Neonatal Unit, Department of Medical and Surgical Sciences, St.Orsola Polyclinic, University of Bologna, Bologna, Italy.
Operative Unit of Clinical Microbiology, Department of Specialized, Experimental and Diagnostic Medicine, St.Orsola Polyclinic, University of Bologna, Bologna, Italy.
Clin Infect Dis. 2021 Aug 2;73(3):367-373. doi: 10.1093/cid/ciaa704.
Cytomegalovirus (CMV)-specific CD8 + T-cell responses can be detected early in fetal life, but their role in the manifestations of congenital CMV (cCMV) infection remains largely unknown.
CMV-specific CD8 + T-cell responses were assessed in neonates with cCMV using QuantiFERON®-CMV assay, within day 14 of life (T0) and during the second month of life (T1). Detection and quantification of CMV DNA in whole blood and urine samples were performed at both time points. QuantiFERON®-CMV results were evaluated in relation to timing of maternal infection, clinical manifestations of cCMV and CMV DNA levels.
Thirty neonates were enrolled (10/30 [33%] symptomatic; 20/30 [67%] asymptomatic). At T0 16/30 (53%) subjects had a reactive QuantiFERON®-CMV result and 16/16 (100%) were asymptomatic, whereas 14/30 (47%) had a nonreactive or indeterminate QuantiFERON®-CMV result and 4/14 (29%) were asymptomatic. At T1, 17/29 (59%) subjects had a reactive QuantiFERON®-CMV result, and 17/17 (100%) were asymptomatic, whereas 12/29 (41%) had a nonreactive or indeterminate result and 3/12 (25%) were asymptomatic. At both T0 and T1 reactive QuantiFERON®-CMV results correlated with lack of symptoms (P = .0001). At T1 median CMV DNAemia was lower in subjects with reactive QuantiFERON®-CMV results as compared with subjects with nonreactive or indeterminate results (1.82 log IU/mL [1.82-2.89] vs 2.55 log IU/mL [1.82-4.42], P = .009). No correlation was found between QuantiFERON®-CMV results and gestational age at maternal infection nor with urine CMV DNA levels.
A detectable CMV-specific CD8 + T-cell response, evaluated using the QuantiFERON®-CMV assay, correlates with the lack of CMV-related symptoms and the control of CMV DNAemia.
巨细胞病毒(CMV)特异性 CD8+T 细胞反应可在胎儿期早期被检测到,但它们在先天性 CMV(cCMV)感染的表现中的作用仍知之甚少。
在出生后 14 天(T0)和第二个月(T1),使用 QuantiFERON®-CMV 检测法评估患有 cCMV 的新生儿的 CMV 特异性 CD8+T 细胞反应。在两个时间点均检测全血和尿液样本中的 CMV DNA 的存在和定量。评估 QuantiFERON®-CMV 结果与母体感染的时间、cCMV 的临床表现和 CMV DNA 水平之间的关系。
共纳入 30 名新生儿(33%[10/30]有症状;67%[20/30]无症状)。在 T0 时,16/30(53%)患者的 QuantiFERON®-CMV 检测结果为阳性,且 16/16(100%)无症状,而 14/30(47%)的结果为阴性或不确定,其中 4/14(29%)无症状。在 T1 时,29 名患者中有 17 名(59%)的 QuantiFERON®-CMV 检测结果为阳性,且 17/17(100%)无症状,而 12/29(41%)的结果为阴性或不确定,其中 3/12(25%)无症状。在 T0 和 T1 时,阳性 QuantiFERON®-CMV 检测结果与无症状相关(P=0.0001)。与阴性或不确定的 QuantiFERON®-CMV 结果相比,T1 时阳性 QuantiFERON®-CMV 检测结果的患者的 CMV DNA 血症中位数更低(1.82log IU/mL[1.82-2.89] vs 2.55log IU/mL[1.82-4.42],P=0.009)。QuantiFERON®-CMV 结果与母体感染时的胎龄或尿液 CMV DNA 水平均无相关性。
使用 QuantiFERON®-CMV 检测法评估的可检测到的 CMV 特异性 CD8+T 细胞反应与无 CMV 相关症状和控制 CMV DNA 血症相关。