Laboratory of Translational Immunology, University Medical Centre Utrecht, Wilhelmina Children's Hospital, Lundlaan 6, 3508 AB Utrecht, Netherlands.
Nat Rev Rheumatol. 2016 Jul;12(7):421-8. doi: 10.1038/nrrheum.2016.74. Epub 2016 Jun 3.
CD8(+) T cells are key players in the body's defence against viral infections and cancer. To date, data on the role of CD8(+) T cells in autoimmune diseases have been scarce, especially when compared with the wealth of research on CD4(+) T cells. However, growing evidence suggests that CD8(+) T-cell homeostasis is impaired in human autoimmune diseases. The contribution of CD8(+) T cells to autoimmune arthritis is indicated by the close association of MHC class I polymorphisms with disease risk, as well as the correlation between CD8(+) T-cell phenotype and disease outcome. The heterogeneous phenotype, resistance to regulation and impaired regulatory function of CD8(+) T cells - especially at the target organ - might contribute to the persistence of autoimmune inflammation. Moreover, newly identified populations of tissue-resident CD8(+) T cells and their interaction with antigen-presenting cells might have a key role in disease pathology. In this Review, we assess the link between CD8(+) T cells, autoimmune arthritis and the basis of their homeostatic changes under inflammatory conditions. Improved insight into CD8(+) T cell-specific pathogenicity will be essential for a better understanding of autoimmune arthritis and the identification of new therapeutic targets.
CD8(+) T 细胞是人体抵御病毒感染和癌症的关键因素。迄今为止,关于 CD8(+) T 细胞在自身免疫性疾病中的作用的数据还很缺乏,尤其是与大量关于 CD4(+) T 细胞的研究相比。然而,越来越多的证据表明,CD8(+) T 细胞的稳态在人类自身免疫性疾病中受到损害。MHC Ⅰ类多态性与疾病风险密切相关,以及 CD8(+) T 细胞表型与疾病结局之间的相关性,表明 CD8(+) T 细胞对自身免疫性关节炎有贡献。CD8(+) T 细胞的异质性表型、对调节的抵抗和受损的调节功能——尤其是在靶器官——可能导致自身免疫性炎症的持续存在。此外,新发现的组织驻留 CD8(+) T 细胞群体及其与抗原呈递细胞的相互作用可能在疾病发病机制中发挥关键作用。在这篇综述中,我们评估了 CD8(+) T 细胞、自身免疫性关节炎以及在炎症条件下其稳态变化的基础之间的联系。深入了解 CD8(+) T 细胞的特异性致病性对于更好地理解自身免疫性关节炎和确定新的治疗靶点至关重要。