免疫系统
癌症
免疫疗法
免疫学
单克隆抗体
易普利姆玛
黑色素瘤
癌症免疫疗法
附带损害
癌症研究
细胞毒性T细胞
靶向治疗
临床试验
医学
生物
抗体
生物信息学
体外
心理学
内科学
犯罪学
生物化学
作者
Simone Mocellin,Clara Benna,Pierluigi Pilati
标识
DOI:10.1016/j.cytogfr.2013.01.003
摘要
The adaptive immune response is controlled by checkpoints represented by coinhibitory molecules, which are crucial for maintaining self-tolerance and minimizing collateral tissue damage under physiological conditions. A growing body of preclinical evidence supports the hypothesis that unleashing this immunological break might be therapeutically beneficial in the fight against cancer, as it would elicit an effective antitumor immune response. Remarkably, recent clinical trials have demonstrated that this novel strategy can be highly effective in the treatment of patients with cancer, as shown by the paradigmatic case of ipilimumab (a monoclonal antibody blocking the coinhibitory molecule cytotoxic T lymphocyte associated antigen-4 [CTLA4]) that is opening a new era in the therapeutic approach to a chemoresistant tumor such as cutaneous melanoma. In this review we summarize the biology of coinhibitory molecules, overview the experimental and clinical attempts to interfere with these immune checkpoints to treat cancer and critically discuss the challenges posed by such a promising antitumor modality.
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