嵌合抗原受体
黑色素瘤
免疫疗法
T细胞受体
过继性细胞移植
医学
细胞疗法
免疫学
T细胞
抗原
癌症研究
癌症免疫疗法
细胞
免疫系统
生物
遗传学
作者
Efrat Merhavi-Shoham,Orit Itzhaki,Gal Markel,Jacob Schachter,Michal J. Besser
出处
期刊:The cancer journal
[Lippincott Williams & Wilkins]
日期:2017-01-01
卷期号:23 (1): 48-53
被引量:60
标识
DOI:10.1097/ppo.0000000000000240
摘要
Adoptive cell therapy (ACT) of tumor-infiltrating lymphocytes (TILs) is a powerful form of immunotherapy by inducing durable complete responses that significantly extend the survival of melanoma patients. Mutation-derived neoantigens were recently identified as key factors for tumor recognition and rejection by TILs. The isolation of T-cell receptor (TCR) genes directed against neoantigens and their retransduction into peripheral T cells may provide a new form of ACT.Genetic modifications of T cells with chimeric antigen receptors (CARs) have demonstrated remarkable clinical results in hematologic malignancies, but are so far less effective in solid tumors. Only very limited reports exist in melanoma. Progress in CAR T-cell engineering, including neutralization of inhibitory signals or additional safety switches, may open opportunities also in melanoma.We review clinical results and latest developments of adoptive therapies with TILs, T-cell receptor, and CAR-modified T cells and discuss future directions for the treatment of melanoma.
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