Central and Effector Memory CD4 and CD8 T-Cell Responses to Tumor-Associated Antigens

被引:39
|
作者
Caserta, Stefano [1 ]
Borger, Jessica Geraldine [1 ]
Zamoyska, Rose [1 ]
机构
[1] Univ Edinburgh, Inst Immunol & Infect Res, Edinburgh EH9 3JT, Midlothian, Scotland
基金
英国医学研究理事会;
关键词
Memory T cells; cancer; self-renewal; T-cell differentiation; immunotherapy; adoptive cell therapy; EX-VIVO EXPANSION; METASTATIC MELANOMA; IN-VIVO; INFILTRATING LYMPHOCYTES; ADOPTIVE IMMUNOTHERAPY; ANTITUMOR IMMUNITY; CUTTING EDGE; SECONDARY EXPANSION; DENDRITIC CELLS; CCR5; EXPRESSION;
D O I
10.1615/CritRevImmunol.v32.i2.10
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Harnessing T-cell responses to constrain tumor growth is a realistic treatment aspiration in tumor medicine, as many tumors express specific tumor associated antigens that are recognized by the adaptive immune system. CD8 T cells have direct cytolytic activity against tumor cells, and CD4 T cells mount a variety of responses that have important influences on tumor growth. We discuss how individual T-cell subsets contribute to antitumor responses and the goals and problems associated with generating and/or maintaining effective multifunctional T-cell responses to provide long-term protection against tumors.
引用
收藏
页码:97 / 126
页数:30
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