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In vivo hepatitis B virus-neutralizing activity of an anti-HBsAg humanized antibody in chimpanzees

机译:抗HBsAg人源化抗体在黑猩猩中的体内乙肝病毒中和活​​性

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摘要

Previously, we constructed a humanized antibody (HuS10) that binds to the common a antigenic determinant on the S protein of HBV. In this study, we evaluated its HBV-neutralizing activity in chimpanzees. A study chimpanzee was intravenously administered with a single dose of HuS10, followed by intravenous challenge with the adr subtype of HBV, while a control chimpanzee was only challenged with the virus. The result showed that the control chimpanzee was infected by the virus, and thus serum HBV surface antigen (HBsAg) became positive from the 14th to 20th week and actively acquired serum anti-HBc and anti-HBs antibodies appeared from the 19th and 23rd week, respectively. However, in the case of the study chimpanzee, serum HBsAg became positive from the 34th to 37th week, while actively acquired serum anti-HBc and anti-HBs antibodies appeared from the 37th and 40th week, respectively, indicating that HuS10 neutralized the virus in vivo and thus delayed the HBV infection. This novel humanized antibody will be useful in the immunoprophylaxis of HBV infection.
机译:以前,我们构建了一种人源化抗体(HuS10),该抗体与常见的HBV S蛋白抗原决定簇结合。在这项研究中,我们评估了它在黑猩猩中的HBV中和活性。一只研究黑猩猩静脉内注射单剂量的HuS10,然后用HBV的adr亚型进行静脉内攻击,而对照黑猩猩只用该病毒攻击。结果表明,对照黑猩猩感染了该病毒,因此从第14周到第20周,血清HBV表面抗原(HBsAg)变为阳性,并在第19周和第23周出现了主动获得的血清抗HBc和抗HBs抗体,分别。然而,在研究黑猩猩的情况下,血清HBsAg从第34周到第37周变为阳性,而主动获得的血清抗HBc和抗HBs抗体分别从第37周和第40周出现,表明HuS10中和了该病毒。体内因而延迟了HBV感染。这种新型的人源化抗体可用于HBV感染的免疫预防。

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