression of the murine CD27 ligand CD70 in vitro and in vivo. J. Immunol. 170: 33-40.
    OpenUrlAbstract/FREE Full Text
  15. ↵
    Iwamoto, S., M. Ishida, K. Takahashi, K. Takeda, A. Miyazaki. 2005. Lipopolysaccharide stimulation converts vigorously washed dendritic cells (DCs) to nonexhausted DCs expressing CD70 and evoking long-lasting type 1 T cell responses. J. Leukocyte Biol. 78: 383-392.
    OpenUrlAbstract/FREE Full Text
  16. ↵
    Sanchez, P. J., J. A. McWilliams, C. Haluszczak, H. Yagita, R. M. Kedl. 2007. Combined TLR/CD40 stimulation mediates potent cellular immunity by regulating dendritic cell expression of CD70 in vivo. J. Immunol. 178: 1564-1572.
    OpenUrlAbstract/FREE Full Text
  17. ↵
    Hendriks, J., L. A. Gravestein, K. Tesselaar, R. A. van Lier, T. N. Schumacher, J. Borst. 2000. CD27 is required for generation and long-term maintenance of T cell immunity. Nat. Immunol. 1: 433-440.
    OpenUrlCrossRefPubMed
  18. ↵
    Rowley, T. F., A. Al-Shamkhani. 2004. Stimulation by soluble CD70 promotes strong primary and secondary CD8+ cytotoxic T cell responses in vivo. J. Immunol. 172: 6039-6046.
    OpenUrlAbstract/FREE Full Text
  19. ↵
    Tesselaar, K., R. Arens, G. M. van Schijndel, P. A. Baars, M. A. van der Valk, J. Borst, M. H. van Oers, R. A. van Lier. 2003. Lethal T cell immunodeficiency induced by chronic costimulation via CD27-CD70 interactions. Nat. Immunol. 4: 49-54.
    OpenUrlCrossRefPubMed
  20. ↵
    Han, B. K., A. M. White, K. H. Dao, D. R. Karp, E. K. Wakelan, L. S. Davis. 2005. Increased prevalence of activated CD70+CD4+ T cells in the periphery of patients with systemic lupus erythematosus. Lupus 14: 598-606.
    OpenUrlAbstract/FREE Full Text
  21. ↵
    Lee, W. W., Z. Z. Yang, G. Li, C. M. Weyand, J. J. Goronzy. 2007. Unchecked CD70 expression on T cells lowers threshold for T cell activation in rheumatoid arthritis. J. Immunol. 179: 2609-2615.
    OpenUrlAbstract/FREE Full Text
  22. ↵
    Yamada, A., A. D. Salama, M. Sho, N. Najafian, T. Ito, J. P. Forman, R. Kewalramani, S. Sandner, H. Harada, M. R. Clarkson, et al 2005. CD70 signaling is critical for CD28-independent CD8+ T cell-mediated alloimmune responses in vivo. J. Immunol. 174: 1357-1364.
    OpenUrlAbstract/FREE Full Text
  23. ↵
    Nakajima, A., H. Oshima, C. Nohara, S. Morimoto, S. Yoshino, T. Kobata, H. Yagita, K. Okumura. 2000. Involvement of CD70-CD27 interactions in the induction of experimental autoimmune encephalomyelitis. J. Neuroimmunol. 109: 188-196.
    OpenUrlCrossRefPubMed
  24. ↵
    Laouar, A., V. Haridas, D. Vargas, X. Zhinan, D. Chaplin, R. A. Lier, N. van Manjunath. 2005. CD70+ antigen-presenting cells control the proliferation and differentiation of T cells in the intestinal mucosa. Nat. Immunol. :
  25. ↵
    Abadia-Molina, A. C., H. Ji, W. A. Faubion, A. Julien, Y. Latchman, H. Yagita, A. Sharpe, A. K. Bhan, C. Terhorst. 2006. CD48 controls T-cell and antigen-presenting cell functions in experimental colitis. Gastroenterology 130: 424-434.
    OpenUrlCrossRefPubMed
  26. ↵
    Neurath, M. F., I. Fuss, M. Pasparakis, L. Alexopoulou, S. Haralambous, K. H. Meyer zum Buschenfelde, W. Strober, G. Kollias. 1997. Predominant pathogenic role of tumor necrosis factor in experimental colitis in mice. Eur. J. Immunol. 27: 1743-1750.
