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Immunogenicity and efficacy testing in chimpanzees of an oral hepatitis B vaccine based on live recombinant adenovirus.

机译:基于活重组腺病毒的口服乙型肝炎疫苗的黑猩猩的免疫原性和功效测试。

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摘要

As a major cause of acute and chronic liver disease as well as hepatocellular carcinoma, hepatitis B virus (HBV) continues to pose significant health problems world-wide. Recombinant hepatitis B vaccines based on adenovirus vectors have been developed to address global needs for effective control of hepatitis B infection. Although considerable progress has been made in the construction of recombinant adenoviruses that express large amounts of HBV gene products, preclinical immunogenicity and efficacy testing of candidate vaccines has remained difficult due to the lack of a suitable animal model. We demonstrate here that chimpanzees are susceptible to enteric infection by human adenoviruses type 7 (Ad7) and type 4 (Ad4) following oral administration of live virus. Moreover, after sequential oral immunization with Ad7- and Ad4-vectored vaccines containing the hepatitis B surface antigen (HBsAg) gene, significant antibody responses to HBsAg (anti-HBs) were induced in two chimpanzees. After challenge with heterologous HBV, one chimpanzee was protected from acute hepatitis and the other chimpanzee experienced modified HBV-induced disease. These data demonstrate the feasibility of using orally administered recombinant adenoviruses as a general approach to vaccination.
机译:作为急,慢性肝病以及肝细胞癌的主要原因,乙型肝炎病毒(HBV)继续在全球范围内构成严重的健康问题。已经开发出基于腺病毒载体的重组乙型肝炎疫苗,以满足有效控制乙型肝炎感染的全球需求。尽管在表达大量HBV基因产物的重组腺病毒的构建方面已经取得了很大的进展,但是由于缺乏合适的动物模型,候选疫苗的临床前免疫原性和功效测试仍然很困难。我们在这里证明黑猩猩在口服活病毒后易受人类7型腺病毒(Ad7)和4型腺病毒(Ad4)肠道感染。此外,在用含有乙型肝炎表面抗原(HBsAg)基因的Ad7和Ad4载体疫苗进行顺序口服免疫后,在两只黑猩猩中诱导了对HBsAg的显着抗体反应(抗HBs)。用异源HBV攻击后,一只黑猩猩受到了急性肝炎的保护,而另一只黑猩猩则经历了由HBV引起的改良疾病。这些数据证明了使用口服施用的重组腺病毒作为常规疫苗接种方法的可行性。

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