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Conceived and designed the experiments: WWJU DLG BOR. Performed the experiments: WWJU TP JRFA SL SMvdK ARvdS. Analyzed the data: WWJU TP SL SMvdK. Contributed reagents/materials/analysis tools: MGDK MG JWD DVS LDS. Wrote the paper: WWJU TP DLG BOR.
Despite increasing evidence that autoreactive CD8 T-cells are involved in both the initiation of type 1 diabetes (T1D) and the destruction of beta-cells, direct evidence for their destructive role in-vivo is lacking. To address a destructive role for autoreactive CD8 T-cells in human disease, we assessed the pathogenicity of a CD8 T-cell clone derived from a T1D donor and specific for an HLA-A2-restricted epitope of islet-specific glucose-6-phosphatase catalytic-subunit related protein (IGRP). HLA-A2/IGRP tetramer staining revealed a higher frequency of IGRP-specific CD8 T-cells in the peripheral blood of recent onset human individuals than of healthy donors. IGRP265–273-specific CD8 T-cells that were cloned from the peripheral blood of a recent onset T1D individual were shown to secrete IFNγ and Granzyme B after antigen-specific activation and lyse HLA-A2-expressing murine islets in-vitro. Lytic capacity was also demonstrated in-vivo by specific killing of peptide-pulsed target cells. Using the HLA-A2 NOD-scid IL2rγnull mouse model, HLA-A2-restricted IGRP-specific CD8 T-cells induced a destructive insulitis. Together, this is the first evidence that human HLA-restricted autoreactive CD8 T-cells target HLA-expressing beta-cells in-vivo, demonstrating the translational value of humanized mice to study mechanisms of disease and therapeutic intervention strategies.
Non-obese diabetic (NOD) mice are widely used for studying the pathogenesis and therapy of autoimmune type 1 diabetes (T1D) . Autoreactive CD4 and CD8 T-cells in NOD mice infiltrate and subsequently destroy the insulin-producing beta-cells in pancreatic islets, resulting in dysregulation of blood glucose levels and hyperglycemia ; . Although studies using NOD mice have helped to define mechanisms of disease pathogenesis and to identify potential interventional and therapeutic strategies in autoimmune diabetes, there are discrepancies between disease pathogenesis in NOD mice and in humans. For example, while the lymphocytic infiltrate in the NOD pancreas is extensive, insulitis in humans is multi-focal and targets islets scattered throughout a pancreas ; .
The recruitment of autoreactive CD4 T-cells is required for the initiation of autoreactivity in NOD mice, yet CD8 T-cells are increasingly being recognized as key pathogenic mediators in the destruction of beta-cells and progression of the disease in both diabetic NOD mice and humans –. Deficiency of CD8 T-cells due to the absence of MHC class I in NOD mice renders these mice completely resistant to T1D ; . In humans, susceptibility to T1D is strongly associated with the HLA-A2 haplotype, with 60–70% of affected individuals expressing this allele . Transgenic expression of HLA-A2 significantly accelerates disease onset in NOD mice, and is associated with the early appearance of HLA-A2-restricted CD8+ T-cells in prediabetic insulitic lesions .
The epitopes recognized by autoreactive cytotoxic T-cells are thought to be primarily derived from beta-cell proteins, and the identity of these epitopes in humans remains under active investigation. A known target of autoreactive CD8 T-cells in the NOD mouse is islet-specific glucose-6-phosphatase catalytic-subunit related protein (IGRP) ; . Several epitopes from IGRP have been identified using HLA-A2 transgenic (Tg) NOD mice , and some of these epitopes are also targeted by CD8 T-cells in T1D individuals ; . In addition, the IGRP-specific CD8 T-cells from HLA-A2 Tg NOD mice lyse human HLA-A2+ beta-cells in-vitro, demonstrating the potential utility of HLA-A2 Tg NOD mice for identifying HLA-restricted islet autoantigens and for investigating the pathogenesis of human T1D .
