Cytotoxic CD8<sup>+</sup> T cells target citrullinated antigens in rheumatoid arthritis.

Moon, Jae-Seung; Younis, Shady; Ramadoss, Nitya S; Iyer, Radhika; Sheth, Khushboo; Sharpe, Orr; Rao, Navin L; Becart, Stephane et al. · Nat Commun · 2023

basic_science · Level V

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Abstract

The immune mechanisms that mediate synovitis and joint destruction in rheumatoid arthritis (RA) remain poorly defined. Although increased levels of CD8<sup>+</sup> 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<sup>+</sup> T cells derived from anti-citrullinated protein antibodies (ACPA)+ RA blood. We identify GZMB<sup>+</sup>CD8<sup>+</sup> subpopulations containing large clonal lineage expansions that express cytotoxic and tissue homing transcriptional programs, while a GZMK<sup>+</sup>CD8<sup>+</sup> 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<sup>+</sup>CD8<sup>+</sup> T cells to expand, express cytotoxic mediators, and mediate killing of target cells. We also demonstrate that these clonally expanded GZMB<sup>+</sup>CD8<sup>+</sup> cells are present in RA synovium. These findings suggest that cytotoxic CD8<sup>+</sup> T cells targeting citrullinated antigens contribute to synovitis and joint tissue destruction in ACPA+ RA.

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