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The Journal of Immunology, 2001, 167: 4796-4800.
Copyright © 2001 by The American Association of Immunologists

Cutting Edge

Cutting Edge: Membrane Lymphotoxin Regulates CD8+ T Cell-Mediated Intestinal Allograft Rejection1

Zhong Guo2,*, Jun Wang2,*, Lingzhong Meng{dagger}, Qiang Wu{ddagger}, Oliver Kim{ddagger}, John Hart{ddagger}, Gang He§, Ping Zhou§, J. Richard Thistlethwaite, Jr.{dagger}, Maria-Luisa Alegre§, Yang-Xin Fu3,{ddagger} and Kenneth A. Newell3,4,*

* Emory Transplant Center and Department of Surgery, Emory University School of Medicine, Atlanta, GA 30322; and the Departments of {dagger} Surgery, {ddagger} Pathology, and § Medicine, University of Chicago, Chicago, IL 60637


   Abstract
Top
 Abstract
Introduction
 Materials and Methods
 Results and Discussion
 References
 
Blocking the CD28/B7 and/or CD154/CD40 costimulatory pathways promotes long-term allograft survival in many transplant models where CD4+ T cells are necessary for rejection. When CD8+ T cells are sufficient to mediate rejection, these approaches fail, resulting in costimulation blockade-resistant rejection. To address this problem we examined the role of lymphotoxin-related molecules in CD8+ T cell-mediated rejection of murine intestinal allografts. Targeting membrane lymphotoxin by means of a fusion protein, mAb, or genetic mutation inhibited rejection of intestinal allografts by CD8+ T cells. This effect was associated with decreased monokine induced by IFN-{gamma} (Mig) and secondary lymphoid chemokine (SLC) gene expression within allografts and spleens respectively. Blocking membrane lymphotoxin did not inhibit rejection mediated by CD4+ T cells. Combining disruption of membrane lymphotoxin and treatment with CTLA4-Ig inhibited rejection in wild-type mice. These data demonstrate that membrane lymphotoxin is an important regulatory molecule for CD8+ T cells mediating rejection and suggest a strategy to avoid costimulation blockade-resistant rejection.


   Introduction
Top
 Abstract
 Introduction
Materials and Methods
 Results and Discussion
 References
 
In addition to the TCR, several molecules expressed by T cells function as important regulators of immune responses (1). A subset of these molecules, costimulatory molecules, are promising targets for manipulation in many disease states (2). In many experimental transplant models blockade of the CD28/B7 or CD154/CD40 costimulatory pathways has been shown to inhibit the rejection of allogeneic and xenogeneic grafts in rodents and primates (3, 4, 5, 6). Despite the frequent success of this strategy, it has been increasingly recognized that costimulatory blockade fails to prevent rejection in a number of transplant models. This phenomenon has been termed costimulation blockade-resistant rejection. Initial examples include the failure of CTLA4-Ig to inhibit the rejection of intestinal allografts and the inability of an anti-CD154 mAb to inhibit skin graft rejection (7, 8). The failure of CD28 and CD154 blockade to prolong allograft survival has been shown to correlate with resistance of CD8+ T cells to the blockade of these molecules (7, 8, 9, 10, 11). Thus, while costimulatory blockade effectively inhibits CD4+ T cell-mediated rejection, similar approaches to control CD8+ T cell-mediated rejection have not been described.

Lymphotoxin-related proteins, which belong to the TNF/TNFR superfamilies, are also important regulators of immune responses and as such are promising targets for modulating recipient responses to transplanted organs. Members of the lymphotoxin-related family of proteins expressed by T cells include herpes virus entry mediator (HVEM)5 and membrane lymphotoxin (mLT). HVEM binds a TNF-like molecule homologous to lymphotoxins, showing inducible expression, competing with HSV glycoprotein D for HVEM, a receptor expressed by T lymphocytes (LIGHT), which is expressed by immature dendritic cells (DC), resulting in enhanced T cell proliferation and cytokine production, suggesting that HVEM/LIGHT interactions provide a costimulatory signal for T cells (12). The binding of mlT expressed by T cells and activated B cells to lymphotoxin {beta} receptor (LT{beta}R) expressed on stromal cells and cells of monocytic origin has been shown to be critical for the development of lymphoid organs (13) and for the regulation of chemokine production (14). Disruption of these molecular interactions has been reported to impair the immune response to viruses and tumors (15, 16, 17, 18, 19).

