细胞毒性T细胞
CD8型
慢性感染
免疫学
效应器
免疫系统
生物
病毒
免疫
病毒学
病毒感染
T细胞
细胞
体外
生物化学
遗传学
作者
Heidi Elsaesser,Karsten Sauer,David G. Brooks
出处
期刊:Science
[American Association for the Advancement of Science]
日期:2009-05-08
卷期号:324 (5934): 1569-1572
被引量:540
标识
DOI:10.1126/science.1174182
摘要
CD4+ and CD8+ T cell functions are rapidly aborted during chronic infection, preventing viral clearance. CD4+ T cell help is required throughout chronic infection so as to sustain CD8+ T cell responses; however, the necessary factor(s) provided by CD4+ T cells are currently unknown. Using a mouse model of chronic viral infection, we demonstrated that interleukin-21 (IL-21) is an essential component of CD4+ T cell help. In the absence of IL-21 signaling, despite elevated CD4+ T cell responses, CD8+ T cell responses are severely impaired. CD8+ T cells directly require IL-21 to avoid deletion, maintain immunity, and resolve persistent infection. Thus, IL-21 specifically sustains CD8+ T cell effector activity and provides a mechanism of CD4+ T cell help during chronic viral infection.
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