    OpenUrlCrossRefPubMed
  27. ↵
    Uhlig, H. H., B. S. McKenzie, S. Hue, C. Thompson, B. Joyce-Shaikh, R. Stepankova, N. Robinson, S. Buonocore, H. Tlaskalova-Hogenova, D. J. Cua, F. Powrie. 2006. Differential activity of IL-12 and IL-23 in mucosal and systemic innate immune pathology. Immunity 25: 309-318.
    OpenUrlCrossRefPubMed
  28. ↵
    Powrie, F., M. W. Leach, S. Mauze, L. B. Caddle, R. L. Coffman. 1993. Phenotypically distinct subsets of CD4+ T cells induce or protect from chronic intestinal inflammation in C. B-17 scid mice. Int. Immunol. 5: 1461-1471.
    OpenUrlAbstract/FREE Full Text
  29. ↵
    Neurath, M., I. Fuss, W. Strober. 2000. TNBS-colitis. Int. Rev. Immunol. 19: 51-62.
    OpenUrlCrossRefPubMed
  30. ↵
    Xiao, Y., V. Peperzak, A. M. Keller, J. Borst. 2008. CD27 Instructs CD4+ T cells to provide help for the memory CD8+ T cell response after protein immunization. J. Immunol. 181: 1071-1082.
    OpenUrlAbstract/FREE Full Text
  31. ↵
    Hendriks, J., Y. Xiao, J. W. Rossen, K. F. van der Sluijs, K. Sugamura, N. Ishii, J. Borst. 2005. During viral infection of the respiratory tract, CD27, 4-1BB, and OX40 collectively determine formation of CD8+ memory T cells and their capacity for secondary expansion. J. Immunol. 175: 1665-1676.
    OpenUrlAbstract/FREE Full Text
  32. ↵
    Hendriks, J., Y. Xiao, J. Borst. 2003. CD27 promotes survival of activated T cells and complements CD28 in generation and establishment of the effector T cell pool. J. Exp. Med. 198: 1369-1380.
    OpenUrlAbstract/FREE Full Text
  33. ↵
    Soares, H., H. Waechter, N. Glaichenhaus, E. Mougneau, H. Yagita, O. Mizenina, D. Dudziak, M. C. Nussenzweig, R. M. Steinman. 2007. A subset of dendritic cells induces CD4+ T cells to produce IFN-γ by an IL-12-independent but CD70-dependent mechanism in vivo. J. Exp. Med. 204: 1095-1106.
    OpenUrlAbstract/FREE Full Text
  34. ↵
    Hayakawa, Y., M. J. Smyth. 2006. CD27 dissects mature NK cells into two subsets with distinct responsiveness and migratory capacity. J. Immunol. 176: 1517-1524.
    OpenUrlAbstract/FREE Full Text
  35. ↵
    Takeda, K., H. Oshima, Y. Hayakawa, H. Akiba, M. Atsuta, T. Kobata, K. Kobayashi, M. Ito, H. Yagita, K. Okumura. 2000. CD27-mediated activation of murine NK cells. J. Immunol. 164: 1741-1745.
    OpenUrlAbstract/FREE Full Text
  36. ↵
    Grundy, M. A., C. L. Sentman. 2006. Immunodeficient mice have elevated numbers of NK cells in non-lymphoid tissues. Exp. Cell. Res. 312: 3920-3926.
    OpenUrlCrossRefPubMed
  37. ↵
    Fort, M. M., M. W. Leach, D. M. Rennick. 1998. A role for NK cells as regulators of CD4+ T cells in a transfer model of colitis. J. Immunol. 161: 3256-3261.
    OpenUrlAbstract/FREE Full Text
  38. ↵
    Arens, R., K. Tesselaar, P. A. Baars, G. M. van Schijndel, J. Hendriks, S. T. Pals, P. Krimpenfort, J. Borst, M. H. van Oers, R. A. van Lier. 2001. Constitutive CD27/CD70 interaction induces expansion of effector-type T cells and results in IFNγ-mediated B cell depletion. Immunity 15: 801-812.
    OpenUrlCrossRefPubMed
  39. ↵
    McDonagh, C. F., K. M. Kim, E. Turcott, L. L. Brown, L. Westendorf, T. Feist, D. Sussman, I. Stone, M. Anderson, J. Miyamoto, et al 2008. Engineered anti-CD70 antibody-drug conjugate with increased therapeutic index. Mol. Cancer Ther. 7: 2913-2923.
    OpenUrlAbstract/FREE Full Text
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