| Literature DB >> 31578241 |
Eric M Tam1, Ross B Fulton2, James F Sampson2, Marco Muda2, Adam Camblin2, Jennifer Richards2, Alexander Koshkaryev2, Jian Tang2, Vinodh Kurella2, Yang Jiao2, Lihui Xu2, Kathy Zhang2, Neeraj Kohli2, Lia Luus2, Elizabeth Hutto3, Sandeep Kumar2, James Lulo2, Violette Paragas2, Christina Wong2, James Suchy2, Stephanie Grabow2, Anne-Sophie Dugast2, Hong Zhang2, Fabien Depis2, Sonia Feau2, Aniela Jakubowski2, Wenlian Qiao2, Galina Craig2, Maja Razlog2, James Qiu2, Yu Zhou4, James D Marks4, Michael Croft5,6, Daryl C Drummond2, Andreas Raue1.
Abstract
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.Entities:
Year: 2019 PMID: 31578241 DOI: 10.1126/scitranslmed.aax0720
Source DB: PubMed Journal: Sci Transl Med ISSN: 1946-6234 Impact factor: 17.956