To date, however, direct evidence that human diabetogenic CD8 T-cells target beta-cells in-vivo is lacking. The diabetogenic role of CD8 T-cells was suggested by correlation between increased frequencies of islet autoreactive CD8 T-cells in T1D islet allograft recipients that exhibited recurrent islet autoimmunity and loss of graft beta-cell function . Furthermore, islet-autoreactive CD8 T-cells from individuals reactive with preproinsulin selectively killed human islet cells in-vitro in a glucose concentration-dependent fashion, suggesting cross-talk between the immune system and pancreatic beta-cells . Very recently, we could demonstrate the presence of IGRP-specific CD8 T cells in insulitis lesions of human T1D patients, which is strong indication for their role in the beta-cell destruction process in humans . To close the critical gap in knowledge of disease mechanisms in T1D in humans, novel preclinical models are needed to investigate the pathogenicity of human autoreactive T-cells in-vivo. Recently, NOD-scid IL2rγnull mice have been developed – that readily engraft with human PBL  and are transgenic for HLA-A2 ; .
We and others have shown that human HLA-A2-restricted CD8 T-cells can recognize the IGRP265–273 epitope conserved between mice and humans ; . To test the involvement of CD8 T-cells specific for this epitope in beta-cell destruction, we cloned these cells from the peripheral blood of a recent onset T1D individual. We then used the new generation of HLA-A2 Tg immunodeficient humanized mice to assess the pathogenicity of human effector immune cells in-vitro and in-vivo .
IGRP265–273 has been identified as an epitope of islet autoreactive CD8 T cells using NOD-β2mtm1Unc HHD Tg mice that express a chimeric HLA-A2.1/H-2Db molecule . To assess potential involvement of CD8 T-cells specific for this epitope in islet-cell destruction in-vivo, IGRP265–273 cells were cloned from the peripheral blood of a recent onset T1D individual. Selective binding of this epitope to HLA-A2 was determined (Figure S1). Using A2/IGRP tetramers and CD8 antibodies, IGRP-specific CD8 T-cells were identified in PBMC of HLA-A2+ recent onset individuals but not of healthy controls, confirming previous findings (Figure 1A). Double positive cells were sorted at one cell per well and stimulated using peptide-pulsed APC and feeders. Three weeks later, IGRP-specific CD8 T-cell clones were identified that stained with HLA-A2-specific tetramer but not with an HLA-A2-control tetramer (Figure 1B).
From the available clones, we selected one for further characterization. Analysis of clone 7 TCR-Vα and -Vβ transcripts using specific primers revealed message for Vα19 and Vβ13 only, which, in combination with VDR3 length variation analysis, confirmed clonality of this T-cell population (Table S1). Clone 7 T-cells (hereafter referred to as IGRP-specific T-cells) expressed markers necessary for strong antigen recognition (CD2 and CD28), as well as the activation- and memory markers HLA-DR and CD45RO (Figure S2). Activation of the IGRP265–273-specific T-cells with their cognate antigen resulted in secretion of IFNγ but not IL-10 (Figure 1C). No cytokine production was detected when APC were loaded with a control HLA-A2 binding peptide, demonstrating the antigen specificity of these T-cells (Figure 1C). In addition, IGRP-specific T-cells produced IL-2 and TNFα upon antigen-specific activation, but not IL-4 (data not shown), endorsing these cells with an overt effector phenotype . Furthermore, antigen-specific activation of these CD8 T-cells led to cytotoxic activity as shown by expression of CD107a, which is present in the membrane of cytotoxic granules, production of GrB as well as lysis of peptide-pulsed HLA-A2+ target-cells (Figure 1C,D and and2A).2A). The efficacy of the IGRP-specific T-cell clone to recognize the IGRP265–273 epitope was demonstrated in peptide-dose titration cytotoxicity assays, indicating that the IGRP-specific T-cell clone had a relatively low avidity for its ligand, since 1 µM peptide was required to attain 50% of the maximal response (Figure 2B). A hallmark of low-avidity T-cells is CD8-dependent binding of peptide/MHC complexes ; . Anti-CD8 antibody completely blocked tetramer labeling (Figure 2C). Furthermore, T-cells stained negative with IGRP265–273 tetramers of HLA-A2 molecules mutated in their CD8-binding α3 region ; .
