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Targeting interleukin-6 in inflammatory autoimmune diseases and cancers

Authors :
Michael Fung
Yihong Yao
Nan Shen
Jiaqi Huang
Xin Yao
Haihong Zhong
Raffaella Faggioni
Source :
Pharmacology & Therapeutics. 141:125-139
Publication Year :
2014
Publisher :
Elsevier BV, 2014.

Abstract

Interleukin-6 (IL-6) is a pleiotropic cytokine with significant functions in the regulation of the immune system. As a potent pro-inflammatory cytokine, IL-6 plays a pivotal role in host defense against pathogens and acute stress. However, increased or deregulated expression of IL-6 significantly contributes to the pathogenesis of various human diseases. Numerous preclinical and clinical studies have revealed the pathological roles of the IL-6 pathway in inflammation, autoimmunity, and cancer. Based on the rich body of studies on biological activities of IL-6 and its pathological roles, therapeutic strategies targeting the IL-6 pathway are in development for cancers, inflammatory and autoimmune diseases. Several anti-IL-6/IL-6 receptor monoclonal antibodies developed for targeted therapy have demonstrated promising results in both preclinical studies and clinical trials. Tocilizumab, an anti-IL-6 receptor antibody, is effective in the treatment of various autoimmune and inflammatory conditions notably rheumatoid arthritis. It is the only IL-6 pathway targeting agent approved by the regulatory agencies for clinical use. Siltuximab, an anti-IL-6 antibody, has been shown to have potential benefits treating various human cancers either as a single agent or in combination with other chemotherapy drugs. Several other anti-IL-6-based therapies are also under clinical development for various diseases. IL-6 antagonism has been shown to be a potential therapy for these disorders refractory to conventional drugs. New strategies, such as combination of IL-6 blockade with inhibition of other signaling pathways, may further improve IL-6-targeted immunotherapy of human diseases.

Details

ISSN :
01637258
Volume :
141
Database :
OpenAIRE
Journal :
Pharmacology & Therapeutics
Accession number :
edsair.doi.dedup.....11cddecdfa69639aa5cb076b2b14f132
Full Text :
https://doi.org/10.1016/j.pharmthera.2013.09.004