IL-6 Revisited: From Rheumatoid Arthritis to CAR T Cell Therapy and COVID-19

被引:84
作者
Kishimoto, Tadamitsu [1 ]
Kang, Sujin [1 ]
机构
[1] Osaka Univ, WPI Immunol Frontier Res Ctr, Lab Immune Regulat, Osaka, Japan
关键词
interleukin-6; IL-6R; tocilizumab; rheumatoid arthritis; cytokine storms; COVID-19; CYTOKINE-RELEASE SYNDROME; ANTI-INTERLEUKIN-6 RECEPTOR ANTIBODY; JUVENILE IDIOPATHIC ARTHRITIS; ARYL-HYDROCARBON RECEPTOR; NF-KAPPA-B; DOUBLE-BLIND; IN-VITRO; NEUROMYELITIS-OPTICA; INTERLEUKIN-6; GENE; ENDOTHELIAL ACTIVATION;
D O I
10.1146/annurev-immunol-101220-023458
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The diverse biological activity of interleukin-6 (IL-6) contributes to the maintenance of homeostasis. Emergent infection or tissue injury induces rapid production of IL-6 and activates host defense through augmentation of acute-phase proteins and immune responses. However, excessive IL-6 production and uncontrolled IL-6 receptor signaling are critical to pathogenesis. Over the years, therapeutic agents targeting IL-6 signaling, such as tocilizumab, a humanized anti-IL-6 receptor antibody, have shown remarkable efficacy for rheumatoid arthritis, Castleman disease, and juvenile idiopathic arthritis, and their efficacy in other diseases is continually being reported. Emerging evidence has demonstrated the benefit of tocilizumab for several types of acute inflammatory diseases, including cytokine storms induced by chimeric antigen receptor T cell therapy and coronavirus disease 2019 (COVID-19). Here, we refocus attention on the biology of IL-6 and summarize the distinct pathological roles of IL-6 signaling in several acute and chronic inflammatory diseases.
引用
收藏
页码:323 / 348
页数:26
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