Antibody-mediated targeting of TNFR2 activates CD8+ T cells in mice and promotes antitumor immunity.
Eric M TamRoss B FultonJames F SampsonMarco MudaAdam CamblinJennifer RichardsAlexander KoshkaryevJian TangVinodh KurellaYang JiaoLihui XuKathy ZhangNeeraj KohliLia LuusElizabeth HuttoSandeep KumarJames LuloViolette ParagasChristina S F WongJames J SuchyStephanie GrabowAnne-Sophie DugastHong ZhangFabien DepisSonia FeauAniela JakubowskiWenlian QiaoGalina CraigMaja RazlogJames QiuYu ZhouJames D MarksMichael CroftDaryl C DrummondAndreas RauePublished in: Science translational medicine (2020)
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.