Thomas Ranjeny
Arthritis Res Ther. 2013 Feb 4;15(1):204. doi: 10.1186/ar4130.
Rheumatoid arthritis (RA) is a systemic inflammatory disease resulting from an autoimmune response to self-antigens, leading to inflammation of synovial tissue of joints and subsequent cartilage and bone erosion. Current disease-modifying anti-rheumatic drugs and biologic inhibitors of TNF, IL-6, T cells and B cells block inflammation nonspecifically, which may lead to adverse effects, including infection. They do not generally induce long-term drug-free remission or restoration of immune tolerance to self-antigens, and lifelong treatment is usual. The development of antigen-specific strategies in RA has so far been limited by insufficient knowledge of autoantigens, of the autoimmune pathogenesis of RA and of the mechanisms of immune tolerance in man. Effective tolerance-inducing antigen-specific immunotherapeutic strategies hold promise of greater specificity, of lower toxicity and of a longer-term solution for controlling or even preventing RA. This paper reviews current understanding of autoantigens and their relationship to immunopathogenesis of RA, and emerging therapeutics that aim to leverage normal tolerance mechanisms for implementation of antigen-specific therapy in RA.
类风湿关节炎(RA)是一种全身性炎症性疾病,由针对自身抗原的自身免疫反应引起,导致关节滑膜组织炎症以及随后的软骨和骨侵蚀。目前的改善病情抗风湿药物以及肿瘤坏死因子、白细胞介素-6、T细胞和B细胞的生物抑制剂会非特异性地阻断炎症,这可能会导致包括感染在内的不良反应。它们通常不会诱导长期的无药缓解或恢复对自身抗原的免疫耐受,通常需要终身治疗。迄今为止,RA中抗原特异性策略的发展受到对自身抗原、RA自身免疫发病机制以及人类免疫耐受机制了解不足的限制。有效的诱导耐受的抗原特异性免疫治疗策略有望具有更高的特异性、更低的毒性,并为控制甚至预防RA提供更长期的解决方案。本文综述了目前对自身抗原及其与RA免疫发病机制关系的理解,以及旨在利用正常耐受机制在RA中实施抗原特异性治疗的新兴疗法。