The University of Queensland Diamantina Institute, Translational Research Institute, Princess Alexandra Hospital, Brisbane, Australia.
King's College London, Academic Department of Rheumatology, Centre for Inflammation Biology and Cancer Immunology, School of Immunology and Microbial Sciences, Faculty of Life Sciences and Medicine, London, UK.
Clin Exp Immunol. 2019 Apr;196(1):12-27. doi: 10.1111/cei.13256. Epub 2019 Jan 21.
Dendritic cells (DCs) are the key professional antigen-presenting cells which bridge innate and adaptive immune responses, inducing the priming and differentiation of naive to effector CD4 T cells, the cross-priming of CD8 T cells and the promotion of B cell antibody responses. DCs also play a critical role in the maintenance of immune homeostasis and tolerance. DC-T cell interactions underpin the generation of an autoimmune response in rheumatoid arthritis (RA). Here we describe the function of DCs and review evidence for DC and T cell involvement in RA pathogenesis, in particular through the presentation of self-peptide by DCs that triggers differentiation and activation of autoreactive T cells. Finally, we discuss the emerging field of targeting the DC-T cell interaction for antigen-specific immunotherapy of RA.
树突状细胞(DCs)是连接先天免疫和适应性免疫反应的关键专业抗原呈递细胞,诱导初始 CD4 T 细胞向效应细胞的启动和分化、CD8 T 细胞的交叉启动以及 B 细胞抗体反应的促进。DCs 在维持免疫稳态和耐受方面也起着关键作用。DC-T 细胞相互作用是类风湿关节炎(RA)中自身免疫反应产生的基础。在这里,我们描述了 DCs 的功能,并回顾了 DCs 和 T 细胞在 RA 发病机制中的作用的证据,特别是通过 DCs 呈递自身肽来触发自身反应性 T 细胞的分化和激活。最后,我们讨论了针对 DC-T 细胞相互作用的新兴领域,以实现 RA 的抗原特异性免疫治疗。