Engineered T cells for anti-cancer therapy

被引:57
作者
Turtle, Cameron J. [1 ,2 ]
Hudecek, Michael [1 ,3 ]
Jensen, Michael C. [1 ,2 ,4 ]
Riddell, Stanley R. [1 ,2 ,5 ]
机构
[1] Fred Hutchinson Canc Res Ctr, Div Clin Res, Program Immunol, Seattle, WA 98104 USA
[2] Univ Washington, Dept Med, Seattle, WA USA
[3] Univ Wurzburg, Dept Med 2, Wurzburg, Germany
[4] Seattle Childrens Res Inst, Ben Towne Ctr Childhood Canc Res, Seattle, WA USA
[5] Tech Univ Munich, Inst Adv Study, D-80290 Munich, Germany
基金
美国国家卫生研究院;
关键词
CHIMERIC-ANTIGEN-RECEPTOR; ADOPTIVE IMMUNOTHERAPY; METASTATIC MELANOMA; CANCER REGRESSION; ANTITUMOR-ACTIVITY; CLINICAL-TRIAL; TCR; IL-12; PERSISTENCE; EXPRESSION;
D O I
10.1016/j.coi.2012.06.004
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Recent advances enabling efficient delivery of transgenes to human T cells have created opportunities to address obstacles that previously hindered the application of T cell therapy to cancer. Modification of T cells with transgenes encoding TCRs or chimeric antigen receptors allows tumor specificity to be conferred on functionally distinct T cell subsets, and incorporation of costimulatory molecules or cytokines can enable engineered T cells to bypass local and systemic tolerance mechanisms. Clinical studies of genetically modified T cell therapy for cancer have shown notable success; however, these trials demonstrate that tumor therapy with engineered high avidity tumor-reactive T cells may be accompanied by significant on-target toxicity, necessitating careful selection of target antigens and development of strategies to eliminate transferred cells.
引用
收藏
页码:633 / 639
页数:7
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