Chen Sharon F, Holmes Tyson H, Slifer Teri, Ramachandran Vasavi, Mackey Sally, Hebson Cathleen, Arvin Ann M, Lewis David B, Dekker Cornelia L
Department of Pediatrics.
Psychiatry and Behavioral Sciences, Stanford University School of Medicine, Palo Alto, California.
J Pediatric Infect Dis Soc. 2016 Mar;5(1):14-20. doi: 10.1093/jpids/piu089. Epub 2014 Sep 11.
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.
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.
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.
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.
据报道,先天性巨细胞病毒(CMV)在美国所有活产婴儿中的感染率高达1%。T细胞免疫对于控制先天性CMV感染婴儿体内的CMV复制可能很重要。我们描述了先天性CMV感染婴儿中CMV特异性T细胞演变和CMV复制的自然史。
对51例先天性CMV感染婴儿进行前瞻性纵向队列研究,从出生至3岁观察其巨细胞病毒病毒载量、CMV尿培养以及CMV特异性CD4和CD8 T细胞反应。
我们发现,在生命的前3年中,尿中CMV复制减少,CMV特异性CD4和CD8 T细胞反应增加,呈现出一种动态变化模式。我们还发现,较高的CMV特异性CD8 T细胞反应与随后尿中CMV病毒载量的降低有关。
对于先天性CMV感染的婴儿,我们的数据表明,CMV特异性CD4和CD8 T细胞免疫与年龄相关的成熟,这与尿中CMV复制随年龄的下降有关。