The purpose of the current study was to determine whether manipulation of these lymphotoxin-related molecules could be used to inhibit costimulation blockade-resistant, CD8+ T cell-mediated allograft rejection. To test this hypothesis we used a heterotopic murine intestinal transplant model. This model offers the advantage that, unlike the murine cardiac transplant model, either CD4+ or CD8+ T cells can mediate rejection (20). However, because this model lacks physical characteristics amenable to serial, noninvasive monitoring, and because recipient survival is not dependent upon the survival of the heterotopic graft, the assessment of transplanted intestines was based upon their histologic appearance.


   Materials and Methods
Top
 Abstract
 Introduction
 Materials and Methods
Results and Discussion
 References
 
Mice

C57BL/6 (H-2b), C57BL/6 x C3H/HeJ (B6C3F1/J, H-2bxk), and C57BL/6-Cd4tmlMak (CD4-/-, H-2b) mice were purchased from The Jackson Laboratory (Bar Harbor, ME) and the National Cancer Institute (Frederick, MD). LT{alpha}-/- mice, back-crossed six generations onto the C57BL/6 background, have been previously described (21).

Intestinal transplantation and histologic graft assessment

Intestinal transplantation was performed as described (20). Intestine grafts were revascularized by anastomosing the portal vein to the recipient inferior vena cava and the superior mesenteric artery to the recipient infrarenal aorta. The jejunum was exteriorized as a stoma and the ileum was anastomosed to the side of the recipient jejunum. Specimens for histologic assessment were fixed in 10% buffered formalin and embedded in paraffin. H&E-stained 3-µm sections were evaluated by a pathologist in a "blinded" fashion. Rejection was graded according to the following definitions: 0, no rejection; 1, scattered apoptotic crypt cells; 2, focal crypt destruction; and 3, mucosal ulceration with or without transmural necrosis.

Study design

To avoid graft-vs-host disease (GVHD), a F1 into parent transplant model was used. Allografts were procured from B6C3F1/J mice (H-2bxk). The genetic background of all recipient mice was C57BL/6J (H-2b). Technical failures, defined as mice that died within the first 3 days, were excluded from analysis.

Fusion proteins and mAb

LT{beta}R-Ig is comprised of the LT{beta}R extracellular domain attached to the CH2 and CH3 domains of human IgG1 (13). Recipient mice were treated with 100 µg administered i.p. on days 0 and 7. Mice in control groups were treated with human IgG. The fusion protein mCTLA4-Ig was provided by M. Collins (Genetics Institute, Cambridge, MA). Recipient mice were treated with 50 µg of mCTLA4-Ig administered i.p. every other day for 14 days beginning on the day of transplantation. BBF6-BF2, a mAb that is specific for the {beta}-chain of mlT, was provided by J. Browning (Biogen, Cambridge, MA). This mAb was administered i.p. at a dose of 100 µg on days 0, 3, and 7.

RT-PCR

Total RNA was isolated from intestinal grafts frozen by liquid nitrogen using a RNeasy Mini Kit (Qiagen, Hilden, Germany). Samples were treated with RNase-free DNase (Amersham Pharmacia Biotech, Piscataway, NJ). Total RNA (3–5 µg) was reverse transcribed using the First Strand cDNA Synthesis kit (Amersham Pharmacia Biotech). The mRNA encoding GAPDH, Mig, and SLC were detected by real-time RT-PCR using the ABI Prism 7700-sequence detection system (Applied Biosystems, Foster City, CA) as described (11). The primer and probe sequences were designed using the software program Primer Express Version 1.0 (Applied Biosystems). Sequences used to detect GAPDH, Mig, and SLC are as follows: GAPDH forward primer, 5'-TTCACCACCATGGAGAAGGC-3'; reverse primer, 5'-GGCATGGACTGTGGTCATGA-3'; probe, 5'-TGCATCCTGCACCACCAACTGCTTAG-3'; Mig forward primer, 5'-GCCATGAAGTCCGCTGTTCT-3'; reverse primer, 5'-GGTTCCTCGAACTCCACACTG-3'; probe, 5'-TTCCTTTTGGGCATCATCTTCCTGGA-3'; SLC forward primer, 5'-AGACTCAGGAGCCCAAAGCA-3'; reverse primer, 5'-GTTGAAGCAGGGCAAGGG T-3'; and probe, 5'-CCACCTCATGCTGGCCTCCGTC-3'.

Reactions were performed using 20-µl reaction volumes and the TaqMan Universal PCR master mixture (Applied Biosystems). PCR conditions: 50°C for 2 min, 95°C for 10 min. Each amplification was 15 s at 95°C and 1 min at 60°C for 40 cycles. PCR results were analyzed using the relative standard curve method.

