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Cytotoxic CD8 + T cells target citrullinated antigens in rheumatoid arthritis.

Jae-Seung MoonShady YounisNitya S RamadossRadhika IyerKhushboo ShethOrr SharpeNavin L RaoStephane BecartJulie A CarmanEddie A JamesJane H BucknerKevin D DeaneV Michael HolersSusan M GoodmanLaura T DonlinMark M DavisWilliam H Robinson
Published in: Nature communications (2023)
The immune mechanisms that mediate synovitis and joint destruction in rheumatoid arthritis (RA) remain poorly defined. Although increased levels of CD8 + T cells have been described in RA, their function in pathogenesis remains unclear. Here we perform single cell transcriptome and T cell receptor (TCR) sequencing of CD8 + T cells derived from anti-citrullinated protein antibodies (ACPA)+ RA blood. We identify GZMB + CD8 + subpopulations containing large clonal lineage expansions that express cytotoxic and tissue homing transcriptional programs, while a GZMK + CD8 + memory subpopulation comprises smaller clonal expansions that express effector T cell transcriptional programs. We demonstrate RA citrullinated autoantigens presented by MHC class I activate RA blood-derived GZMB + CD8 + T cells to expand, express cytotoxic mediators, and mediate killing of target cells. We also demonstrate that these clonally expanded GZMB + CD8 + cells are present in RA synovium. These findings suggest that cytotoxic CD8 + T cells targeting citrullinated antigens contribute to synovitis and joint tissue destruction in ACPA+ RA.
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