Boosting cancer immunotherapy with anti-CD137 antibody therapy

A Yonezawa, S Dutt, C Chester, J Kim, HE Kohrt - Clinical Cancer Research, 2015 - AACR
A Yonezawa, S Dutt, C Chester, J Kim, HE Kohrt
Clinical Cancer Research, 2015AACR
In the past 5 years, immunomodulatory antibodies have revolutionized cancer
immunotherapy. CD137, a member of the tumor necrosis factor receptor superfamily,
represents a promising target for enhancing antitumor immune responses. CD137 helps
regulate the activation of many immune cells, including CD4+ T cells, CD8+ T cells, dendritic
cells, and natural killer cells. Recent studies indicate that the antitumor efficacy of
therapeutic tumor-targeting antibodies can be augmented by the addition of agonistic …
Abstract
In the past 5 years, immunomodulatory antibodies have revolutionized cancer immunotherapy. CD137, a member of the tumor necrosis factor receptor superfamily, represents a promising target for enhancing antitumor immune responses. CD137 helps regulate the activation of many immune cells, including CD4+ T cells, CD8+ T cells, dendritic cells, and natural killer cells. Recent studies indicate that the antitumor efficacy of therapeutic tumor-targeting antibodies can be augmented by the addition of agonistic antibodies targeting CD137. As ligation of CD137 provides a costimulatory signal in multiple immune cell subsets, combination therapy of CD137 antibody with therapeutic antibodies and/or vaccination has the potential to improve cancer treatment. Recently, clinical trials of combination therapies with agonistic anti-CD137 mAbs have been launched. In this review, we discuss the recent advances and clinical promise of agonistic anti-CD137 monoclonal antibody therapy. Clin Cancer Res; 21(14); 3113–20. ©2015 AACR.
AACR