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A Role for B Cells to Transmit Hepatitis C Virus Infection.

Authors :
Desombere I
Van Houtte F
Farhoudi A
Verhoye L
Buysschaert C
Gijbels Y
Couvent S
Swinnen W
Van Vlierberghe H
Elewaut A
Magri A
Stamataki Z
Meuleman P
McKeating JA
Leroux-Roels G
Source :
Frontiers in immunology [Front Immunol] 2021 Dec 16; Vol. 12, pp. 775098. Date of Electronic Publication: 2021 Dec 16 (Print Publication: 2021).
Publication Year :
2021

Abstract

Hepatitis C virus (HCV) is highly variable and transmits through infected blood to establish a chronic liver infection in the majority of patients. Our knowledge on the infectivity of clinical HCV strains is hampered by the lack of in vitro cell culture systems that support efficient viral replication. We and others have reported that HCV can associate with and infect immune cells and may thereby evade host immune surveillance and elimination. To evaluate whether B cells play a role in HCV transmission, we assessed the ability of B cells and sera from recent (<2 years) or chronic (≥ 2 years) HCV patients to infect humanized liver chimeric mice. HCV was transmitted by B cells from chronic infected patients whereas the sera were non-infectious. In contrast, B cells from recently infected patients failed to transmit HCV to the mice, whereas all serum samples were infectious. We observed an association between circulating anti-glycoprotein E1E2 antibodies and B cell HCV transmission. Taken together, our studies provide evidence for HCV transmission by B cells, findings that have clinical implications for prophylactic and therapeutic antibody-based vaccine design.<br />Competing Interests: The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.<br /> (Copyright © 2021 Desombere, Van Houtte, Farhoudi, Verhoye, Buysschaert, Gijbels, Couvent, Swinnen, Van Vlierberghe, Elewaut, Magri, Stamataki, Meuleman, McKeating and Leroux-Roels.)

Details

Language :
English
ISSN :
1664-3224
Volume :
12
Database :
MEDLINE
Journal :
Frontiers in immunology
Publication Type :
Academic Journal
Accession number :
34975862
Full Text :
https://doi.org/10.3389/fimmu.2021.775098