We next examined the potential of the IGRP-specific T-cell clone to recognize naturally processed and presented IGRP epitope by testing its reactivity with HLA-A2 expressing murine islets. Since dissociated islet-cells exhibit a high degree of spontaneous death that can complicate data interpretation, we used a previously described assay in which intact islets are allowed to adhere and form monolayers before use . We observed highly efficient islet cell killing of NOD-scid HHD Tg islets, even at very low effector:target (E:T) ratiós (Table 1), approximately 15% of the NOD-scid. HHD Tg islet cells were lysed at an E:T ratio of 30, whereas only 0.6% HLA-A2-negative islets were killed (P<0.01). Lysis of NOD-scid HHD islets by IGRP-specific CD8 T-cells was significantly greater than with HLA-A2-restricted tumor-antigen-specific CD8 T-cells (Table 1).
To determine the cytotoxic activity of IGRP-specific CD8 T-cells in-vivo, we adapted a murine in-vivo cytotoxicity assay that is widely used to demonstrate cytotoxic actions of primed effector/memory CD8 T-cells ; . HLA-A2+ target cells (PBMC) were labeled with different concentrations of CFSE, pulsed with either IGRP265–273 or irrelevant peptide, mixed and injected into NOD-scid IL2rγnull mice that had received an intrasplenic injection of IGRP-specific T-cells 24 h earlier. Mice that had not been injected with the human T-cell clone were used as a negative control. IGRP-specific T-cells lysed IGRP-pulsed target cells in-vivo, as demonstrated by the specific disappearance of the CFSEhi-labeled target cells pulsed with IGRP-peptide (Table 2). In contrast, the number of CFSElo-labeled targets pulsed with control peptide remained unchanged, even in the presence of the IGRP-specific T-cells.
We next investigated whether human IGRP-specific CD8 T-cells can target and destroy HLA-A2 pancreatic beta-cells in-vivo. The expression of both CD62L and the chemokine receptors CXCR3 and CCR4 (Figure S2) indicates that the IGRP-specific T-cells express adhesion markers required to migrate to secondary lymphoid tissue and inflamed pancreatic tissue ; . Since NOD-scid IL2rγnull HHD mice are devoid of cytokines necessary for homeostatic T-cell proliferation, we hypothesized that the survival of the human CD8 T-cell clone would be facilitated by injecting human PBMC from non-diabetic donors 48 h earlier. This time span would be sufficient for the PBMC to expand in the lymphopenic environment and produce the necessary cytokines that may be required for survival of cloned CD8 T-cell in the absence of CD4 T-cell help. As a control, a diabetes-unrelated CD8 T-cell clone was injected intrapancreatically. Additional control mice received a sham-injection.
No changes in blood glucose levels were detected following injection of either IGRP-specific or control T-cell clones (data not shown). Four weeks after adoptive transfer of the human T-cell clones the pancreas was recovered and analyzed by histology for islet integrity and presence of the IGRP-specific CD8 T-cells. Both human IGRP-specific and control CD8 T-cells were present at detectable levels four weeks after injection (Figure 3A). However, their location differed greatly. Pancreata of recipient mice of IGRP-specific T-cells predominantly elicited intra-islet infiltration (Figure 3A). In contrast, control CD8 T-cells remained at the perivascular sites. Mice receiving a sham injection showed no infiltration of islets. Notably, insulin staining of pancreatic sections revealed that the islets were disrupted only in mice injected with the IGRP-specific T-clone, but not in those receiving the control CD8 T-cells or a sham injection (Figure 3A). The number of islets infiltrated with T-cells was significantly greater in mice injected with the IGRP T-clone, 10/49 (20%) than mice injected with the control T-clone, where none of 20 investigated islets showed infiltrating cells, although T-cells were occasionally found around the islets. (p=0.013; two-tailed Fisher exact test). Moreover, absence of insulin staining was accompanied by positivity for cCaspase-3, pointing to beta-cell destruction by IGRP-specific T-cells (Figure 3B). Pancreata of mice that received control CD8 T-cells were negative for cCaspase-3 staining.
