HLA class I hyper-expression unmasks beta cells but not alpha cells to the immune system in pre-diabetes

J Autoimmun. 2021 May:119:102628. doi: 10.1016/j.jaut.2021.102628. Epub 2021 Mar 9.

Abstract

Human leukocyte antigens of class-I (HLA-I) molecules are hyper-expressed in insulin-containing islets (ICI) of type 1 diabetic (T1D) donors. This study investigated the HLA-I expression in autoantibody positive (AAB+) donors and defined its intra-islet and intracellular localization as well as proximity to infiltrating CD8 T cells with high-resolution confocal microscopy. We found HLA-I hyper-expression had already occurred prior to clinical diagnosis of T1D in islets of AAB+ donors. Interestingly, throughout all stages of disease, HLA-I was mostly expressed by alpha cells. Hyper-expression in AAB+ and T1D donors was associated with intra-cellular accumulation in the Golgi. Proximity analysis showed a moderate but significant correlation between HLA-I and infiltrating CD8 T cells only in ICI of T1D donors, but not in AAB+ donors. These observations not only demonstrate a very early, islet-intrinsic immune-independent increase of HLA-I during diabetes pathogenesis, but also point towards a role for alpha cells in T1D.

Keywords: Alpha cells; Beta cells; HLA class I; Type 1 diabetes; nPOD.

Publication types

  • Research Support, N.I.H., Extramural
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Autoantibodies / immunology
  • Autoantigens / immunology
  • Autoimmunity
  • Biomarkers
  • Diabetes Mellitus, Type 1 / etiology
  • Diabetes Mellitus, Type 1 / metabolism
  • Disease Susceptibility / immunology
  • Fluorescent Antibody Technique
  • Gene Expression*
  • Glucagon-Secreting Cells / metabolism*
  • Histocompatibility Antigens Class I / genetics*
  • Histocompatibility Antigens Class I / immunology*
  • Humans
  • Insulin-Secreting Cells / immunology*
  • Insulin-Secreting Cells / metabolism*
  • Islets of Langerhans / immunology
  • Islets of Langerhans / metabolism
  • Islets of Langerhans / pathology
  • Prediabetic State / etiology*
  • Prediabetic State / immunology*
  • Protein Transport
  • T-Lymphocyte Subsets / immunology
  • T-Lymphocyte Subsets / metabolism

Substances

  • Autoantibodies
  • Autoantigens
  • Biomarkers
  • Histocompatibility Antigens Class I