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• W2029989019 abstract "The sequence encoding the truncated core protein (amino acids 1–98) of hepatitis C virus (HCc) was expressed in E. coli for production of HCc(1–98), or fused with the truncated core antigen (HBcAg) and segments from the preS1 and preS2 regions from hepatitis B virus (HBV) for production of HBcPreS1PreS2HCc(1–98). The HCc(1–98) and HBcPreS1PreS2HCc(1–98) proteins reacted with sera from HCV-infected individuals by immunoblot analyses, while the latter protein also exhibited HBV core antigenicity. They induced antibodies against HBcAg and/or HCV core protein in rabbits and in mice. Moreover, HBcPreS1PreS2HCc(1–98) is more immunogenic than HCc(1–98) in terms of anti-HCc induction. An ELISA that employed recombinant HCV core antigens of either HCc(1–98) or HBcPreS1PreS2HCc(1–98) to detect anti-HCc and/or anti-HBc antibodies was developed. Evaluation of serum samples with different status of HBV and HCV infections suggested that HCc(1–98) might be suitable for the determination of antibodies against HCV core protein, while HBcPreS1PreS2HCc(1–98) might be of value to detect HCV and/or HBV infection in donated blood in HBV low-prevalence countries. J. Med. Virol. 57:104–110, 1999. © 1999 Wiley-Liss, Inc." @default.
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• W2029989019 date "1999-02-01" @default.
• W2029989019 modified "2023-09-25" @default.
• W2029989019 title "Hepatitis C virus core protein fused to hepatitis B virus core antigen for serological diagnosis of both hepatitis C and hepatitis B infections by ELISA" @default.
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• W2029989019 doi "https://doi.org/10.1002/(sici)1096-9071(199902)57:2<104::aid-jmv3>3.0.co;2-7" @default.
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