Abstract |
Patients with malignant tumor treated with immunotherapy have received significant clinical benefits over the years. Immune checkpoint blocking agents, such as anti-cytotoxic T-lymphocyte-associated protein-4 (anti-CTLA-4) and anti-programmed cell death protein-1 (anti-PD-1) monoclonal antibodies, have produced impressive clinical results in different types of cancer. T-cell immunoglobulin and mucin domain-3 (TIM-3), another immune checkpoint, could inhibit cancer immunity. Recent studies have highlighted that TIM-3 has an important role to play in T-cell exhaustion and correlates with the outcome of anti-PD-1 therapy. Targeting TIM-3 might be a promising approach for cancer immunotherapy. Here, we review the role of TIM-3 in cancer and clinical trials with TIM-3 inhibitors.
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Authors | Yayi He, Jie Cao, Chao Zhao, Xuefei Li, Caicun Zhou, Fred R Hirsch |
Journal | OncoTargets and therapy
(Onco Targets Ther)
Vol. 11
Pg. 7005-7009
( 2018)
ISSN: 1178-6930 [Print] New Zealand |
PMID | 30410357
(Publication Type: Journal Article, Review)
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