Predominant occupation of the MHC class I MHC molecule H-2Kwm7 with a single self peptide suggest a mechanism for its diabetes-protective effect.

Brims, Daniel R. and Qian, Jie and Jarchum, Irene and Mikesh, Leann and Palmieri, Edith and Ramagopal, Udupi A. and Malashkevich, Vladimir N. and Chaparro, Rodolfo J. and Lund, Torben and Hattori, Masakazu and Shabanowitz, Jeffrey and Hunt, Donald F. and Nathenson, Stanley G. and Almo, Steven C. and DiLorenzo, Teresa P. (2010) Predominant occupation of the MHC class I MHC molecule H-2Kwm7 with a single self peptide suggest a mechanism for its diabetes-protective effect. International Immunology, 22 (3). pp. 191-203. ISSN 0953-8178

Full text is not in this repository.

This item is available in the Library Catalogue

Abstract

Type 1 diabetes (T1D) is an autoimmune disease characterized by T cell-mediated destruction of insulin-producing pancreatic β cells. In both humans and the non-obese diabetic (NOD) mouse model of T1D, class II MHC alleles are the primary determinant of disease susceptibility. However, class I MHC genes also influence risk. These findings are consistent with the requirement for both CD4+ and CD8+ T cells in the pathogenesis of T1D. Although a large body of work has permitted the identification of multiple mechanisms to explain the diabetes-protective effect of particular class II MHC alleles, studies examining the protective influence of class I alleles are lacking. Here, we explored this question by performing biochemical and structural analyses of the murine class I MHC molecule H-2Kwm7, which exerts a diabetes-protective effect in NOD mice. We have found that H-2Kwm7 molecules are predominantly occupied by the single self-peptide VNDIFERI, derived from the ubiquitous protein histone H2B. This unexpected finding suggests that the inability of H-2Kwm7 to support T1D development could be due, at least in part, to the failure of peptides from critical β-cell antigens to adequately compete for binding and be presented to T cells. Predominant presentation of a single peptide would also be expected to influence T-cell selection, potentially leading to a reduced ability to select a diabetogenic CD8+ T-cell repertoire. The report that one of the predominant peptides bound by T1D-protective HLA-A*31 is histone derived suggests the potential translation of our findings to human diabetes-protective class I MHC molecules.

Item Type:Article
Research Areas:Middlesex University Schools and Centres > School of Science and Technology > Natural Sciences
ID Code:6690
Useful Links:
Deposited On:09 Nov 2010 15:00
Last Modified:10 Oct 2013 09:55

Repository staff only: item control page

Full text downloads (NB count will be zero if no full text documents are attached to the record)

Downloads per month over the past year