Antiviral CD8 T cells in the control of primary human cytomegalovirus infection in early childhood

被引:40
作者
Chen, SF
Tu, WW
Sharp, MA
Tongson, EC
He, XS
Greenberg, HB
Holmes, TH
Wang, ZT
Kemble, G
Manganello, AM
Adler, SP
Dekker, CL
Levvis, DB
Arvin, AM
机构
[1] Stanford Univ, Sch Med, Dept Pediat, Stanford, CA 94305 USA
[2] Stanford Univ, Sch Med, Dept Med, Stanford, CA 94305 USA
[3] Stanford Univ, Sch Med, Dept Hlth Res & Policy, Div Biostat, Stanford, CA 94305 USA
[4] MedImmune Vaccines, Mountain View, CA USA
[5] Virginia Commonwealth Univ, Dept Pediat, Richmond, VA 23284 USA
关键词
D O I
10.1086/383249
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Human cytomegalovirus (CMV) establishes persistent infection, with control of replication thought to be mediated by CMV-specific CD8 T cells. Primary CMV infection commonly affects young children and causes prolonged viral shedding in saliva and urine. We investigated whether this virus-host interaction pattern reflects a developmental deficiency of antiviral CD8 T cell-mediated immunity during childhood. CMV-specific CD8 T cell responses in asymptomatic children with active infection were not different from adults with recent or long-term infection in frequency and functional analyses. High urine CMV concentrations were detected, despite these CMV-specific CD8 T cell responses. We conclude that delayed resolution of primary CMV infection in young children is not caused by a deficient CMV-specific CD8 T cell response. Because these healthy children continue to have local CMV replication, we suggest that CD8 T cells may function primarily to prevent symptomatic, disseminated disease.
引用
收藏
页码:1619 / 1627
页数:9
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