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Peptide-based treatment for autoimmune diseases: learning how to handle a double-edged sword
Alberto Pugliese
Departments of Medicine, and Immunology and Microbiology, Immunogenetics Program, Diabetes Research Institute, University of Miami, Miami, Florida, USA
Address correspondence to: Alberto Pugliese, Departments of Medicine, and Immunology and Microbiology, Immunogenetics Program, Diabetes Research Institute, University of Miami, 1450 NW Tenth Avenue, Miami, Florida 33136, USA. Phone (305) 243-5348; Fax: (305) 243-4404; E-mail: apuglies@med.miami.edu.
Find articles by Pugliese, A. in: JCI | PubMed | Google Scholar
Published May 1, 2003 - More info
J Clin Invest. 2003;111(9):1280–1282. https://doi.org/10.1172/JCI18395.
© 2003 The American Society for Clinical Investigation
Several self-molecules have been identified as target antigens in autoimmune diseases. Since lack or loss of tolerance to these molecules is one of the key events promoting autoimmunity, researchers are exploring the possibility that the administration of antigens or peptides may stimulate tolerogenic mechanisms and delay or prevent the full phenotypic expression of autoimmune diseases. There is much enthusiasm for such therapies, as these will probably be disease-specific and not associated with the side effects of conventional immunosuppression. Studies have been performed and are ongoing in both rodents and humans, using whole antigens or peptides, and testing diverse administration routes such as intrathymic, intraperitoneal, intravenous, subcutaneous, oral, and intranasal. Despite many studies, robust data demonstrating clinical benefits are not yet available (1).
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The double-edged sword
In the current issue of the JCI, Martinez et al. report on a new element that will need to be considered when attempting peptide-based T1D therapy (18). While the goal of peptide administration is to induce regulatory cells and inhibit specific autoimmune responses, the data show that, depending on the peptide used, one may also induce undesired cytotoxic CD8+ T cell responses. In this study, the intranasal administration of the B24–C36 proinsulin peptide to NOD mice induced regulatory cells that could transfer disease protection to another mouse, but the peptide-treated mice were not protected from developing spontaneous disease. The authors then noted that the B24–C36 peptide contains binding motifs not only for I-Ag7, the MHC class II molecule of the NOD mouse, but also for the MHC class I molecule Kd. The B24–C36 peptide contains the B25–C34 and B26–C34 epitopes that bind to Kd, and mice immunized with the latter two peptides mounted specific cytotoxic responses. In contrast, the systemic administration of B25–C34 reduced spontaneous diabetes incidence, confirming a role for CD8+ responses to this epitope in the natural disease process. Thus, intranasal administration of the B24–C36 peptide resulted in both regulatory CD4+ T cell and cytotoxic CD8+ T cell responses recognizing the Kd-restricted B25–C34 epitope contained in the B24–C36 peptide. Such cytotoxic responses blunted the protective effect associated with the induction of the regulatory cells, suggesting that mucosal administration of antigen can sometimes be a double-edged sword. To circumvent this problem, the authors designed a strategy to “disable” the CD8+ epitope contained in the B24–C36 peptide, in other words, to prevent CD8+ T cells from recognizing this epitope, while preserving the ability to induce regulatory CD4+ T cells (Figure 1 and Table 1). This was achieved by treating the mice with truncated peptides, B24–C33 or B24–C32, still capable of binding to IAg7 but not to Kd. Intranasal administration of the truncated peptides resulted indeed in a significant reduction in the incidence of spontaneous diabetes.
Figure 1Disabling a CD8+ epitope. Intranasal administration of different proinsulin peptides results in presentation from an antigen-presenting cell (APC) to CD4+ and CD8+ T cells, depending on the peptide administered. Proinsulin peptides B24–C36, B24–C35, and B26–C34 can bind to the MHC class I molecule (Kd), resulting in the activation of cytotoxic T cells. The use of truncated peptides that do not contain the residues critical for binding to Kd, but still bind to the NOD mouse MHC class II molecule (I-Ag7), allows for selective activation of regulatory CD4+ T cells. The same APC is shown presenting simultaneously to both CD4+ and CD8+ T cells for illustration purposes. TCR, T cell receptor.
Table 1Key proinsulin peptides, their respective MHC binding capacities, and induced T cell responses
The findings reported by Martinez et al. (18) suggest that the undetected induction of CD8+ T cell responses could explain at least some of the contrasting outcomes reported by several experimental studies and clinical trials. Most importantly, this study has practical implications for the design of clinical trials based on the administration of peptides for preventing autoimmunity. Based on these findings, it would seem helpful to select putative therapeutic peptides for their ability to selectively bind class II but not class I molecules that are used as restriction elements by CD8+ T cells and could potentially antagonize the beneficial effects of class II–restricted, regulatory CD4+ T cells. This strategy can effectively disable the potential of eliciting cytotoxic responses and maximize the protective effects of the regulatory cells. While this study was limited to the NOD mouse MHC molecules, the availability of mouse strains expressing human class II and class I molecules (19–21), in particular those associated with T1D susceptibility, is increasing. This offers researchers the opportunity to test such binding predictions and may provide an in vivo readout of the responses induced by a given peptide also in relation to dose and route of administration. Screening of candidate peptides for clinical trials using such humanized mouse models could guide the choice of peptides for future prevention trials and might maximize our chances of achieving both efficacy and safety.
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