This study provides the first evidence that autoreactive CD8 T-cells cloned from a T1D individual can participate in islet cell destruction in-vivo using a novel humanized mouse model. IGRP265–273-specific CD8 T-cells producing IFNγ and expressing CD107a upon antigen-specific activation are capable of lysing murine HLA-A2 expressing islets in-vitro. In-vivo, these T-cells lysed target cells pulsed with islet peptide. Following intra-pancreatic injection into HLA-A2 transgenic NOD-scid IL2rγnull HHD mice, IGRP-specific CTLs localized to the islets and caused beta-cell destruction. However, no changes in blood glucose-levels were observed. No islet cell destruction was detected when mice were injected with equal numbers of control HLA-A2-restricted cloned CD8 T-cells.
The assumption that IGRP-specific CD8 T-cells possess diabetogenic potential in-vivo was based on the observation that these cloned T-cells were highly cytotoxic for HLA-A2 expressing islets in-vitro. However, the extent of lysis observed was low in comparison to lysis of peptide-pulsed EBV-LCL. This difference might be explained by lower expression of HLA-A2 molecule (HHD) on murine islets compared with HLA-A2 levels on human cells, which consequently results in decreased presentation of the IGRP epitope. In addition, the IGRP-specific T-cells possess low-avidity T-cell receptors as revealed by low staining with specific tetramer and CD8 dependency of tetramer staining. This may be inherent to autoreactive T-cells, since these should have been eliminated during thymic education due to high-avidity interactions with their cognate self-antigen. Thus, besides weak recognition of the epitope by the low-avidity TCR of the IGRP-specific T-cells, these observations are also consistent with low amount of IGRP epitope presentation on the surface of the islets.
Using an adapted in-vivo cytotoxicity assay, we obtained evidence that IGRP T-cells are capable of lysing targets in-vivo. Mobilization of effector CD8 T-cells to infected tissue requires CD4 T-help , however, CD4 T-cells only provide this help when specifically activated by their cognate antigen at this site . Given that human IGRP-specific CD4 T-cells were not available, we opted to inject the IGRP-specific CD8 T-cells intra-pancreatically and to provide the optimal cytokine milieu for survival of the transferred T-cells by systemic injection of HLA-A2+ PBMC from non-diabetic donors prior,for generation of the necessary cytokines (i.e. IL2, IL7, IL15) needed for T-cell homeostasis.
Immunohistochemical analysis of the pancreata four weeks after injection of the human CD8 T-cells revealed clear differences in localization between the IGRP-specific T-cells and control T-cells. IGRP-specific CTLs infiltrated into the islets, whereas control T-cells were retained in the peri-vascular areas. Our observation confirms previous findings that islet antigen expression is a key factor in governing the ability of the autoantigen-specific T-cells to accumulate in the islets ; ; . Interestingly, both CD4 and CD8 T-cells migrating into pancreatic tissue expressed the chemokine receptor CXCR3, while distressed beta-cells produce its ligand CXCL-10 (IP-10) . This feature may present a master switch for migration of islet autoreactive T-cells to the beta-cell environment, as suggested by preclinical studies . Some human leukocytes were noted in the exocrine pancreatic tissue in both mice injected with IGRP-specific T-cells and control T-cells, which may be partly due to their intrapancreatic injection causing tissue damage and chemokine production leading to inflammatory infiltrates. The CD45 staining will target the injected T-clones as well as co-injected PBMC. Yet, since the same PBMC donor was used for all three T cells clones, the insulitis lesions could be attributed to the particular humans T-cell clones injected, rather than the PBMC that were not as feeders of the CD8 T cells.
