Use of tumour-responsive T cells as cancer treatment

被引:140
作者
Disis, Mary L. [1 ]
Bernhard, Helga [2 ,3 ]
Jaffee, Elizabeth M. [4 ]
机构
[1] Univ Washington, Ctr Translat Med Womens Hlth, Tumor Vaccine Grp, Seattle, WA 98109 USA
[2] Tech Univ Munich, Dept Haematol Oncol, Klinikum Rechts Isar, Munich, Germany
[3] GSF Munich, Inst Hlth & Environm, Clin Cooperat Grp Antigen Specif Immunotherapy, Munich, Germany
[4] Johns Hopkins Univ, Sidney Kimmel Canc Ctr, Baltimore, MD USA
基金
美国国家卫生研究院;
关键词
D O I
10.1016/S0140-6736(09)60404-9
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
The stimulation of a tumour-specific T-cell response has several theoretical advantages over other forms of cancer treatment. First, T cells can home in to antigen-expressing tumour deposits no matter where they are located in the body-even in deep tissue beds. Additionally, T cells can continue to proliferate in response to immunogenic proteins expressed in cancer until all the tumour cells are eradicated. Finally, immunological memory can be generated, allowing for eradication of antigen-bearing tumours if they reoccur. We will highlight two direct methods of stimulating tumour-specific T-cell immunity: active immunisation with cancer vaccines and infusion of competent T cells via adoptive T-cell treatment. Preclinical and clinical studies have shown that modulation of the tumour microenvironment to support the immune response is as important as stimulation of the most appropriate effector T cells. The future of T-cell immunity stimulation to treat cancer will need combination approaches focused on both the tumour and the T cell.
引用
收藏
页码:673 / 683
页数:11
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