细胞毒性 CD8 T 细胞靶向类风湿关节炎中的瓜氨酸化抗原。

Cytotoxic CD8 T cells target citrullinated antigens in rheumatoid arthritis.

机构信息

Division of Immunology and Rheumatology, Department of Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.

VA Palo Alto Health Care System, Palo Alto, CA, 94304, USA.

出版信息

Nat Commun. 2023 Jan 19;14(1):319. doi: 10.1038/s41467-022-35264-8.

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 GZMBCD8 subpopulations containing large clonal lineage expansions that express cytotoxic and tissue homing transcriptional programs, while a GZMKCD8 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 GZMBCD8 T cells to expand, express cytotoxic mediators, and mediate killing of target cells. We also demonstrate that these clonally expanded GZMBCD8 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.

摘要

介导类风湿关节炎(RA)滑膜炎和关节破坏的免疫机制仍未完全明确。尽管在 RA 患者中已经描述了 CD8 T 细胞水平的升高,但它们在发病机制中的功能仍不清楚。在这里,我们对源自抗瓜氨酸化蛋白抗体(ACPA)+ RA 血液的 CD8 T 细胞进行了单细胞转录组和 T 细胞受体(TCR)测序。我们鉴定了含有大克隆谱系扩增的 GZMBCD8 亚群,这些亚群表达细胞毒性和组织归巢转录程序,而 GZMKCD8 记忆亚群包含表达效应 T 细胞转录程序的较小克隆扩增。我们证明 RA 瓜氨酸化自身抗原由 MHC I 类呈递,激活 RA 血液来源的 GZMBCD8 T 细胞扩增,表达细胞毒性介质,并介导靶细胞的杀伤。我们还证明这些克隆扩增的 GZMBCD8 细胞存在于 RA 滑膜中。这些发现表明,针对瓜氨酸化抗原的细胞毒性 CD8 T 细胞有助于 ACPA+ RA 的滑膜炎和关节组织破坏。

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