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Cytotoxic CD8+ T cells target citrullinated antigens in rheumatoid arthritis

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Listed:
  • Jae-Seung Moon

    (Stanford University School of Medicine
    VA Palo Alto Health Care System)

  • Shady Younis

    (Stanford University School of Medicine
    VA Palo Alto Health Care System
    Stanford University)

  • Nitya S. Ramadoss

    (Stanford University School of Medicine
    VA Palo Alto Health Care System)

  • Radhika Iyer

    (Stanford University School of Medicine
    VA Palo Alto Health Care System)

  • Khushboo Sheth

    (Stanford University School of Medicine
    VA Palo Alto Health Care System)

  • Orr Sharpe

    (Stanford University School of Medicine
    VA Palo Alto Health Care System)

  • Navin L. Rao

    (Janssen Research and Development LLC)

  • Stephane Becart

    (Janssen Research and Development LLC)

  • Julie A. Carman

    (Janssen Research and Development LLC)

  • Eddie A. James

    (Center for Translational Immunology, Benaroya Research Institute)

  • Jane H. Buckner

    (Center for Translational Immunology, Benaroya Research Institute)

  • Kevin D. Deane

    (University of Colorado Anschutz Medical Campus)

  • V. Michael Holers

    (University of Colorado Anschutz Medical Campus)

  • Susan M. Goodman

    (Hospital for Special Surgery
    Weill Cornell Medicine)

  • Laura T. Donlin

    (Hospital for Special Surgery
    Weill Cornell Medicine)

  • Mark M. Davis

    (Stanford University
    Stanford University)

  • William H. Robinson

    (Stanford University School of Medicine
    VA Palo Alto Health Care System
    Stanford University)

Abstract

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.

Suggested Citation

  • Jae-Seung Moon & Shady Younis & Nitya S. Ramadoss & Radhika Iyer & Khushboo Sheth & Orr Sharpe & Navin L. Rao & Stephane Becart & Julie A. Carman & Eddie A. James & Jane H. Buckner & Kevin D. Deane & , 2023. "Cytotoxic CD8+ T cells target citrullinated antigens in rheumatoid arthritis," Nature Communications, Nature, vol. 14(1), pages 1-15, December.
  • Handle: RePEc:nat:natcom:v:14:y:2023:i:1:d:10.1038_s41467-022-35264-8
    DOI: 10.1038/s41467-022-35264-8
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    References listed on IDEAS

    as
    1. P. Savola & T. Kelkka & H. L. Rajala & A. Kuuliala & K. Kuuliala & S. Eldfors & P. Ellonen & S. Lagström & M. Lepistö & T. Hannunen & E. I. Andersson & R. K. Khajuria & T. Jaatinen & R. Koivuniemi & H, 2017. "Somatic mutations in clonally expanded cytotoxic T lymphocytes in patients with newly diagnosed rheumatoid arthritis," Nature Communications, Nature, vol. 8(1), pages 1-14, August.
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