Injection of the IGRP-specific T-cells resulted in a destructive inflammation, but not when a high number of cells from a control HLA-A2-restricted CD8 T-cell clone were injected. Since no changes in blood glucose-levels of the recipient mice were observed upon injection of the IGRP-specific T-cells in spite of clear islet cell destruction, we speculate that adoptive transfer of islet-specific CD4 T-cells may be required for propagation and sustained CD8 T-cell expansion and cytotoxic activity . A recent study employing the same HLA-A2 NOD-scidIL2rγnull mouse model showed that high frequencies of CD4 T-cells were present when mice were engrafted with PBMC from a T1D patient . This was paralleled by the presence of diabetogenic epitope-specific CD8 T-cells. However, in this study no islet cell destruction was demonstrated, which may be due to lower frequency of islet-specific T-cells in the pancreas compared to our study. Yet, the fact that IGRP265–273-reactive CD8 T-cells were present among the islet-specific CD8 T-cells, as well as the recent finding that specific targeting of IGRP-reactive CD8 T-cells effectively inhibited diabetes development in NOD.β2mnull.HHD mice  corroborate our current findings that this epitope is pathogenic in human disease.
T-cell autoreactivity may require more than 4 weeks for complete beta cell destruction, and require CD4 T-cells acting in concert. Indeed, the limited survival of CD8 T-cell clones in mice in the absence of CD4 T-cells underscores this notion. Mouse CD4 T-cells specific for a low-affinity insulin-derived peptide required 20 weeks before hyperglycemia developed in 50% of recipient mice . Despite the great value of immunocompetent NOD mice, there are discrepancies between the etiopathogenesis of T1D in NOD mice versus humans. These differences include the pattern of insulitis. The intra-islet infiltration pattern of human islet-specific T-cells and islet destruction observed in our study closely resembles the pathogenesis found in human inflamed pancreas ;  rather than inflammatory lesion typically observed in NOD mice ; . The relevance of islet autoreactive T-cells circulating in the blood in the pathogenesis of insulitis in humans remains unresolved. Nonetheless, our current study on human peripheral blood CD8 T-cell clones, as well as our earlier studies on homing of human anti-islet CD4 T-cells clones to pancreatic tissue, imply that circulating human T-cells can contribute to insulitis. Recent studies on islet autoreactivity in an explanted human pancreas graft indicated that circulating islet-antigen autoreactive CD8 T-cells in peripheral blood were also present in pancreatic inflammatory lesions, albeit at a lower frequency. Moreover, additional islet autoreactivities that were below detection levels in the circulation could be detected in the inflamed pancreas .
In conclusion, our data provide first evidence that human autoreactive CD8 T-cells have the potential to target HLA-A2-matched beta-cells in-vivo, demonstrating the translational value of humanized mice to study mechanisms of disease and interventional strategies.
