Abstract

Congenital cytomegalovirus (cCMV) is the leading non-genetic cause of sensorineural hearing loss (SNHL), and efforts are geared towards prevention through vaccine development. Transmission rates following primary maternal infection occur at rates of 30–40%, however reported placental rates upon non-primary maternal infection is reported to be less than <4%. There is significant debate about whether this reduction in transmission rate is due to pre-existing maternal immunity, which could identify possible immunologic targets for vaccines. To address this question, we performed a systemic review of the literature using Preferred Reporting Items for Systematic Review and Analysis (PRISMA) guidelines. We identified cohort studies in high CMV seroprevalent (>80%) areas or in developing regions that examined a cohort of at least 50 infants for congenital CMV acquisition. We identified 19 articles that met criteria and were further categorized based on pre-conception serology, maternal seroprevalence, or previously known seroprevalence. Birth prevalence rates ranged from 0.4% to 6% (median 1.1%), with the studies reporting on clinical outcome (16/19 studies) noting the majority of infected infants as asymptomatic. We also utilized a recent study that differentiated primary maternal infections from chronic infections in a highly seropositive population to calculate a placental transmission rate in women with pre-existing immunity compared to that of no pre-existing immunity. This work confirms a low cCMV birth prevalence in highly seropositive populations, indicates via a calculated placental transmission rate that the CMV placental transmission rate is lower in non-primary infection than that of primary infection, and reveals gaps in data for further research aiming to identify targets for vaccine development.

Highlights

  • Congenital cytomegalovirus is the most common infectious cause of birth defects [1,2,3,4].cCMV infection affects 5–7 of every 1000 live births in the United States and 0.5–2% of live births worldwide [5,6,7]

  • Birth prevalence rates ranged from 0.4% to 6%, with the studies reporting on clinical outcome (16/19 studies) noting the majority of infected infants as asymptomatic

  • This work confirms a low cCMV birth prevalence in highly seropositive populations, indicates via a calculated placental transmission rate that the CMV placental transmission rate is lower in non-primary infection than that of primary infection, and reveals gaps in data for further research aiming to identify targets for vaccine development

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Summary

Introduction

Congenital cytomegalovirus (cCMV) is the most common infectious cause of birth defects [1,2,3,4].cCMV infection affects 5–7 of every 1000 live births in the United States and 0.5–2% of live births worldwide [5,6,7]. 85–90% of infants born with cCMV are asymptomatic, while only 10% of infants are symptomatic at birth [9,10]. Of those infants who demonstrate CMV-associated sequelae at birth, 40–60% will develop permanent sequelae including cerebral palsy, cognitive impairment, microcephaly and sensorineural hearing loss (SNHL) [7,10,11]. Those who are born asymptomatic are at risk of developing sequelae; as 6–23% of asymptomatic infants eventually develop SNHL. CCMV is the Vaccines 2019, 7, 129; doi:10.3390/vaccines7040129 www.mdpi.com/journal/vaccines

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