| Literature DB >> 30402774 |
Stuart I Mannering1,2, Anthony R Di Carluccio3, Colleen M Elso3,4.
Abstract
Type 1 diabetes is an autoimmune disease caused by T cell-mediated destruction of pancreatic insulin-producing beta cells. The epitopes recognised by pathogenic T cells in human type 1 diabetes are poorly defined; however, a growing body of evidence suggests that T cell responses against neoepitopes contribute to beta cell destruction in type 1 diabetes. Neoepitopes are formed when self-proteins undergo post-translational modification to create a new epitope that is recognised by T- or B cells. Here we review the role of human T cell responses against neoepitopes in the immune pathogenesis of type 1 diabetes. Specifically, we review the different approaches to identifying neoepitopes relevant to human type 1 diabetes and outline several advances in this field that have occurred over the past few years. We also discuss the application of neoepitopes to the development of antigen-specific therapies for type 1 diabetes and the unresolved challenges that need to be overcome before the full repertoire of neoepitopes recognised by pathogenic human T cells in type 1 diabetes can be determined. This information may then be used to develop antigen-specific therapies for type 1 diabetes and assays to monitor changes in pathogenic, beta cell-specific T cell responses.Entities:
Keywords: Antigen-specific therapy; Beta cells; Hybrid insulin peptides; Neoepitopes; Post-translational modification; Review; T cells; Type 1 diabetes
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Year: 2018 PMID: 30402774 DOI: 10.1007/s00125-018-4760-6
Source DB: PubMed Journal: Diabetologia ISSN: 0012-186X Impact factor: 10.122