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

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 prox...

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Veröffentlicht in:Journal of autoimmunity 2021-05, Vol.119, p.102628-102628, Article 102628
Hauptverfasser: Benkahla, Mehdi A., Sabouri, Somayeh, Kiosses, William B., Rajendran, Sakthi, Quesada-Masachs, Estefania, von Herrath, Matthias G.
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Sprache:eng
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Zusammenfassung: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. •HLA-I was hyperexpressed in autoantibody positive (AAB+) patients prior to clinical diagnosis of T1D.•HLA-I was mostly expressed by alpha cells irrespective of disease status.•In islets of AAB+ and T1D donors, HLA-I accumulates in the Golgi compartment.•A significant correlation between HLA-I and infiltrating CD8 T cells in insulin-containing islets of T1D donors.
ISSN:0896-8411
1095-9157
DOI:10.1016/j.jaut.2021.102628