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Review article

Evolving Roles for Targeting CTLA-4 in Cancer Immunotherapy

Yinghao ZhaoJilin Provincial Key Laboratory on Molecular and Chemical Genetic, the Second Hospital of Jilin University, Changchun, ChinaWei YangJilin Provincial Key Laboratory on Molecular and Chemical Genetic, the Second Hospital of Jilin University, Changchun, ChinaYuanyuan HuangDepartment of pediatric, the First Hospital of Jilin University, Changchun, ChinaRanji CuiJilin Provincial Key Laboratory on Molecular and Chemical Genetic, the Second Hospital of Jilin University, Changchun, ChinaXiangyan LiJilin Provincial Key Laboratory of BioMacromolecules of Chinese Medicine, Jilin Ginseng Academy, Changchun University of Chinese Medicine, The Affiliated Hospital to Changchun University of Chinese Medicine, Changchun, ChinaBingjin LiJilin Provincial Key Laboratory on Molecular and Chemical Genetic, the Second Hospital of Jilin University, Changchun, China
2018en
ABI

Abstract

Cytotoxic T lymphocyte-associated antigen-4 (CTLA-4) is a membrane glycoprotein expressed by activated effector T cells (Teffs) and participates in the repression of T cell proliferation, cell cycle progression and cytokine production. Currently, antibodies targeting CTLA-4, ipilimumab and tremelimumab are widely used as a therapeutic approach in a variety of human malignancies. However, their detailed mechanism remains unclear. Therefore, in this review, we focused specifically on recent findings concerning the role of CTLA-4 in immune response and also discussed clinical studies of targeting CTLA-4, alone or in combination with other therapies for the treatment of cancers. CTLA-4 blockade is used as a therapeutic approach for the treatment of cancer through competing with CD28-positive costimulation for binding to their shared B7 ligands or exhibiting direct inhibitory effect on signaling molecules in the cytoplasmic tail. At present, antibodies for targeting CTLA-4 or in combination with other therapies significantly reinforced the anti-tumor effect and improved the prognosis of malignant disease. In addition, severe adverse events of targeting CTLA-4 therapy could be a challenge for the development of this therapeutic strategy. This review may provide some new insights for clinical studies of targeting CTLA-4.

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