嵌合抗原受体
CD19
实体瘤
免疫疗法
抗原
医学
T细胞
肿瘤微环境
癌症研究
免疫学
癌症免疫疗法
肿瘤细胞
细胞疗法
细胞
生物
癌症
免疫系统
内科学
遗传学
作者
Kheng Newick,Shaun O’Brien,Edmund K. Moon,Steven Μ. Albelda
标识
DOI:10.1146/annurev-med-062315-120245
摘要
The field of cancer immunotherapy has been re-energized by the application of chimeric antigen receptor (CAR) T cell therapy in cancers. These CAR T cells are engineered to express synthetic receptors that redirect polyclonal T cells to surface antigens for subsequent tumor elimination. Many CARs are designed with elements that augment T cell persistence and activity. To date, CAR T cells have demonstrated tremendous success in eradicating hematologic malignancies (e.g., CD19 CARs in leukemias). However, this success has yet to be extrapolated to solid tumors, and the reasons for this are being actively investigated. We characterize some of the challenges that CAR T cells have to surmount in the solid tumor microenvironment and new approaches that are being considered to overcome these hurdles.
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