Nicastro Emanuele, Severi Eleonora, Passera Ilaria, Totaro Michele, Matarazzo Lorenza, Fornataro Laura, Morotti Francesco, Tebaldi Alessandra, Bonanomi Ezio, Bravi Michela, Di Giorgio Angelo, Covini Samuele, Dolci Marta, Pinelli Domenico, Arosio Marco Enrico Giovanni, D'Antiga Lorenzo
Pediatric Hepatology, Gastroenterology and Transplantation, Hospital Papa Giovanni XXIII, Bergamo, Italy.
Department of Pediatrics, University of Milan Bicocca, Milan, Italy.
J Med Virol. 2025 Apr;97(4):e70347. doi: 10.1002/jmv.70347.
Preemptive therapy (PET) is safe and effective in controlling Cytomegalovirus (CMV) infection after pediatric liver transplantation (LT) and allows to observe the kinetics of quantitative CMV-DNA viral load till it reaches the treatment thresholds. While early detection of low-to-moderate CMV-DNA levels may not indicate active viral replication, awaiting the viral load to exceed the treatment threshold may lead to viremic breakthroughs and CMV disease. We assessed the capacity of quantitative CMV-RNA (UL21.5 mRNA) to identify active viral replication and its accuracy in identifying clinically significant CMV infection (csCMVi) needing PET in LT children. One-hundred and forty-four comparative quantitative CMV-RNA and CMV-DNA determinations were obtained from 12 children followed prospectically for 6 months after LT. Of 52 CMV-DNA-positive specimens, 17 (32%) were also CMV-RNA-positive, while CMV-RNA was undetectable in CMV-DNA-negative specimens. All children with csCMVi had early detectable CMV-RNA, peaking simultaneously to CMV-DNA (median CMV-DNA: 65 906 cp/mL; median CMV-RNA: 767 cp/mL); conversely, none of those with persistently low DNAemia proved CMV-RNA-positive. In this first pilot study, CMV-RNA had 100% sensitivity and specificity in identifying children needing PET after pediatric LT. The early detection of CMV-RNA marks significant CMV infection/reactivation, thus allowing to avoid unnecessary antiviral treatment.
抢先治疗(PET)在控制小儿肝移植(LT)后巨细胞病毒(CMV)感染方面安全有效,并能观察到CMV-DNA病毒载量的动力学变化直至达到治疗阈值。虽然早期检测到低至中度的CMV-DNA水平可能并不表明病毒在活跃复制,但等待病毒载量超过治疗阈值可能会导致病毒血症突破和CMV疾病。我们评估了定量CMV-RNA(UL21.5 mRNA)识别活跃病毒复制的能力及其在识别LT儿童中需要PET的临床显著CMV感染(csCMVi)方面的准确性。从12名LT后前瞻性随访6个月的儿童中获得了144次CMV-RNA和CMV-DNA的比较定量测定结果。在52份CMV-DNA阳性标本中,17份(32%)也为CMV-RNA阳性,而在CMV-DNA阴性标本中未检测到CMV-RNA。所有患有csCMVi的儿童均早期可检测到CMV-RNA,其峰值与CMV-DNA同时出现(CMV-DNA中位数:65 906拷贝/mL;CMV-RNA中位数:767拷贝/mL);相反,那些持续性低病毒血症的儿童均未被证明CMV-RNA阳性。在这项初步试验研究中,CMV-RNA在识别小儿LT后需要PET的儿童方面具有100%的敏感性和特异性。CMV-RNA的早期检测标志着显著的CMV感染/再激活,从而可避免不必要的抗病毒治疗。