Challenges and prospects of chimeric antigen receptor T cell therapy in solid tumors

被引:28
|
作者
Jindal, Vishal [1 ]
Arora, Ena [2 ]
Gupta, Sorab [3 ]
机构
[1] St Vincent Hosp, Dept Internal Med, 123 Summer St, Worcester, MA 01608 USA
[2] Govt Med Coll, Dept Internal Med, Chandigarh, India
[3] Einstein Healthcare Network, Dept Hematol & Oncol, Philadelphia, PA USA
关键词
Chimeric antigen receptor T cell therapy; Solid tumors; Immunotherapy; FIBROBLAST ACTIVATION PROTEIN; GROWTH-FACTOR-RECEPTOR; INDOLEAMINE 2,3-DIOXYGENASE; ANTITUMOR-ACTIVITY; PHASE-I; ADOPTIVE IMMUNOTHERAPY; STROMAL FIBROBLASTS; ESTABLISHED TUMORS; OXIDATIVE STRESS; LYMPHOCYTES;
D O I
10.1007/s12032-018-1149-9
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
Chimeric antigen receptor (CAR) T cell therapy is a novel and innovative immunotherapy. CAR-T cells are genetically engineered T cells, carrying MHC independent specific antigen receptor and co-stimulatory molecule which can activate an immune response to a cancer specific antigen. This therapy showed great results in hematological malignancies but were unable to prove their worth in solid tumors. Likely reasons for their failure are lack of antigens, poor trafficking, and hostile tumor microenvironment. Excessive amount of research is going on to improve the efficacy of CAR T cell therapy in solid tumors. In this article, we will discuss the challenges faced in improving the outcome of CAR T cell therapy in solid tumors and various strategies adopted to curb them.
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页数:9
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