Hepatitis C virus-like particles synthesized in insect cells as a potential vaccine candidate

Background & Aims: Hepatitis C virus (HCV) is a leading cause of chronic hepatitis in the world. Successful vaccine development is crucial in controlling global HCV infection. We have previously described the generation of HCV-like particles (HCV-LPs) in insect cells using a recombinant baculovi...

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Veröffentlicht in:Gastroenterology (New York, N.Y. 1943) N.Y. 1943), 1999-12, Vol.117 (6), p.1397-1407
Hauptverfasser: Baumert, Thomas F., Vergalla, John, Satoi, Jujin, Thomson, Michael, Lechmann, Martin, Herion, David, Greenberg, Harry B., Ito, Susumu, Liang, T.Jake
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Sprache:eng
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Zusammenfassung:Background & Aims: Hepatitis C virus (HCV) is a leading cause of chronic hepatitis in the world. Successful vaccine development is crucial in controlling global HCV infection. We have previously described the generation of HCV-like particles (HCV-LPs) in insect cells using a recombinant baculovirus containing the complementary DNA of the HCV structural proteins. These HCV-LPs had similar morphological and biophysical properties as the putative virions. In this study, we analyzed the structural features, antigenic composition, seroreactivity, and immunogenicity of purified HCV-LPs. Methods: HCV-LPs were analyzed by electron microscopy and antibody immunolabeling and precipitation. An enzyme-linked immunosorbent assay (ELISA) using HCV-LPs was developed. The humoral response to HCV-LPs in mice was studies by core and envelope ELISAs, Western immunoblotting, and immunofluorescence. Results: Structural and antigenic compositions of HCV-LPs were shown to be similar to those of putative HCV virions. Using the HCV-LP ELISA, high-titer anti-HCV antibodies were detected in individuals infected with various HCV genotypes. In vivo, HCV-LPs elicited a humoral response broadly directed against HCV structural proteins. Conclusions: HCV-LPs resemble HCV virions and are capable of inducing a humoral response targeted against various regions of HCV structural proteins, suggesting that HCV-LPs may be promising as a potential vaccine candidate. GASTROENTEROLOGY 1999;117:1397-1407
ISSN:0016-5085
1528-0012
DOI:10.1016/S0016-5085(99)70290-8