Striking immunodominance hierarchy of naturally occurring CD8+ and CD4+ T cell responses to tumor antigen NY-ESO-1

被引:33
作者
Jackson, Heather
Dimopoulos, Nektaria
Mifsud, Nicole A.
Tai, Tsin Yee
Chen, Qiyuan
Svobodova, Suzanne
Browning, Judy
Luescher, Immanuel
Stockert, Lisa
Old, Lloyd J.
Davis, Ian D.
Cebon, Jonathan
Chen, Weisan
机构
[1] Ludwig Inst Canc Res, Austin Hlth, Heidelberg, Vic 3084, Australia
[2] Dept Pathol, Austin Hlth, Heidelberg, Germany
[3] Ludwig Inst Canc Res, Lausanne, Switzerland
[4] Ludwig Inst Canc Res, New York, NY 10021 USA
基金
英国惠康基金;
关键词
D O I
10.4049/jimmunol.176.10.5908
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Immunodominance has been well-demonstrated in many antiviral and antibacterial systems, but much less so in the setting of immune responses against cancer. Tumor Ag-specific CD8(+) T cells keep cancer cells in check via immunosurveillance and shape tumor development through immunoediting. Because most tumor Ags are self Ags, the breadth and depth of antitumor immune responses have not been well-appreciated. To design and develop antitumor vaccines, it is important to understand the immunodominance hierarchy and its underlying mechanisms, and to identify the most immunodominant tumor Ag-specific T cells. We have comprehensively analyzed spontaneous cellular immune responses of one individual and show that multiple tumor Ags are targeted by the patient's immune system, especially the "cancer-testis" tumor Ag NY-ESO-1. The pattern of anti-NY-ESO-1 T cell responses in this patient closely resembles the classical broad yet hierarchical antiviral immunity and was confirmed in a second subject.
引用
收藏
页码:5908 / 5917
页数:10
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