Longitudinal Kinetics of Cytomegalovirus-Specific T-Cell Immunity and Viral Replication in Infants With Congenital Cytomegalovirus Infection

被引:9
作者
Chen, Sharon F. [1 ]
Holmes, Tyson H. [2 ]
Slifer, Teri [1 ]
Ramachandran, Vasavi [1 ]
Mackey, Sally [1 ]
Hebson, Cathleen [3 ]
Arvin, Ann M. [1 ]
Lewis, David B. [1 ]
Dekker, Cornelia L. [1 ]
机构
[1] Stanford Univ, Sch Med, Dept Pediat, Palo Alto, CA 94304 USA
[2] Stanford Univ, Sch Med, Psychiat & Behav Sci, Palo Alto, CA 94304 USA
[3] Santa Clara Valley Med Ctr, Dept Pediat, San Jose, CA 95128 USA
基金
美国国家卫生研究院;
关键词
CMV-specific T cells; congenital CMV; kinetics; PCR; T cells; MEDIATED-IMMUNITY; HEARING-LOSS; RESPONSES; VIRUS; CHILDREN; CD4(+); CMV; RECIPIENTS; THERAPY;
D O I
10.1093/jpids/piu089
中图分类号
R51 [传染病];
学科分类号
100401 ;
摘要
Background. Congenital cytomegalovirus (CMV) is reported to affect up to 1% of all live births in the United States. T-cell immunity may be important for controlling CMV replication in congenital CMV-infected infants. We describe the natural history of CMV-specific T-cell evolution and CMV replication in infants with congenital CMV infection. Methods. Cytomegalovirus viral load, CMV urine culture, and CMV-specific CD4 and CD8 T-cell responses were assessed in a prospective longitudinal cohort of 51 infants with congenital CMV infection who were observed from birth to 3 years of age. Results. We found a kinetic pattern of decreasing urinary CMV replication and increasing CMV-specific CD4 and CD8 T-cell responses during the first 3 years of life. We also found higher CMV-specific CD8 T-cell responses were associated with subsequent reduction of urine CMV viral load. Conclusion. For infants with congenital CMV infection, our data suggest an age-related maturation of both CMV-specific CD4 and CD8 T-cell immunity that is associated with an age-related decline in urinary CMV replication.
引用
收藏
页码:14 / 20
页数:7
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