免疫
抗体
细胞毒性T细胞
免疫系统
癌症研究
CD8型
免疫学
医学
生物
化学
体外
生物化学
作者
Eric M. Tam,Ross B. Fulton,James F. Sampson,Marco Muda,Adam J. Camblin,Jennifer Richards,Alexander Koshkaryev,Jian Tang,Vinodh B. Kurella,Yang Jiao,Lihui Xu,Kathy Zhang,Neeraj Kohli,Lia Luus,Elizabeth Hutto,Sandeep Kumar,James Lulo,Violette Paragas,Christina S.F. Wong,James Suchy
标识
DOI:10.1126/scitranslmed.aax0720
摘要
Tumor necrosis factor receptor 2 (TNFR2) is the alternate receptor for TNF and can mediate both pro- and anti-inflammatory activities of T cells. Although TNFR2 has been linked to enhanced suppressive activity of regulatory T cells (Tregs) in autoimmune diseases, the viability of TNFR2 as a target for cancer immunotherapy has been underappreciated. Here, we show that new murine monoclonal anti-TNFR2 antibodies yield robust antitumor activity and durable protective memory in multiple mouse cancer cell line models. The antibodies mediate potent Fc-dependent T cell costimulation and do not result in significant depletion of Tregs Corresponding human agonistic monoclonal anti-TNFR2 antibodies were identified and also had antitumor effects in humanized mouse models. Anti-TNFR2 antibodies could be developed as a novel treatment option for patients with cancer.
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