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Cytomegalovirus (CMV) glycoprotein H-based serological analysis in Japanese healthy pregnant women, and in neonates with congenital CMV infection and their mothers

Authors :
Tatsuo Suzutani
Takashi Imamura
Toshio Minematsu
Shigeyoshi Fujiwara
Takahiko Kubo
Hiroyuki Moriuchi
Shin Koyano
Hidetaka Nakai
Kei Ishibashi
Kazufumi Ikuta
Tetsushi Yoshikawa
Kimisato Asano
Naoki Inoue
Source :
Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology. 58(2)
Publication Year :
2013

Abstract

Background Congenital cytomegalovirus (CMV) infection is caused by maternal primary infection as well as CMV reinfection or reactivation during pregnancy, although differences in the clinical impact between these modes of infection remain to be clarified. Objectives To investigate the latest prevalence and risk of multiple CMV infection in healthy pregnant women, as well as the types of maternal CMV infection associated with congenital CMV infection. Study design Seroprevalence against CMV and IgG subclasses were determined in 344 serum samples from healthy pregnant women in Japan. CMV genotype and serotype were also determined in 18 pairs of mothers and neonates with congenital CMV infection identified in our CMV screening program. Results Thirty-two percent of the pregnant women were seronegative, while 66% of CMV seropositive women had IgG3 antibodies against one epitope on glycoprotein H (gH) as the major subclass, and 52% had IgG1 antibodies against one epitope on glycoprotein B (gB). Only a single genotype determined by CMV gH neutralizing epitope was found in the urine from the 18 neonates with congenital CMV infection, even though one case possessed antibodies against multiple CMV strains. In that case, the antibodies against the strain not detected in the urine from the infant disappeared within one month after birth, whereas the antibodies against the infecting CMV strain continued to be detected at 12 months after birth. Conclusions Two (11%) of 18 cases of congenital CMV infection occurred via maternal CMV reinfection. Maternal humoral immunity did not prevent congenital CMV infection with another gH subtype.

Details

ISSN :
18735967
Volume :
58
Issue :
2
Database :
OpenAIRE
Journal :
Journal of clinical virology : the official publication of the Pan American Society for Clinical Virology
Accession number :
edsair.doi.dedup.....231216c0e12eb7e351f3a53e8415854c