Statistical analysis

Rejection grades were compared using the Kruskal-Wallis test for samples from multiple groups and the Mann-Whitney U test for samples from two groups. Continuous variables were compared using the unpaired t test with Welch correction. Calculations were performed using InStat version 2 (GraphPad, San Diego, CA). Values of p < 0.05 were considered significant.


   Results and Discussion
Top
 Abstract
 Introduction
 Materials and Methods
 Results and Discussion
References
 
As an initial approach toward determining the role of lymphotoxin-related molecules in allograft rejection, intestinal allografts were transplanted into LT{alpha}-/- recipients. Although there was a trend toward a decrease in the severity of rejection in LT{alpha}-/- recipients (p = 0.07 vs wild-type controls), all recipients did develop rejection (Fig. 1Go). Recent reports describing an association between disruption of mlT and defects in host immunity have linked this effect to impaired function of CD8+ T cells (15, 17). Thus, we hypothesized that the rejection observed in LT{alpha}-/- mice was mediated by CD4+ T cells. We have previously shown that CD4+ T cell-mediated rejection can be blocked by CTLA4-Ig (7). Therefore, to test the hypothesis, LT{alpha}-/- recipient mice were treated with CTLA4-Ig. Rejection was completely inhibited when LT{alpha}-/- mice were treated with CTLA4-Ig, whereas CTLA4-Ig had no effect on rejection in wild-type recipients (Fig. 1Go). These data suggest that LT{alpha}-related molecules contribute significantly to the process of allograft rejection and that this effect is predominantly on CD8+ T cells. Several mechanisms could explain this effect. Secreted lymphotoxin LT{alpha}3, which is absent in LT{alpha}-/- mice, may contribute to intestinal allograft rejection. Similarly, mlT, which is comprised of LT{alpha} and LT{beta}, is also absent in LT{alpha}-/- mice and may play a role in allograft rejection. Alternatively, the disruption of splenic architecture and the paucity of lymph nodes associated with the LT{alpha}-/- phenotype (22) may be responsible for the impaired immune response to intestinal allografts. This is consistent with the observation that splenectomized aly/aly mutant mice, which lack lymph nodes and splenic tissue, fail to reject heart allografts (23).



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  		FIGURE 1. CTLA4-Ig inhibits intestinal allograft rejection in LT{alpha}-/- recipients. Recipient mice were treated as described with CTLA4-Ig. On day 14 following transplantation, grafts were assessed histologically. Day 14 syngeneic grafts showed no evidence of rejection (rejection score, all grafts, 0). Each {diamondsuit} represents the score for an individual recipient. The heavy lines (—) represent the mean score for the indicated group.

 
To distinguish between these possibilities, we treated CD4-/- intestinal allograft recipients with LT{beta}R-Ig that binds mlT and LIGHT but not LT{alpha}3. We have previously shown that in CD4-/- mice rejection is dependent upon CD8+ T cells (20). Treatment with LT{beta}R-Ig significantly inhibited CD8+ T cell-mediated rejection at day 14 (Fig. 2Go, p < 0.01). This protective effect persisted at day 28, although three of the four treated mice had developed moderate rejection (mean rejection grade (MRG) 1.5 ± 1.0, n = 4, p = 0.04 vs day 14 CD4-/- control group). These data demonstrate a role for either mlT or LIGHT in the process of intestinal allograft rejection and imply that the defect in CD8+ T cell-mediated rejection in LT{alpha}-/- mice is at least in part due to the disruption of mlT. The failure of LT{beta}R-Ig to promote long-term allograft survival in this model could be due to incomplete blockade of mlT and LIGHT or the ability of other effector mechanisms to mediate rejection independent of mlT and LIGHT.



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  		FIGURE 2. Either LT{beta}R-Ig or an anti-LT{beta} mAb inhibits the rejection of intestinal allografts in CD4-/- mice. Recipients were treated as described with either LT{beta}R-Ig, human IgG, or the anti-LT{beta} mAb BBF6-BF2. On day 14 following transplantation grafts were evaluated histologically. Each {diamondsuit} represents the score for an individual recipient. The heavy lines (—) represent the mean score for the indicated group.

 
Unlike the results obtained using LT{alpha}-/- mice, the results obtained using LT{beta}R-Ig cannot be attributed to an alteration in the structure of secondary lymphoid organs or loss of expression of LT{alpha}3. However, in addition to binding mlT, LT{beta}R-Ig also binds to LIGHT (24). The interaction of LIGHT with HVEM has been shown to deliver a signal that costimulates T cells (12, 19). Inhibition of the HVEM/LIGHT interaction by LT{beta}R-Ig has been reported to inhibit tumor growth, prevent the development of GVHD, and impair the development of alloreactive CTL (18, 19). Thus, the inhibition of allograft rejection associated with LT{beta}R-Ig could either be a consequence of its ability to bind mlT or its ability to bind LIGHT, thereby blocking the HVEM/LIGHT costimulatory pathway.

