Cookies on this website
We use cookies to ensure that we give you the best experience on our website. If you click 'Continue' we'll assume that you are happy to receive all cookies and you won't see this message again. Click 'Find out more' for information on how to change your cookie settings.

An E1-deletion-containing adenoviral recombinant based on the chimpanzee serotype 68 (AdC68) was developed to express the rabies virus glycoprotein. Mice immunized with this construct ( developed antibodies to rabies virus and remained resistant to challenge with an otherwise lethal dose of rabies virus. In naïve mice immunized intranasally, the rabies virus-specific antibody responses elicited by were comparable with regard to both titers and isotype profiles to those induced by an adenoviral recombinant based on human serotype 5 (Adhu5) expressing the same transgene product. In contrast, subcutaneous immunization with the vaccine resulted in markedly lower antibody responses to the rabies virus glycoprotein than the corresponding Adhu5 vaccine. Antibodies from mice were strongly biased towards the immunoglobulin G2a isotype. The antibody response to the rabies virus glycoprotein presented by was severely compromised in animals preexposed to the homologous adenovirus. In contrast, the rabies virus-specific antibody response to the vaccine was at most marginally affected by preexisting immunity to common human adenovirus serotypes, such as 2, 4, 5, 7, and 12. This novel vaccine carrier thus offers a distinct advantage over adenoviral vaccines based on common human serotypes.

Original publication




Journal article


J Virol

Publication Date





2667 - 2675


Adenoviruses, Simian, Animals, Antibodies, Viral, Antigens, Viral, B-Lymphocytes, Cell Line, Female, Genetic Vectors, Glycoproteins, Humans, Mice, Mice, Inbred C3H, Rabies, Rabies Vaccines, Rabies virus, Serotyping, Transgenes, Vaccination, Viral Envelope Proteins