Successful anti‐scavenger receptor class B type I (SR‐BI) monoclonal antibody therapy in humanized mice after challenge with HCV variants with in vitro resistance to SR‐BI‐targeting agents. Issue 5 (30th July 2014)

• Record Type: Journal Article
• Authors: Vercauteren, Koen; Van Den Eede, Naomi; Mesalam, Ahmed Atef; Belouzard, Sandrine; Catanese, Maria Teresa; Bankwitz, Dorothea; Wong‐Staal, Flossie; Cortese, Riccardo; Dubuisson, Jean; Rice, Charles M.; Pietschmann, Thomas; Leroux‐Roels, Geert; Nicosia, Alfredo; Meuleman, Philip
• Is Part Of: Hepatology. Volume 60:Issue 5(2014:Nov.)
• Page Start: 1508
• Page End: 1518
• Publication Date: 2014-07-30
• Subjects: Heart -- Diseases -- Nursing -- Periodicals; Lungs -- Diseases -- Nursing -- Periodicals; Intensive care nursing -- Periodicals; Foie -- Maladies -- Périodiques; 616.362
• DOI: 10.1002/hep.27196
• Languages: English
• ISSNs: 0270-9139

Abstract

<abstract abstract-type="main"> <title> <x xml:space="preserve">Abstract</x> </title> <p>Hepatitis C virus (HCV)‐induced endstage liver disease is currently a major indication for liver transplantation. After transplantation the donor liver inevitably becomes infected with the circulating virus. Monoclonal antibodies (mAbs) against the HCV coreceptor scavenger receptor class B type I (SR‐BI) inhibit HCV infection of different genotypes, both in cell culture and in humanized mice. Anti‐SR‐BI mAb therapy is successful even when initiated several days after HCV exposure, supporting its potential applicability to prevent HCV reinfection of liver allografts. However, HCV variants with reduced SR‐BI dependency have been described in the literature, which could potentially limit the use of SR‐BI targeting therapy. In this study we show, both in a preventative and postexposure setting, that humanized mice infected with HCV variants exhibiting increased <italic>in vitro</italic> resistance to SR‐BI‐targeting molecules remain responsive to anti‐SR‐BI mAb therapy <italic>in vivo</italic>. A 2‐week antibody therapy readily cleared HCV RNA from the circulation of infected humanized mice. We found no evidence supporting increased SR‐BI‐receptor dependency of viral particles isolated from humanized mice compared to cell culture‐produced virus. However, we observed that, unlike wild‐type virus, the <italic>in vitro</italic> infectivity of the resistant variants was inhibited by both human high density lipoprotein (HDL) and very low density lipoprotein (VLDL). The combination of mAb1671 with these lipoproteins further increased the antiviral effect. <italic>Conclusion</italic>: HCV variants that are less dependent on SR‐BI <italic>in vitro</italic> can still be efficiently blocked by an anti‐SR‐BI mAb in humanized mice. Since these variants are also more susceptible to neutralization by anti‐HCV envelope antibodies, their chance of emerging during anti‐SR‐BI therapy is severely reduced. Our data indicate that anti‐SR‐BI receptor therapy could be an effective way to prevent HCV infection in a liver transplant setting. (Hepatology 2014;60:1508–1518)</p> </abstract>