Insights into human CD8+ T-cell memory using the yellow fever and smallpox vaccines

被引:77
作者
Ahmed, Rafi [1 ,2 ,3 ]
Akondy, Rama S. [1 ,2 ]
机构
[1] Emory Univ, Emory Vaccine Ctr, Atlanta, GA 30322 USA
[2] Hope Clin, Atlanta, GA USA
[3] Emory Univ, Dept Microbiol & Immunol, Sch Med, Atlanta, GA 30322 USA
基金
美国国家卫生研究院;
关键词
CD8 T cells; immune memory; human; yellow fever vaccine; smallpox vaccine; T-cell differentiation; HEPATITIS-C-VIRUS; VIRAL-INFECTION; IMMUNOLOGICAL MEMORY; HIV-1; INFECTION; IN-VIVO; B-CELL; IMMUNITY; ANTIGEN; RESPONSES; DIFFERENTIATION;
D O I
10.1038/icb.2010.155
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Live virus vaccines provide a unique opportunity to study human CD8(+) T-cell memory in the context of a controlled, primary acute viral infection. Yellow fever virus-17D and Dryvax are two such live-virus vaccines that are highly efficacious, used worldwide and provide long-term immunity against yellow fever and smallpox respectively. In this review, we describe the properties of virus-specific memory CD8(+) T cells generated in smallpox and yellow fever vaccinees. We address fundamental questions regarding magnitude, functional quality and longevity of the CD8(+) T-cell response, which are otherwise challenging to address in humans. These findings provide insights into the attributes of the human immune system as well as provide a benchmark for the optimal quality of a CD8(+) T-cell response that can be used to evaluate novel candidate vaccines. Immunology and Cell Biology (2011) 89, 340-345; doi:10.1038/icb.2010.155; published online 8 February 2011
引用
收藏
页码:340 / 345
页数:6
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