The SAgA of Antigen-Specific Immunotherapy for Type 1 Diabetes

Abstract

Islet antigen-specific strategies are the holy grail of immunotherapy for type 1 diabetes (T1D) (1), as they selectively target the autoimmune responses involved in b-cell destruction (2). The idea is to induce a response opposite to that of a conventional vaccine. The administration of antigen(s) in the absence of inflammation (e.g., adjuvants) should potentiate the outcomes of physiological immune homeostasis, i.e., anergy, regulatory polarization, and, to a lesser extent, deletion. Such antigens can be delivered as proteins, peptides, bacteria engineered to secrete these products, DNA plasmids, or nanoparticles coated with antigens (either alone or preloaded on MHC molecules). Peptides are easy to synthesize by amino acid chemistry, but they are variably water-soluble and shortlived in vivo (in the order of minutes), which makes it difficult to achieve the steady concentrations more suitable for tolerance induction. Nonetheless, peptide-based immunotherapies have proven safe and, in some cases, documented encouraging immune and clinical outcomes (3). In this issue of Diabetes, Firdessa-Fite et al. (4) give peptides a boost by mounting them on a hyaluronan backbone to obtain a soluble antigen array (SAgA). First, this backbone accounts for their superior solubility. The linker used was either stable (“click” chemistry, cSAgA) or hydrolysable (hSAgA), to facilitate peptide release upon uptake by antigen-presenting cells (APCs). Second, SAgAs deliver multiple peptide copies to individual APCs, thus providing a multivalent (high avidity) engagement of T cells that is more efficient for signal transduction. This may be critical for the low-affinity T cells involved in autoimmunity. A gradient of biodistribution was observed in draining lymph nodes proximal or distal to the interscapular subcutaneous immunization site, which raises the question of whether sites closer to pancreatic lymph nodes (5) may achieve superior effects. Thymic delivery may also deserve attention (6,7). SAgAs were loaded with either the hybrid peptide 2.5HIP, which is the natural antigen ligand of diabetogenic BDC2.5 CD4 T cells (8), or with its more potent p79 mimotope. Contrary to free peptides, these SAgAs efficiently prevented diabetes in NOD mice only when used in combination. While this may reflect the need to achieve a critical quantitative threshold of T cells targeted, a synergistic functional effect is plausible. Indeed, 2.5HIPreactive and p79-reactive T cells, which were, surprisingly, distinct populations, underwent different outcomes upon treatment with their cognate SAgA (Fig. 1). IL-10 T regulatory (Tr)1 cells were induced by the more potent p79 ligand, while Foxp3 Tregs were amplified, but not de novo induced, by the weaker (and less soluble) 2.5HIP. These effects were dose-dependent, as SAgAs induced Tr1 cells at higher dose and Foxp3 Tregs at lower dose. SAgAs promoted more effective and persistent engagement and expansion of autoreactive T cells than free peptides in vivo, with no deletional effect observed. Critically, SAgAs were stronger inducers of tolerance-associated markers, including decreased CD44 expression and increased CD73/FR4, Lag-3, PD-1, and KLRG-1, suggestive of anergic/regulatory/exhausted phenotypes. The cSAgA formulation proved superior to hSAgA at inducing CD73/ FR4, PD-1, and IL-10, at preventing diabetes, and at avoiding anaphylaxis (likely as a result of decreased shedding of free peptides). Although NOD mice are particularly prone to peptide-induced anaphylaxis (9), this issue is critical in the allergy setting but probably less so in human T1D. Originally described after insulin B9-23 peptide immunization in NOD mice (10), such reactions were not observed, despite Th2 polarization, in a small-scale human trial with a similar peptide (11), and in other peptide-based intervention trials. Some questions are open for further investigation, including whether the therapeutic outcome is IL-10–dependent, the role of B-cell and CD8 T-cell tolerance, the need for continuous treatment, the efficacy at inducing diabetes remission, and human T-cell studies in vitro and/or in humanized mice. Although the peptides to load