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新生儿巨细胞病毒感染:用于早期疾病检测的诊断方法。

Neonatal cytomegalovirus infection: diagnostic modalities available for early disease detection.

机构信息

Department of Immunopathology, Post Graduate Institute of Medical Education and Research, Chandigarh, India.

出版信息

Indian J Pediatr. 2010 Jan;77(1):77-9. doi: 10.1007/s12098-009-0255-2.

Abstract

CMV is a ubiquitous virus. In India, there is high seroendemicity with almost 99% adults showing IgG antibodies. Infection or re-activation becomes important in immunocompromised host (Transplant recipients, Cancer therapy patients and patients with HIV/AIDS). Neonates form a distinctive high risk population for congenital CMV infection and suffer disastrous sequlae of the same. Neonatal infections may be congenital in nature or may be acquired after birth during first month of life via infected breast milk or due to exposure to high risk blood products. The risk for transmission of the virus to the fetus is higher in primary infected mothers than in mothers with reactivated disease. Primary CMV infections are reported in 1-4% of seronegative women during pregnancy and the risk for viral transmission to fetus is 30-40%. Reactivation of a CMV infection during pregnancy is reported in 10-30% of seropositive women and the risk of transmitting the virus is about 1-3%. The adverse outcome of congenital neonatal CMV infection includes-microcephaly (70%), intellectual impairment (60%), sensineural hearing loss (35%), choriorenitis (22%), hepatosplenomegaly (70%), jaundice (68%), thrombocytopenia (65%), low birth weight (65%), pneumonitis (2-5%) and congenital heart disease (<5%). About 5-10% of congenitally infected asymptomatic infants will have neurological problems later in life the most common of which is unilateral or bilateral sensory neural hearing loss. All immunocompromised hosts, including pre-term neonates, mount weak antibody responses (IgM), making serological detection of CMV infection in them, fallacious. Thus, it is imperative to use antigen detection methods such as quantitative PCR or PP65 Antigenaemia assays to detect CMV infection in immunocompromised host. Sakhuja et al and Minz et al have demonstrated that PP65 Antigenaemia assay is very good for diagnosing CMV disease in renal transplant recipients. The present review tends to highlight the role of newer diagnostic modalities in early CMV infection detection in neonatal population.

摘要

巨细胞病毒是一种普遍存在的病毒。在印度,几乎 99%的成年人都显示出 IgG 抗体,存在高度的血清流行率。在免疫功能低下的宿主(移植受者、癌症治疗患者和艾滋病毒/艾滋病患者)中,感染或再激活变得很重要。新生儿是先天性巨细胞病毒感染的高风险人群,会遭受灾难性的后果。新生儿感染可能是先天性的,也可能是在出生后第一个月内通过受感染的母乳或由于接触高危血液制品而获得的。在原发性感染的母亲中,病毒向胎儿传播的风险高于在患有再激活疾病的母亲中。在怀孕期间,1-4%的血清阴性妇女报告有原发性 CMV 感染,病毒向胎儿传播的风险为 30-40%。在血清阳性妇女中,有 10-30%报告有 CMV 感染再激活,病毒传播的风险约为 1-3%。先天性新生儿 CMV 感染的不良后果包括-小头畸形(70%)、智力障碍(60%)、感觉神经性听力损失(35%)、脉络膜炎(22%)、肝脾肿大(70%)、黄疸(68%)、血小板减少症(65%)、低出生体重(65%)、肺炎(2-5%)和先天性心脏病(<5%)。大约 5-10%的先天性无症状感染婴儿以后会出现神经问题,最常见的是单侧或双侧感觉神经性听力损失。所有免疫功能低下的宿主,包括早产儿,都会产生较弱的抗体反应(IgM),使得血清学检测 CMV 感染在他们身上变得不可靠。因此,必须使用抗原检测方法,如定量 PCR 或 PP65 抗原血症检测,来检测免疫功能低下宿主的 CMV 感染。Sakhuja 等人和 Minz 等人已经证明,PP65 抗原血症检测对于诊断肾移植受者的 CMV 疾病非常有效。本综述旨在强调在新生儿人群中早期 CMV 感染检测的新诊断方法的作用。

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