A molecular basis for the association of the HLA-DRB1 locus, citrullination, and rheumatoid arthritis

SW Scally, J Petersen, SC Law, NL Dudek… - Journal of Experimental …, 2013 - rupress.org
SW Scally, J Petersen, SC Law, NL Dudek, HJ Nel, KL Loh, LC Wijeyewickrema, SBG Eckle
Journal of Experimental Medicine, 2013rupress.org
Rheumatoid arthritis (RA) is strongly associated with the human leukocyte antigen (HLA)-
DRB1 locus that possesses the shared susceptibility epitope (SE) and the citrullination of
self-antigens. We show how citrullinated aggrecan and vimentin epitopes bind to HLA-
DRB1* 04: 01/04. Citrulline was accommodated within the electropositive P4 pocket of HLA-
DRB1* 04: 01/04, whereas the electronegative P4 pocket of the RA-resistant HLA-DRB1*
04: 02 allomorph interacted with arginine or citrulline-containing epitopes. Peptide elution …
Rheumatoid arthritis (RA) is strongly associated with the human leukocyte antigen (HLA)-DRB1 locus that possesses the shared susceptibility epitope (SE) and the citrullination of self-antigens. We show how citrullinated aggrecan and vimentin epitopes bind to HLA-DRB1*04:01/04. Citrulline was accommodated within the electropositive P4 pocket of HLA-DRB1*04:01/04, whereas the electronegative P4 pocket of the RA-resistant HLA-DRB1*04:02 allomorph interacted with arginine or citrulline-containing epitopes. Peptide elution studies revealed P4 arginine–containing peptides from HLA-DRB1*04:02, but not from HLA-DRB1*04:01/04. Citrullination altered protease susceptibility of vimentin, thereby generating self-epitopes that are presented to T cells in HLA-DRB1*04:01+ individuals. Using HLA-II tetramers, we observed citrullinated vimentin- and aggrecan-specific CD4+ T cells in the peripheral blood of HLA-DRB1*04:01+ RA-affected and healthy individuals. In RA patients, autoreactive T cell numbers correlated with disease activity and were deficient in regulatory T cells relative to healthy individuals. These findings reshape our understanding of the association between citrullination, the HLA-DRB1 locus, and T cell autoreactivity in RA.
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