Kang Sujin, Tanaka Toshio, Kishimoto Tadamitsu
Department of Clinical Application of Biologics, Osaka University Graduate School of Medicine, 2-2 Yamada-oka, Suita City, Osaka 565-0871, Japan Department of Immunopathology, World Premier International Immunology Frontier Research Center, Osaka University, 3-1 Yamada-oka, Suita City, Osaka 565-0871, Japan.
Laboratory of Immune Regulation, World Premier International Immunology Frontier Research Center, Osaka University, 3-1 Yamada-oka, Suita City, Osaka 565-0871, Japan
Int Immunol. 2015 Jan;27(1):21-9. doi: 10.1093/intimm/dxu081. Epub 2014 Aug 20.
Cytokine-targeted therapy has generated a paradigm shift in the treatment of several immune-mediated diseases. Interleukin-6 (IL-6), which was initially identified as B-cell stimulatory factor 2, is a prototypical cytokine with wide-ranging biological effects on immune cells such as B and T cells, on hepatocytes, hematopoietic cells, vascular endothelial cells and on many others. IL-6 is thus crucially involved in the regulation of immune responses, hematopoiesis and inflammation. When infections and tissue injuries occur, IL-6 is promptly synthesized and performs a protective role in host defense against such stresses and traumas. However, excessive production of IL-6 during this emergent process induces potentially fatal complications, including systemic inflammatory response syndrome (SIRS), and dysregulated, persistently high expression of IL-6 causes the onset or development of various chronic immune-mediated disorders. For these reasons, IL-6 blockade was expected to become a novel therapeutic strategy for various diseases characterized by IL-6 overproduction. Indeed, worldwide clinical trials of tocilizumab, a humanized anti-IL-6 receptor monoclonal antibody, have successfully proved its outstanding efficacy against rheumatoid arthritis, juvenile idiopathic arthritis and Castleman disease, leading to the approval of tocilizumab for the treatment of these diseases. Moreover, various reports regarding off-label use of tocilizumab strongly suggest that it will be widely applicable for acute, severe complications such as SIRS and cytokine-release syndrome and other refractory chronic immune-mediated diseases.
细胞因子靶向治疗已在多种免疫介导疾病的治疗中引发了范式转变。白细胞介素-6(IL-6)最初被鉴定为B细胞刺激因子2,是一种典型的细胞因子,对免疫细胞(如B细胞和T细胞)、肝细胞、造血细胞、血管内皮细胞等许多细胞具有广泛的生物学效应。因此,IL-6在免疫反应、造血和炎症的调节中起着至关重要的作用。当发生感染和组织损伤时,IL-6会迅速合成,并在宿主抵御此类应激和创伤中发挥保护作用。然而,在此紧急过程中IL-6的过度产生会引发潜在致命并发症,包括全身炎症反应综合征(SIRS),并且IL-6失调、持续高表达会导致各种慢性免疫介导疾病的发生或发展。基于这些原因,IL-6阻断有望成为针对以IL-6过度产生为特征的各种疾病的新型治疗策略。事实上,人源化抗IL-6受体单克隆抗体托珠单抗的全球临床试验已成功证明其对类风湿性关节炎、幼年特发性关节炎和Castleman病具有出色疗效,从而使托珠单抗获批用于治疗这些疾病。此外,关于托珠单抗超说明书用药的各种报告强烈表明,它将广泛适用于SIRS和细胞因子释放综合征等急性、严重并发症以及其他难治性慢性免疫介导疾病。