NOD.Cg-Prkdcscid Il2rgtm1Wjl/Sz (abbreviated as NOD-scid IL2rγnull) , NOD.Cg-Prkdcscid (abbreviated as NOD-scid)  and NOD.Cg-Prkdcscid Tg(HLA-A/H2-D/B2M)1Dvs/Dvs (abbreviated as NOD-scid HHD)  mice were obtained from The Jackson Laboratory (Bar Harbor, ME). NOD.Cg-Prkdcscid Il2rgtm1Wjl Tg(HLA-A/H2-D/B2M)1Dvs/DvsSz (abbreviated as NOD-scid IL2rγnull HHD) were generated by crossing NOD.Cg-Prkdcscid Il2rgtm1Wjl/Sz mice with NOD.Cg-Prkdcscid Tg(HLA-A/H2-D/B2M)1Dvs/Dvs and selecting for homozygosity of the Il2rγnull mutation and presence of the HHD transgene. HHD transgenics were maintained in a hemizygous fashion and evaluated for presence of the transgene by PCR or flow cytometry on peripheral blood before use in experiments. Mice at The University of Massachusetts Medical School and at The Jackson Laboratory were housed in a specific pathogen free facility in microisolator cages, and given autoclaved food and maintained on acidified autoclaved water and sulfamethoxazole/trimethoprim medicated water (Goldline Laboratories, Ft. Lauderdale, FL), provided on alternate weeks. All animal use was in accordance with the guidelines of the Institutional Animal Care and Use Committee (IACUC) of the University of Massachusetts Medical School and The Jackson Laboratory and conformed to the recommendations in the Guide for the Care and Use of Laboratory Animals.
Peptides were synthesized using Fmoc amino acids and PyBop/NMM chemistry. Synthetic peptides were analyzed by reversed phase HPLC (purity was at least 85%) and Maldi-Tof mass spectrometry (expected masses were confirmed). Tetrameric HLA-A2-peptide complexes were prepared as previously described .
Peripheral blood mononuclear cells (PBMCs) from a HLA-A*0201+ recent onset diabetic patient were incubated with A2/IGRP tetramer on ice. One hour later, cells were incubated with anti-CD8 for 20 min. A2/IGRP tetramer CD8 double-positive T-cells were sorted and seeded at one cell per well in 96-well plates, each well containing 1×105 irradiated (50 Gy) allogeneic PBMCs, 5×103 irradiated (100 Gy) IGRP265–273 peptide-pulsed HLA-A2-expressing EBV-LCL in IMDM supplemented with 10% HS, 0.5% LeucoA, 0.1 ng/ml rh-IL12, 10 ng/ml rh-IL7, 25 U/ml rh-IL2 and 5 ng/ml rh-IL15. T-cell clones were isolated and restimulated every 2–3 weeks as described above. Every 3–4 days fresh media containing 5 ng/ml IL-15 and 25 U/ml IL-2 were added. From the panel of IGRP-reactive CD8 T-cell clones, we selected one T-cell clone, termed clone 7 for further characterization.
To determine secretion of IFNγ, Granzyme B (GrB), and IL-10, 2×104 clone 7 cells were incubated with HLA-A2-expressing EBV-LCL pulsed with an IGRP-specific or a control peptide on anti-cytokine (IFNγ, GrB, and IL-10) antibody-precoated ELISA plates and after o/n culture in IMDM supplemented with 1% HS, plates were developed according to the manufacturer’s protocol (U-CyTech, Utrecht, the Netherlands). Results are expressed as means ± SD of triplicate wells.
Expression of CD107a on clone 7 cells was examined as described by Betts et al .
Total RNA was isolated using RNA BEE (Tel-Test, Friendswood, TX). Random-primed cDNA was synthesized according to manufacturer’s instructions (Roche, Indianapolis, IN). PCR amplification of cDNA was performed with Cα or Cß reverse primer (Cα: TgTgggAgATCTCTgCTTCTg,sequence Cß: TCCTTCCCATTCACCCACCAgCTCAgCTC in combination with a specific forward primer for Vα or Vß TCR ( for primer sequences). Control PCR amplifications for β-actin were performed with each sample to confirm cDNA integrity. Aliquots of each reaction were run on agarose gel prestained with ethidium bromide, in order to compare amplicon intensities between reactions. Appropriate dilutions were performed prior to analysis when necessary. To establish whether clone 7 cells were monoclonal, PCR products were subjected to nucleotide sequence analysis using ALFexpress sequencer (Pharmacia-Biotech, Sweden).
