4.5 Review

TIM-3, a promising target for cancer immunotherapy

Journal

ONCOTARGETS AND THERAPY
Volume 11, Issue -, Pages 7005-7009

Publisher

DOVE MEDICAL PRESS LTD
DOI: 10.2147/OTT.S170385

Keywords

immune checkpoint; clinical trial; cancer immunotherapy; T-cell immunoglobulin and mucin domain-3 (TIM-3)

Funding

  1. National Natural Science Foundation of China [81802255]
  2. Shanghai Pujiang Program [17PJD036]
  3. Shanghai Municipal Commission of Health and Family Planning Program [20174Y0131]
  4. National key research & development project [2016YFC0902300]
  5. Major disease clinical skills enhancement program of three year action plan for promoting clinical skills and clinical innovation in municipal hospitals
  6. Shanghai Shen Kang Hospital Development Center Clinical Research Plan of SHDC [16CR1001A]
  7. fundamental research funds for the central universities

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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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