To distinguish between the effects of blocking mlT and LIGHT on the rejection of intestinal allografts by CD8+ T cells, we treated CD4-/- recipient mice with BBF6-BF2, a mAb specific for the {beta}-chain of the mlT complex. Blockade of mlT using this anti-LT{beta} mAb significantly inhibited the rejection of intestinal allografts by CD4-/- mice (Fig. 2Go, p < 0.01). These data confirm those obtained using LT{beta}R-Ig and directly demonstrate that mlT contributes to CD8+ T cell-mediated allograft rejection. Interestingly, the anti-LT{beta} mAb had little effect on intestinal allograft rejection mediated by CD4+ T cells in CD8-/- recipients (MRG 2.0 ± 0, n = 3). These data describe an important new role for mlT in allograft rejection and identify a novel strategy to inhibit costimulation blockade-resistant rejection. However, it should be noted that these data do not exclude a potential contribution of LIGHT to this process.

Mechanisms by which biological agents inhibit rejection can be grouped into those that deplete alloreactive T cells, those that prevent complete T cell activation and induce anergy by blocking costimulatory signals, those that alter T cell differentiation, those that impair T cell migration, and those that induce the development of regulatory cells. Of these possible mechanisms, the engagement of HVEM by LIGHT costimulates T cells (12) and the engagement of mlT by LT{beta}R augments chemokine production (14), which in turn regulates cell migration. We postulated that one or both of these mechanisms contributed to the protective effect of disrupting lymphotoxin-related molecules on intestinal allograft rejection and undertook studies to test this hypothesis. Characteristically, agents that block T cell costimulatory molecules prevent complete T cell activation and consequently inhibit Ag-driven T cell proliferation. Unlike CLTA4-Ig, LT{beta}R-Ig did not inhibit the proliferation of naive T cells to alloantigens in vitro over a broad range of concentrations nor did it inhibit the proliferation of CD4+ or CD8+ T cells in vivo in a GVHD model (data not shown). These data suggest that LT{beta}R-Ig may inhibit rejection by mechanisms other than the prevention of T cell costimulation and activation.

Not having observed an effect of LT{beta}R-Ig on T cell costimulation, its effect on chemokine production was examined. Given the demonstrated role of Mig in allograft rejection (25), the effect of LT{beta}R-Ig and the anti-LT{beta} mAb on Mig gene expression was determined. Treatment of either wild-type or CD4-/- recipient mice with LT{beta}R-Ig significantly reduced Mig gene expression within intestinal allografts (Fig. 3Go, A and B). The anti-LT{beta} mAb also significantly reduced Mig gene expression in CD4-/- recipients (Fig. 3GoB). These data, together with the knowledge that migration of immune cells is regulated by concentration gradients of chemoattractant molecules such as Mig, suggest that LT{beta}R-Ig and anti-LT{beta} mAb-induced alterations in chemokine production within intestinal allografts may inhibit rejection by impairing the migration of leukocytes to the allograft. Although our data do not directly test this hypothesis, the importance of this potential mechanism warrants future investigation.



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  		FIGURE 3. Blockade of the mlT pathway inhibits Mig gene expression in intestinal allografts from wild-type (A) and CD4-/- (B) recipients. mRNA was isolated from intestinal allografts of recipient mice treated with LT{beta}R-Ig or the anti-LT{beta} mAb BBF6-BF2. Each {diamondsuit} represents the value corresponding to a single sample. The heavy lines (—) denote the mean value. Data are shown as the fold change in the ratio of transcripts encoding Mig and GAPDH in the indicated experimental group relative to the syngeneic group.

 
In addition to affecting the production of Mig, which regulates the migration of immune cells to sites of inflammation in peripheral tissues, mlT has been reported to affect the production of "lymphoid chemokines" such as SLC (14). The engagement of CCR7 by SLC has been reported to play an important role in bringing DC and T cells together in secondary lymphoid organs (26). Treatment with LT{beta}R-Ig or an anti-LT{beta} mAb dramatically reduced SLC gene expression within the spleens of CD4-/- or wild-type intestinal allograft recipients (Fig. 4Go). Consistent with this result and the known effects of SLC, we observed a substantial reduction in the number of DC in the spleens of CD4-/- recipient mice treated with anti-LT{beta} mAb as compared with CD4-/- recipients treated with a control mAb (data not shown). This is also compatible with our previous data that demonstrated a decrease in the number of splenic DC in wild-type, untransplanted mice treated with LT{beta}R-Ig (13, 22). It has previously been demonstrated that following abdominal transplantation of allogeneic hearts DC migrate to the spleen (27) and that the spleen is an important site for T cell priming (23). In light of these observations, our data suggest that disrupting mlT inhibits chemokine production within the spleen, thereby impairing DC migration and T cell priming.