Standard 51Cr release assays were performed using HLA-A2+ EBV-LCL as target cells. Target cells were labeled with 51Cr (100 µCi, Perkin Elmer, Billerica, MA) in the absence or presence of 1 ug/ml specific or control peptide for 1 h at 37°C. After extensive washing, cells were suspended in IMDM/10% HS and 3000 labeled target cells were co-incubated at effector to target (E:T) ratios of 201, 51 and 11 in 96 well round-bottom plates in triplicate for 4 h at 37°C. Controls included target cells incubated in medium alone for spontaneous release and target cells in 5% (v/v) Triton X-100 (Sigma, St. Louis, MO) in PBS for maximum release. Radioactivity was measured by a Wallac Wizard 1470 Automatic Gamma Counter. The percentage of cytotoxic activity was calculated using the following formula: % specific lysis=(sample cpm–spontaneous cpm)/(maximal cpm–spontaneous cpm)×100%.
Cytotoxicity assays using intact mouse islets as targets were performed as described previously . Briefly, NOD-scid HHD and NOD-scid pancreatic islets (10 islets/well) were allowed to adhere in 96-well plates during a 10-day incubation at 37°C. Adherent islets were labeled with 5µCi/well of 51Cr for 3 h at 37°C. Islets were washed and overlaid with 100 µl of medium containing various numbers of cultured clone 7 cells. For establishing E:T ratios, each islet was assumed to contain 750 cells. A minimum of three wells were established for each E:T ratio. Spontaneous release controls consisted of nine wells of labeled islets from each donor cultured in the absence of T-cells. Following a 20 h incubation at 37°C, the radioactivity in two fractions from each well was measured. The first fraction was the culture supernatant, the second was obtained by solubilizing the remaining islets in 200 µl of 2% SDS. The percentage of 51Cr release for each well was calculated by the formula [(supernatant cpm)/(supernatant cpm + SDS lysate cpm)] x 100%. This allows normalization for variation in the sizes of individual islets, which could result in differences in the total levels of 51Cr incorporation in each well. In turn, percent-specific cytotoxicity was calculated by subtracting the percent 51Cr release from islets cultured in medium alone (i.e., spontaneous release) from the release by each well of islets cultured with a given number of T-cells.
To examine the cytotoxic potential of clone 7 cells in-vivo, an established in-vivo cytotoxicity assay was used with modifications ; . PBMC from HLA-A*0201+ healthy donors were labeled with either 2 µM or 0.2 µM CFSE (Sigma; CFSEhi and CFSElo cells, respectively) for 15 minutes at 37°C. CFSEhi cells were pulsed with 3 ug/ml IGRP265–273 peptide for 45 minutes at 37°C. CFSElo cells were pulsed with a control peptide. Both cell populations were washed, combined at equal ratios and 5×106 cells of each population were intravenously injected into NOD-scidIL2rγnull recipient mice via the tail vein. Recipient mice received intrasplenic injections of indicated numbers of clone 7 IGRP-specific CD8 T cells or control T-cells 24 h earlier. Spleens from recipient mice were harvested 20 hours after target cell injection, and survival of each transferred population was assessed by flow cytometry. A minimum of 1×103 CFSE+ events were collected from each sample. Specific cytolytic activity was calculated using the following equation: [1– [(CFSEhi/CFSElo in IGRP-T-cell recipients)/(CFSEhi/CFSElo in control T-cell recipients)]×100.
NOD-scid IL2rγnull HHD recipient mice were injected i.v. with 20×106 PBMC from a HLA-A*0201+ healthy donor. Two days later, mice were injected intra-pancreatically with 5×106 clone 7 cells, 5×106 control tumor-antigen specific T-cells (PRAME-specific T-cell clone) or sham injected. Blood glucose levels were monitored twice weekly. After 4 weeks, pancreata were recovered for histological analysis. Paraffin-embedded tissues were sectioned at 4 µm and stained with hematoxylin and eosin (H&E) or used for immunohistochemistry. Immune-stained tissues utilized antibodies with specificity for insulin, human CD45 (DAKO, Carpinteria, CA), and employed a standard avidin–biotin complex methodology . The sections were developed using 3-diaminobenzidine and counterstained with hematoxylin for light microscopic visualization. Alternatively, sections were incubated with guinea pig anti-insulin that was visualized by staining with anti-guinea pig IgG conjugated toAlexa-488 and rabbit anti-Caspase-3 antibody that was visualized by staining with anti-rabbit IgG conjugated to Alexa-594 (Invitrogen). Nuclei were visualized with DAPI and the stain sections were analyzed using immunofluorescence microscopy. Control protocols included omission of primary antibodies and the use of species-matched nonbinding control antibodies.
