CAR T-cells for cancer therapy

被引:34
|
作者
Muhammad, Niaz [1 ]
Mao, Qinwen [2 ]
Xia, Haibin [1 ]
机构
[1] Shaanxi Normal Univ, Dept Biochem, Coll Life Sci, Lab Gene Therapy, Xian, Shaanxi, Peoples R China
[2] Northwestern Univ, Dept Pathol, Feinberg Sch Med, Chicago, IL 60611 USA
基金
中国国家自然科学基金;
关键词
Chimeric antigen receptor; immunotherapy; T-cell; cancer; single-chain variable fragment; CHIMERIC-ANTIGEN-RECEPTOR; ACUTE LYMPHOBLASTIC-LEUKEMIA; IN-VIVO PERSISTENCE; ANTITUMOR-ACTIVITY; SUICIDE-GENE; ADOPTIVE IMMUNOTHERAPY; SIGNAL-TRANSDUCTION; DONOR LYMPHOCYTES; PHASE-I; EFFECTOR FUNCTIONS;
D O I
10.1080/02648725.2018.1430465
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Chimeric antigen receptor (CAR) T-cells are redirected T-cells that can recognize cancer antigens in a major histocompatibility complex (MHC)-independent fashion. A typical CAR is comprised of two main functional domains: an extracellular antigen recognition domain, called a single-chain variable fragment (scFv), and an intracellular signaling domain. Based on the number of intracellular signaling molecules, CARs are categorized into four generations. CAR T-cell therapy has become a promising treatment for hematologic malignancies. However, results of its clinical trials on solid tumors have not been encouraging. Here, we described the structure of CARs and summarized the clinical trials of CD19-targeted CAR T-cells. The side effects, safety management, challenges, and future prospects of CAR T-cells for the treatment of cancer, particularly for solid tumors, were also discussed.
引用
收藏
页码:190 / 226
页数:37
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