Shared recognition of citrullinated tenascin-C peptides by T and B cells in rheumatoid arthritis

类风湿性关节炎中T细胞和B细胞对瓜氨酸化腱生蛋白-C肽的共同识别

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作者:Jing Song ,Anja Schwenzer ,Alicia Wong ,Sara Turcinov ,Cliff Rims ,Lorena Rodriguez Martinez ,David Arribas-Layton ,Christina Gerstner ,Virginia S Muir ,Kim S Midwood ,Vivianne Malmström ,Eddie A James ,Jane H Buckner

Abstract

Tenascin-C (TNC), an extracellular matrix protein that has proinflammatory properties, is a recently described antibody target in rheumatoid arthritis (RA). In this study, we utilized a systematic discovery process and identified 5 potentially novel citrullinated TNC (cit-TNC) T cell epitopes. CD4+ T cells specific for these epitopes were elevated in the peripheral blood of subjects with RA and showed signs of activation. Cit-TNC-specific T cells were also present among synovial fluid T cells and secreted IFN-γ. Two of these cit-TNC T cell epitopes were also recognized by antibodies within the serum and synovial fluid of individuals with RA. Detectable serum levels of cit-TNC-reactive antibodies were prevalent among subjects with RA and positively associated with cyclic citrullinated peptide (CCP) reactivity and the HLA shared epitope. Furthermore, cit-TNC-reactive antibodies were correlated with rheumatoid factor and elevated in subjects with a history of smoking. This work confirms cit-TNC as an autoantigen that is targeted by autoreactive CD4+ T cells and autoantibodies in patients with RA. Furthermore, our findings raise the possibility that coinciding epitopes recognized by both CD4+ T cells and B cells have the potential to amplify autoimmunity and promote the development and progression of RA.

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