Experimental groups were compared to controls using student’s t-test. P<0.05 was considered significant.
IGRP265–273 specifically binds to HLA-A2. Peptide binding to HLA-A1, -A2, -A3 and –B8 was assessed using a competition based binding assay . The percentage of fluorescent-labeled reference peptide bound to a specific HLA-allele at different concentrations of unlabeled IGRP265–273 peptide is shown. The IC50 value defines the concentration of IGRP265–273 peptide needed to inhibit 50% binding of the fluorescent-labeled reference peptide. IC50 value HLA-A263 nM; IC50 value HLA-A1, HLA-A3, HLA-B812590 nM.
IGRP-specific T-cells express adhesion molecules important for migration into inflamed pancreas and secondary lymphoid tissue. IGRP-specific T-cells were stained with antibodies against TCRαβ, CD2, CD28, HLA-DR, CD45RA, CD45RO, CXCR3, CCR4, CCR5, CCR7, CCR7 and CD62L and analyzed by flow cytometry. Dashed lines represent isotype antibody staining, solid lines represent specific antibody staining. These results are representation of 3 experiments.
Clone 7 IGRP/A2 binding T-cells cloned from a type 1 diabetic individual are clonal. Clonality of IGRP-specific clone 7 T-cells was determined by examining expression of TCR Vα and TCR Vβ chains. Specific PCR with Cα or Cß reverse primer in combination with a specific forward primer for Vα or Vß TCR revealed expression of Vβ13c and Vα19 transcripts in clone 7 T-cells. Control PCR amplifications for β-actin were performed for each sample to confirm cDNA integrity. Total RNA was isolated using RNA BEE (Tel-Test, Friendswood, TX). Random-primed cDNA was synthesized according to manufacturer’s instructions (Roche, Indianapolis, IN). PCR amplification of cDNA was performed with Cα or Cß reverse primer (Cα: TgTgggAg-ATCTCTgCTTCTg, sequence Cß: TCCTTCCCATTCACCCACCAgCTCAgCTC in combination with a specific forward primer for Vα or Vß TCR ( for primer sequences). Control PCR amplifications for β-actin were performed with each sample to confirm cDNA integrity. Aliquots of each reaction were run on agarose gel prestained with ethidium bromide, in order to compare amplicon intensities between reactions. Appropriate dilutions were performed prior to analysis when necessary. To establish whether clone 7 cells were monoclonal, PCR products were subjected to nucleotide sequence analysis using ALFexpress sequencer (Pharmacia-Biotech, Sweden).
We thank Prof P. van der Bruggen and Dr. N. Demotte (Ludwig Institute for Cancer Research, 74 av. Hippocrate, UCL7459, B-1200 Brussels, Belgium) for generation of and helpful suggestions using the mutant tetramers.
This study has been supported in part by grants from the Juvenile Diabetes Research Foundation Program Grant (7-2005-877 to BOR, WWJU, SL and JWD), the Dutch Diabetes Research Foundation DFN (to JRFA), National Institutes of Health Grant AI46629 (and an institutional Diabetes Endocrinology Research Center (DERC) grant DK32520, the Beta Cell Biology Consortium, a grant from the Helmsley Foundation and the Dutch Diabetes Research Foundation. BOR is recipient of a VICI award (ZonMW). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.