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Quasispecies Diversity Is a Major Risk Factor for Vertical Hepatitis C Virus Transmission.

Authors :
Larouche, Ariane
McSween, Kimberly-Ann Milton
Calderon, Virginie
Fauteux-Daniel, Sébastien
Boulais, Jonathan
Ransy, Doris G
Boucher, Marc
Lamarre, Valérie
Lapointe, Normand
Boucoiran, Isabelle
Money, Deborah M
Krajden, Mel
Campion, Armelle Le
Soudeyns, Hugo
Source :
Journal of Infectious Diseases; Mar2019, Vol. 219 Issue 5, p760-771, 12p
Publication Year :
2019

Abstract

Background Vertical transmission is the major cause of pediatric hepatitis C virus (HCV) infection. The objective of this study was to better understand HCV pathogenesis in pregnant women and provide insights into risk factors and mechanisms involved in vertical transmission. Methods Evolutionary dynamics of HCV variant spectra and HCV-specific neutralizing antibody responses were examined using high-throughput sequencing and pseudoparticle-based assays in pregnant women monoinfected with HCV (n = 17) or coinfected with HCV and human immunodeficiency virus (HIV)-1 (n = 15). Results Overall, statistically significant associations were found between HCV quasispecies diversity, selective pressure exerted on the HCV E2 envelope protein, and neutralizing activity of maternal immunoglobulins. Women with low quasispecies diversity displayed significantly higher mean aspartate aminotransferase and alanine aminotransferase levels throughout pregnancy, but this difference was restricted to monoinfected participants. Low quasispecies diversity and inefficient neutralizing activity were also significantly associated with vertical transmission, but only in the monoinfected group. Conclusions These results indicate that maternal neutralizing antibody responses play a role in the prevention of vertical HCV transmission, but not in presence of HIV-1 coinfection, and suggest that the mechanism of vertical transmission may be different between monoinfected and coinfected women. These findings could inform management strategies for the prevention of vertical HCV transmission. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
00221899
Volume :
219
Issue :
5
Database :
Complementary Index
Journal :
Journal of Infectious Diseases
Publication Type :
Academic Journal
Accession number :
134756999
Full Text :
https://doi.org/10.1093/infdis/jiy581