| Literature DB >> 28374245 |
Vincent Pavot1, Sarah Sebastian1, Alison V Turner1, Jake Matthews1, Sarah C Gilbert2.
Abstract
The smallpox vaccine based on the vaccinia virus was successfully used to eradicate smallpox, but although very effective, it was a very reactogenic vaccine and responsible for the deaths of one to two people per million vaccinated. Modified Vaccinia virus Ankara (MVA) is an attenuated derivative, also used in the smallpox eradication campaign and now being developed as a recombinant viral vector to produce vaccines against infectious diseases and cancer. MVA can encode one or more foreign antigens and thus can function as a multivalent vaccine. The vector can be used at biosafety level 1, has intrinsic adjuvant properties, and induces humoral and cellular immune responses. Many clinical trials of these new vaccines have been conducted, and the safety of MVA is now well documented. Immunogenicity is influenced by the dose and vaccination regimen, and information on the efficacy of MVA-vectored vaccines is now beginning to accumulate. In this chapter, we provide protocols for generation, isolation, amplification, and purification of recombinant MVA for preclinical and clinical evaluation.Entities:
Keywords: Clinical trials; Large-scale production; Modified vaccinia virus Ankara; Non-replicative viral vector; Recombinant vaccines
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Year: 2017 PMID: 28374245 DOI: 10.1007/978-1-4939-6869-5_6
Source DB: PubMed Journal: Methods Mol Biol ISSN: 1064-3745