医学
嵌合抗原受体
前列腺癌
雄激素剥夺疗法
放射治疗
肿瘤科
细胞疗法
T细胞
内科学
癌症研究
化疗
靶向治疗
细胞
免疫疗法
癌症
免疫学
免疫系统
生物
遗传学
作者
Philipp Wolf,Jamal Alzubi,Christian Gratzke,Toni Cathomen
标识
DOI:10.1038/s41585-021-00488-8
摘要
Chimeric antigen receptor (CAR) T cell immunotherapy involves the genetic modification of the patient’s own T cells so that they specifically recognize and destroy tumour cells. Considerable clinical success has been achieved using this technique in patients with lymphoid malignancies, but clinical studies that investigated treating solid tumours using this emerging technology have been disappointing. A number of developments might be able to increase the efficacy of CAR T cell therapy for treatment of prostate cancer, including improved trafficking to the tumour, techniques to overcome the immunosuppressive tumour microenvironment, as well as methods to enhance CAR T cell persistence, specificity and safety. Furthermore, CAR T cell therapy has the potential to be combined with other treatment modalities, such as androgen deprivation therapy, radiotherapy or chemotherapy, and could be applied as focal CAR T cell therapy for prostate cancer.
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