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Anticancer research · Jun 2012
ReviewFunctional design of chimeric T-cell antigen receptors for adoptive immunotherapy of cancer: architecture and outcomes.
- Naoto Shirasu and Masahide Kuroki.
- Department of Biochemistry, Faculty of Medicine, Fukuoka University, 7-45-1 Jonan-ku, Fukuoka 814-0180, Japan. shirasu@fukuoka-u.ac.jp
- Anticancer Res. 2012 Jun 1; 32 (6): 2377-83.
AbstractAdoptive immunotherapy using genetically modified T-cells with a chimeric antigen receptor (CAR) is a promising modality for cancer treatment, because the CAR-grafted T-cells can directly recognize and kill tumor cells, expressing a specific tumor-associated antigen (TAA), in a human leukocyte antigen (HLA)-independent manner. Optimal molecular designs of the CAR and a careful choice of the target TAA are requisite to attain a significant response in CAR-mediated therapy. This review provides a brief overview of the past studies and the present state of CAR research, especially focusing on the development of the CAR protein architecture.
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