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  		FIGURE 4. Treatment with LT{beta}R-Ig or an anti-LT{beta} mAb is associated with decreased SLC gene expression in the spleens of wild-type and CD4-/- mice bearing intestinal allografts. mRNA was isolated from the spleens of recipient mice treated with LT{beta}R-Ig or the anti-LT{beta} mAb BBF6-BF2. Each {diamondsuit} represents the value corresponding to a single sample. The heavy lines (—) denote the mean value. Data are displayed as the fold change in the ratio of SLC:GAPDH for the experimental groups relative to the syngeneic group.

 
To evaluate the potential of these reagents in a therapeutically more relevant model, wild-type mice were used as recipients. Treatment with LT{beta}R-Ig failed to inhibit rejection of intestinal allografts in wild-type mice (MRG 2.4 ± 0.5, n = 5 vs 2.4 ± 1.0 for wild-type control mice, n = 10). Given our previous observation that blocking mlT had little effect on CD4+ T cell-mediated rejection, we treated wild-type recipients with a combination of CTLA4-Ig to inhibit CD4+ T cell-mediated rejection and LT{beta}R-Ig to inhibit CD8+ T cell-mediated rejection. Combined treatment significantly inhibited intestinal allograft rejection in wild-type recipients (MRG 1.1 ± 1.1, n = 10 vs CTLA4-Ig MRG 2.6 ± 0.7, n = 8 or LT{beta}R-Ig MRG 2.4 ± 0.5, n = 5; p = 0.01 and 0.04 respectively). In models where rejection is more dependent upon CD4+ T cells, short courses of treatment with some agents have been shown to promote long-term allograft acceptance through the induction of regulatory T cells (9). Our data demonstrate that controlling both CD4+ and CD8+ T cells significantly inhibited rejection in the intestinal transplant model and suggest that this approach may be useful clinically. However, although significantly less severe, the observation that seven of the 10 recipients did develop rejection suggests that this strategy may not promote tolerance.

In summary, these data provide the first demonstration that mlT regulates the recipient immune response to transplanted organs. Equally important, blockade of this pathway inhibits CD8+ T cell-mediated allograft rejection, suggesting an approach to costimulation blockade-resistant rejection. Our data, together with published data, suggest that treatment-induced alterations in chemokine production may contribute to this effect, perhaps by impairing the migration of T cells and DC to the allograft and spleen. Lastly, these data demonstrate that combinations of agents that bind mlT and costimulatory molecules may represent a clinically applicable immunosuppressive strategy when both CD4+ and CD8+ T cells contribute to allograft rejection.


   Acknowledgments
 
We thank Drs. Jeffrey Browning, Christian P. Larsen, and Thomas C. Pearson for critical review of the manuscript.


   Footnotes
 
1 This work was supported by Grants RO1 AI43579 (to K.A.N.) and R01 HD73104 (to Y.-X.F.) from the National Institutes of Health and Grant JDFI 1-2000-875 (to Y.-X.F.) from the Juvenile Diabetes Foundation. Back

2 X.G. and J.W. contributed equally to this work. Back

3 Y.-X.F. and K.A.N. should be considered co-senior authors. Back

4 Address correspondence and reprint requests to Dr. Kenneth A. Newell, Department of Surgery, Emory University, WMB 5105, 1639 Pierce Drive, Atlanta, GA 30322. E-mail address: kenneth.newell{at}emory.org Back

5 Abbreviations used in this paper: HVEM, herpes virus entry mediator; LT{beta}R, lymphotoxin {beta} receptor; mLT, membrane lymphotoxin; LIGHT, a TNF-like molecule homologous to lymphotoxins, showing inducible expression, competing with HSV glycoprotein D for HVEM, a receptor expressed by T lymphocytes; DC, dendritic cell; SLC, secondary lymphoid chemokine; MRG, mean rejection grade; Mig, monokine induced by IFN-{gamma}; GVHD, graft-vs-host disease. Back

Received for publication July 31, 2001. Accepted for publication September 10, 2001.


   References
Top
 Abstract
 Introduction
 Materials and Methods
 Results and Discussion
 References
 

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