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Clearance of persistent hepatitis C virus infection using a claudin-1-targeting monoclonal antibody

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2015

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Mailly, L., F. Xiao, J. Lupberger, G. K. Wilson, P. Aubert, F. H. T. Duong, D. Calabrese, et al. 2015. “Clearance of persistent hepatitis C virus infection using a claudin-1-targeting monoclonal antibody.” Nature biotechnology 33 (5): 549-554. doi:10.1038/nbt.3179. http://dx.doi.org/10.1038/nbt.3179.

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Abstract

Hepatitis C virus (HCV) infection is a leading cause of liver cirrhosis and cancer1. Cell entry of HCV2 and other pathogens3-5 is mediated by tight junction (TJ) proteins, but successful therapeutic targeting of TJ proteins has not been reported yet. Using a human liver-chimeric mouse model6 we show that a monoclonal antibody specific for TJ protein claudin-17 eliminates chronic HCV infection without detectable toxicity. This antibody inhibits HCV entry, cell-cell transmission and virus-induced signaling events. Antibody treatment reduces the number of HCV-infected hepatocytes in vivo, highlighting the need for de novo infection via host entry factors to maintain chronic infection. In summary, we demonstrate that an antibody targeting a virus receptor can cure chronic viral infection and uncover TJ proteins as targets for antiviral therapy.

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