生物
细胞毒性T细胞
病毒学
CD8型
抗原
T细胞
主要组织相容性复合体
CTL公司*
免疫学
淋巴细胞性脉络膜脑膜炎
牛痘
脾脏
免疫系统
体外
重组DNA
基因
生物化学
作者
Kaja Murali‐Krishna,John D. Altman,M. Suresh,David Sourdive,Allan Zajac,Joseph D. Miller,Jill E. Slansky,Rafi Ahmed
出处
期刊:Immunity
[Elsevier]
日期:1998-02-01
卷期号:8 (2): 177-187
被引量:2008
标识
DOI:10.1016/s1074-7613(00)80470-7
摘要
Viral infections induce extensive T cell proliferation in vivo, but the specificity of the majority of the responding T cells has not been defined. To address this issue we used tetramers of MHC class I molecules containing viral peptides to directly visualize antigen-specific CD8 T cells during acute LCMV infection of mice. Based on tetramer binding and two sensitive assays measuring interferon-γ production at the single-cell level, we found that 50%–70% of the activated CD8 T cells were LCMV specific (2 × 107 virus-specific cells/spleen). Following viral clearance, antigen-specific CD8 T cell numbers dropped to 106 per spleen and were maintained at this level for the life of the mouse. Upon rechallenge with LCMV, there was rapid expansion of memory T cells, but after infection with the heterologous vaccinia virus there was no detectable change in the numbers of LCMV-specific memory CTL. Therefore, much of the CD8 T cell expansion seen during viral infection represents antigen-specific cells and warrants a revision of our current thinking on the size of the antiviral response.
科研通智能强力驱动
Strongly Powered by AbleSci AI