The Biology and Medical Implications of Interleukin-6

被引:292
作者
Tanaka, Toshio [1 ]
Kishimoto, Tadamitsu [2 ]
机构
[1] Osaka Univ, Grad Sch Med, Dept Clin Applicat Biol, Suita, Osaka 5650871, Japan
[2] Osaka Univ, World Premier Int Immunol Frontier Res Ctr, Lab Immune Regulat, Suita, Osaka 5650871, Japan
关键词
ANTI-INTERLEUKIN-6 RECEPTOR ANTIBODY; TOCILIZUMAB MONOTHERAPY; DOUBLE-BLIND; ARTHRITIS; EXPRESSION; STABILITY; CLONING; TRIAL;
D O I
10.1158/2326-6066.CIR-14-0022
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Cytokines are soluble mediators, which aid cell-to-cell communication in immune responses, and interleukin-6 (IL-6) is a prototypical cytokine featuring redundant and pleiotropic activity. The complete elucidation of the IL6-mediated signal transduction system has provided a molecular basis for the characteristic features of cytokines. When tissue damage or inflammation due to infections or injuries occurs, IL-6 synthesis is promptly induced, contributing to the host defense through the stimulation of acute-phase immune reactions and hematopoiesis. The production of IL-6 is terminated when tissue homeostasis is restored. The synthesis of IL-6 is tightly regulated transcriptionally and posttranscriptionally. However, the dysregulated continual synthesis of IL-6 has been implicated in the development of various diseases, including autoimmune and chronic inflammatory diseases and cancers. Clinical trials using the humanized anti-IL-6 receptor monoclonal antibody tocilizumab have demonstrated the efficacy of IL-6 blockade for the treatment of refractory inflammatory diseases, such as rheumatoid arthritis, systemic juvenile idiopathic arthritis, and Castleman disease. Moreover, favorable results from the off-label use of tocilizumab strongly suggest that it may be applicable for the treatment of other refractory immune-mediated diseases, including cancer. Therefore, the mechanisms for the dysregulated synthesis of IL-6 need to be elucidated to understand the pathogenesis of the resultant diseases and to facilitate the development of effective therapeutic strategies. (C)2014 AACR.
引用
收藏
页码:288 / 294
页数:7
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