Clinical application of genetically modified T cells in cancer therapy

被引:94
作者
Kershaw, Michael H. [1 ,2 ]
Westwood, Jennifer A. [1 ]
Slaney, Clare Y. [1 ]
Darcy, Phillip K. [1 ,2 ]
机构
[1] Univ Melbourne, Sir Peter MacCallum Canc Ctr, Dept Oncol, Melbourne, Vic, Australia
[2] Monash Univ, Dept Immunol, Prahran, Vic, Australia
基金
澳大利亚国家健康与医学研究理事会; 英国医学研究理事会;
关键词
adoptive cell transfer; chimeric antigen receptor; gene therapy;
D O I
10.1038/cti.2014.7
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunotherapies are emerging as highly promising approaches for the treatment of cancer. In these approaches, a variety of materials are used to boost immunity against malignant cells. A key component of many of these approaches is functional tumor-specific T cells, but the existence and activity of sufficient T cells in the immune repertoire is not always the case. Recent methods of generating tumor-specific T cells include the genetic modification of patient lymphocytes with receptors to endow them with tumor specificity. These T cells are then expanded in vitro followed by infusion of the patient in adoptive cell transfer protocols. Genes used to modify T cells include those encoding T-cell receptors and chimeric antigen receptors. In this review, we provide an introduction to the field of genetic engineering of T cells followed by details of their use against cancer in the clinic.
引用
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页数:7
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