类风湿性关节炎
医学
肿瘤坏死因子α
促炎细胞因子
细胞因子
免疫学
调解人
关节炎
药理学
炎症
内科学
作者
Alexander Vugler,James P. O’Connell,Mai Ánh Nguyễn,Dietmar Weitz,Thomas Leeuw,Elizabeth S. Hickford,Alexander Verbitsky,Xiaoyou Ying,Markus Rehberg,Bruce Carrington,Mark Merriman,Andrew Moss,Jean-Marie Nicholas,Phil Stanley,S. Kirk Wright,Tim Bourne,Yann Foricher,Daniel C. Brookings,Helen Horsley,Matthias Herrmann,Srinivas Rao,Markus Kohlmann,Peter Florian
标识
DOI:10.3389/fphar.2022.1037983
摘要
Tumor necrosis factor (TNF) is a pleiotropic cytokine belonging to a family of trimeric proteins with both proinflammatory and immunoregulatory functions. TNF is a key mediator in autoimmune diseases and during the last couple of decades several biologic drugs have delivered new therapeutic options for patients suffering from chronic autoimmune diseases such as rheumatoid arthritis and chronic inflammatory bowel disease. Attempts to design small molecule therapies directed to this cytokine have not led to approved products yet. Here we report the discovery and development of a potent small molecule inhibitor of TNF that was recently moved into phase 1 clinical trials. The molecule, SAR441566, stabilizes an asymmetrical form of the soluble TNF trimer, compromises downstream signaling and inhibits the functions of TNF in vitro and in vivo. With SAR441566 being studied in healthy volunteers we hope to deliver a more convenient orally bioavailable and effective treatment option for patients suffering with chronic autoimmune diseases compared to established biologic drugs targeting TNF.
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