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Simian Adenoviruses As Vaccine Vectors
Author(s) -
Susan Morris,
Sarah Sebastian,
Alexandra J. Spencer,
Sarah C. Gilbert
Publication year - 2016
Publication title -
future virology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.462
H-Index - 34
eISSN - 1746-0808
pISSN - 1746-0794
DOI - 10.2217/fvl-2016-0070
Subject(s) - virology , immunogenicity , tropism , simian , vector (molecular biology) , biology , viral vector , tissue tropism , serotype , population , immune system , antigen , virus , immunology , medicine , gene , recombinant dna , genetics , environmental health
Replication incompetent human adenovirus serotype 5 (HAdV-C5) has been extensively used as a delivery vehicle for gene therapy proteins and infectious disease antigens. These vectors infect replicating and nonreplicating cells, have a broad tissue tropism, elicit high immune responses and are easily purified to high titers. However, the utility of HAdV-C5 vectors as potential vaccines is limited due to pre-existing immunity within the human population that significantly reduces the immunogenicity of HAdV-C5 vaccines. In recent years, adenovirus vaccine development has focused on simian-derived adenoviral vectors, which have the desirable vector characteristics of HAdV-C5 but with negligible seroprevalence in the human population. Here, we discuss recent advances in simian adenovirus vaccine vector development and evaluate current research specifically focusing on clinical trial data.

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