Precursor Frequency and Competition Dictate the HLA-A2-Restricted CD8+ T Cell Responses to Influenza A Infection and Vaccination in HLA-A2.1 Transgenic Mice

被引:42
|
作者
Tan, Amabel C. L. [1 ]
La Gruta, Nicole L. [1 ]
Zeng, Weiguang [1 ]
Jackson, David C. [1 ]
机构
[1] Univ Melbourne, Dept Microbiol & Immunol, Parkville, Vic 3010, Australia
来源
JOURNAL OF IMMUNOLOGY | 2011年 / 187卷 / 04期
基金
英国医学研究理事会;
关键词
MINOR HISTOCOMPATIBILITY ANTIGENS; VIRUS MATRIX PROTEIN; HEPATITIS-C VIRUS; CTL RESPONSE; LYMPHOCYTE RESPONSES; SEQUENCE VARIATION; BINDING-AFFINITY; DENDRITIC CELLS; ANTIVIRAL CTL; HLA-A;
D O I
10.4049/jimmunol.1100664
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The human HLA-A2-restricted CD8(+) T cell response to influenza A virus (IAV) is largely directed against the matrix protein-derived M1(58-66) epitope and represents an archetypal example of CD8(+) T cell immunodominance. In this study, we examined the CD8(+) T cell hierarchy to M1(58-66) and two subdominant IAV-specific epitopes: NS1(122-130) and PA(46-55) in HLA-A2(+) human subjects and HLA-A2.1 transgenic (HHD) mice. Using epitope-based lipopeptides, we show that the CD8(+) T cell hierarchy induced by IAV infection could also be induced by lipopeptide vaccination in a context outside of viral infection when the Ag load is equalized. In the HHD HLA-A2.1 mouse model, we show that the naive T cell precursor frequencies, and competition at the Ag presentation level, can predict the IAV-specific CD8(+) T cell hierarchy. Immunization of mice with subdominant epitopes alone was unable to overcome the dominance of the M1(58-66)-specific response in the face of IAV challenge; however, a multiepitope vaccination strategy was most effective at generating a broad and multispecific response to infection. The Journal of Immunology, 2011, 187: 1895-1902.
引用
收藏
页码:1895 / 1902
页数:8
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