Guedan Sonia, Calderon Hugo, Posey Avery D, Maus Marcela V
Department of Hematology, Hospital Clinic, Institut d'Investigacions Biomèdiques August Pi i Sunyer (IDIBAPS), 08036 Barcelona, Spain.
Center for Cellular Immunotherapies, Perelman School of Medicine at the University of Pennsylvania, Philadelphia, PA, USA.
Mol Ther Methods Clin Dev. 2018 Dec 31;12:145-156. doi: 10.1016/j.omtm.2018.12.009. eCollection 2019 Mar 15.
T cells engineered with chimeric antigen receptors (CARs) have emerged as a potent new class of therapeutics for cancer, based on their remarkable potency in blood cancers. Since the first clinical reports of their efficacy emerged 7 years ago, investigators have focused on the mechanisms and properties that make CARs effective or toxic, and their effects on T cell biology. Novel CAR designs coupled with improvements in gene transfer technology, incorporating advances in gene editing, have the potential to increase access to engineered cell therapies, as well as improve their potency in solid tumors.
嵌合抗原受体(CAR)工程化的T细胞已成为一类有效的新型癌症治疗药物,这基于它们在血癌中显著的效力。自7年前首次有关于其疗效的临床报告出现以来,研究人员一直专注于使CAR发挥作用或产生毒性的机制和特性,以及它们对T细胞生物学的影响。结合基因编辑进展的新型CAR设计与基因转移技术的改进,有可能增加工程细胞疗法的可及性,并提高它们在实体瘤中的效力。