Effective control of viral infections by the adaptive immune system requires assistance from innate immunity

被引:1
|
作者
Barra, Nicole G. [1 ,2 ]
Gillgrass, Amy [1 ,2 ]
Ashkar, Ali A. [1 ,2 ]
机构
[1] McMaster Univ, Ctr Gene Therapeut, Hamilton, ON L8N 3Z5, Canada
[2] McMaster Univ, Inst Infect Dis Res, Hamilton, ON L8N 3Z5, Canada
基金
加拿大健康研究院;
关键词
CD8(+) T cells; effector T cells; LCMV; memory T cells; PKR; type I IFNs; NATURAL-KILLER-CELLS; CD8; T-CELLS; CLONAL EXPANSION; CUTTING EDGE; PROTEIN; RESPONSES; ALPHA/BETA; PROTECTION; VIRUSES; DEFENSE;
D O I
10.1586/ERV.10.119
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
During acute viral infections, innate antiviral immunity has been extensively studied for its ability to inhibit and/or control viral replication while priming the adaptive immune system. Recently, these processes have been studied for their role in assisting adaptive immunity to effectively clear or control viral rechallenge. The paper under evaluation introduces the concept that functional innate immune mechanisms such as dsRNA-activated protein kinase (PKR) and type I interferons are critical in controlling viral replication during secondary lymphocyte choriomeningitis virus infection. Elegant adoptive transfer studies revealed that during lymphocyte choriomeningitis virus secondary infections, dependence of viral control relied on expression of these innate factors in virally infected cells and not in adaptive immune T cells. Such findings illustrate that functional adaptive responses are less effective in providing protection against reinfections in the absence of innate mechanisms. This demonstrates the importance of intact innate mechanisms when considering effective vaccine strategies.
引用
收藏
页码:1143 / 1147
页数:5
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