Sorbonne Université, INSERM, CNRS, Centre d'Immunologie et des Maladies Infectieuses (CIMI-Paris), Paris, France.
Nat Rev Rheumatol. 2021 Aug;17(8):487-504. doi: 10.1038/s41584-021-00639-6. Epub 2021 Jul 5.
Treatments that block tumour necrosis factor (TNF) have major beneficial effects in several autoimmune and rheumatic diseases, including rheumatoid arthritis. However, some patients do not respond to TNF inhibitor treatment and rare occurrences of paradoxical disease exacerbation have been reported. These limitations on the clinical efficacy of TNF inhibitors can be explained by the differences between TNF receptor 1 (TNFR1) and TNFR2 signalling and by the diverse effects of TNF on multiple immune cells, including FOXP3 regulatory T cells. This basic knowledge sheds light on the consequences of TNF inhibitor therapies on regulatory T cells in treated patients and on the limitations of such treatment in the control of diseases with an autoimmune component. Accordingly, the next generation of drugs targeting TNF is likely to be based on agents that selectively block the binding of TNF to TNFR1 and on TNFR2 agonists. These approaches could improve the treatment of rheumatic diseases in the future.
阻断肿瘤坏死因子 (TNF) 的治疗方法对包括类风湿关节炎在内的几种自身免疫性和风湿性疾病具有重要的有益效果。然而,一些患者对 TNF 抑制剂治疗没有反应,并且已经报道了罕见的矛盾疾病恶化病例。TNF 抑制剂在临床疗效上的这些局限性可以通过 TNF 受体 1 (TNFR1) 和 TNFR2 信号转导之间的差异以及 TNF 对包括 FOXP3 调节性 T 细胞在内的多种免疫细胞的多种作用来解释。这些基础知识阐明了 TNF 抑制剂治疗对接受治疗患者的调节性 T 细胞的影响,以及这种治疗在控制具有自身免疫成分的疾病方面的局限性。因此,靶向 TNF 的下一代药物可能基于选择性阻断 TNF 与 TNFR1 结合的药物和 TNFR2 激动剂。这些方法可能会改善未来风湿性疾病的治疗效果。