TY - JOUR
T1 - Translating IL-6 biology into effective treatments
AU - Choy, Ernest H.
AU - De Benedetti, Fabrizio
AU - Takeuchi, Tsutomu
AU - Hashizume, Misato
AU - John, Markus R.
AU - Kishimoto, Tadamitsu
N1 - Funding Information:
E.H.C. has received research grants from Bio-Cancer, Biogen, Novartis, Pfizer, Roche, Sanofi and UCB; consultancy fees from AbbVie, Amgen, Biogen, Chugai Pharma, Eli Lilly, Janssen, Novartis, Pfizer, Regeneron, Roche, R-Pharm and Sanofi; speaker’s fees from Amgen, Bristol-Myers Squibb, Chugai Pharma, Eli Lilly, Janssen, Novartis, Pfizer, Regeneron, Roche, Sanofi and UCB. F.D.B. has received research grants from AbbVie, Novartis, Pfizer, Roche, Sanofi, Novimmune and SOBI. T.T. has received research grants from AbbVie, Asahi Kasei Pharma, Astellas Pharma, AYUMI Pharmaceutical, Chugai Pharmaceutical, Daiichi Sankyo, Eisai, Mitsubishi Tanabe Pharma, Nippon Kayaku, Novartis Pharma K.K., Pfizer Japan, Takeda Pharmaceutical; and personal fees from AbbVie G.K., Astellas Pharma, AstraZeneca K.K., Bristol-Myers K.K., Chugai Pharmaceutical, Daiichi Sankyo, Eisai, Eli Lilly Japan K.K., GlaxoSmithKline K.K., Janssen Pharmaceutical K.K., Mitsubishi Tanabe Pharma, Nippon Kayaku, Novartis Pharma K.K., Pfizer Japan, Sanofi K.K., Teijin Pharma, Taiho Pharmaceutical, Taisho Pharmaceutical, Takeda Pharmaceutical, UCB Japan. M.H. is an employee of Chugai Pharmaceutical. M.R.J. is employed by Roche and owns shares in Roche. T.K. has a patent for tocilizumab. Work by T.K.’s group is supported in part by the Kishimoto Foundation.
Publisher Copyright:
© 2020, Springer Nature Limited.
PY - 2020/6/1
Y1 - 2020/6/1
N2 - In 1973, IL-6 was identified as a soluble factor that is secreted by T cells and is important for antibody production by B cells. Since its discovery more than 40 years ago, the IL-6 pathway has emerged as a pivotal pathway involved in immune regulation in health and dysregulation in many diseases. Targeting of the IL-6 pathway has led to innovative therapeutic approaches for various rheumatic diseases, such as rheumatoid arthritis, juvenile idiopathic arthritis, adult-onset Still’s disease, giant cell arteritis and Takayasu arteritis, as well as other conditions such as Castleman disease and cytokine release syndrome. Targeting this pathway has also identified avenues for potential expansion into several other indications, such as uveitis, neuromyelitis optica and, most recently, COVID-19 pneumonia. To mark the tenth anniversary of anti-IL-6 receptor therapy worldwide, we discuss the history of research into IL-6 biology and the development of therapies that target IL-6 signalling, including the successes and challenges and with an emphasis on rheumatic diseases.
AB - In 1973, IL-6 was identified as a soluble factor that is secreted by T cells and is important for antibody production by B cells. Since its discovery more than 40 years ago, the IL-6 pathway has emerged as a pivotal pathway involved in immune regulation in health and dysregulation in many diseases. Targeting of the IL-6 pathway has led to innovative therapeutic approaches for various rheumatic diseases, such as rheumatoid arthritis, juvenile idiopathic arthritis, adult-onset Still’s disease, giant cell arteritis and Takayasu arteritis, as well as other conditions such as Castleman disease and cytokine release syndrome. Targeting this pathway has also identified avenues for potential expansion into several other indications, such as uveitis, neuromyelitis optica and, most recently, COVID-19 pneumonia. To mark the tenth anniversary of anti-IL-6 receptor therapy worldwide, we discuss the history of research into IL-6 biology and the development of therapies that target IL-6 signalling, including the successes and challenges and with an emphasis on rheumatic diseases.
UR - http://www.scopus.com/inward/record.url?scp=85083979238&partnerID=8YFLogxK
UR - http://www.scopus.com/inward/citedby.url?scp=85083979238&partnerID=8YFLogxK
U2 - 10.1038/s41584-020-0419-z
DO - 10.1038/s41584-020-0419-z
M3 - Comment/debate
C2 - 32327746
AN - SCOPUS:85083979238
SN - 1759-4790
VL - 16
SP - 335
EP - 345
JO - Nature Reviews Rheumatology
JF - Nature Reviews Rheumatology
IS - 6
ER -