Beta cell antigens in type 1 diabetes: triggers in pathogenesis and therapeutic targets

F1000Res. 2016 Apr 22:5:F1000 Faculty Rev-728. doi: 10.12688/f1000research.7411.1. eCollection 2016.

Abstract

Research focusing on type 1 diabetes (T1D) autoantigens aims to explore our understanding of these beta cell proteins in order to design assays for monitoring the pathogenic autoimmune response, as well as safe and efficient therapies preventing or stopping it. In this review, we will discuss progress made in the last 5 years with respect to mechanistic understanding, diagnostic monitoring, and therapeutic modulation of the autoantigen-specific cellular immune response in T1D. Some technical progress in monitoring tools has been made; however, the potential of recent technologies for highly multiplexed exploration of human cellular immune responses remains to be exploited in T1D research, as it may be the key to the identification of surrogate markers of disease progression that are still wanting. Detailed analysis of autoantigen recognition by T cells suggests an important role of non-conventional antigen presentation and processing in beta cell-directed autoimmunity, but the impact of this in human T1D has been little explored. Finally, therapeutic administration of autoantigens to T1D patients has produced disappointing results. The application of novel modes of autoantigen administration, careful translation of mechanistic understanding obtained in preclinical studies and in vitro with human cells, and combination therapies including CD3 antibodies may help to make autoantigen-based immunotherapy for T1D a success story in the future.

Keywords: Antigen-based immunotherapy; Beta Cell Antigen; Type 1 Diabetes; autoreactive T cells; insulin recognition.

Publication types

  • Review

Grants and funding

Work in the authors’ laboratory is supported by grants from Fondation pour la Recherche Médicale (DEQ20130326539) and Idex Sorbonne Paris Cité to PvE, by a grant from Aide aux Jeunes Diabétiques to FXM and PvE, and by grants from EFSD-Lilly and from the Juvenile Diabetes Research Foundation (47-2013-524 and 2-SRA-2015-73) to JD.