Taming regulatory T cells by autologous T cell immunization: A potential new strategy for cancer immune therapy

被引:3
|
作者
Zhang, Yan [1 ]
Wang, Li [1 ]
Li, Dangsheng [2 ]
Li, Ningli [1 ]
机构
[1] Shanghai Jiao Tong Univ, Sch Med, Inst Med Sci, Shanghai Inst Immunol, Shanghai 200025, Peoples R China
[2] Chinese Acad Sci, Shanghai Inst Biol Sci, Shanghai, Peoples R China
基金
中国国家自然科学基金;
关键词
Tregs; Immune therapy; Autologous T cell; Immunization; Regulatory T cells; Anti-tumor immunity; MYELIN BASIC-PROTEIN; IMMUNOLOGICAL SELF-TOLERANCE; TRANSCRIPTION FACTOR FOXP3; PROGRESSIVE FIBRO-SARCOMA; AUTOIMMUNE ENCEPHALOMYELITIS; MULTIPLE-SCLEROSIS; TUMOR-IMMUNITY; VACCINATION; INDUCTION; RESPONSES;
D O I
10.1016/j.intimp.2009.01.026
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Regulatory T cells (Tregs) play important roles in the maintenance of immune homeostasis, and is also involved in tumor immune tolerance. Dampening or elimination of Treg functions has been shown to lead to enhanced immune responses against tumors, and thus inhibition of tumor growth. Recently, we have developed a new immunization scheme, referred to as irradiated mitogen-activated autologous T cell vaccination (ATCV), and shown that such immunization could significantly enhance anti-tumor immunity in vivo. Mechanistically, the enhanced anti-tumor response appears to be due to reduced Treg functions and inhibition of activation-induced cell death (AICD) in effector T cells. Thus, ATCV may constitute a novel strategy in cancer immune therapy. (C) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:593 / 595
页数:3
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