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Hazard Characterization of Modified Vaccinia Virus Ankara Vector: What Are the Knowledge Gaps?
Okeke, Malachy I; Okoli, Arinze S; Diaz, Diana; Offor, Collins; Oludotun, Taiwo G; Tryland, Morten; Bøhn, Thomas; Moens, Ugo.
Affiliation
  • Okeke MI; Genome Editing Research Group, GenØk-Center for Biosafety, Siva Innovation Center, N-9294 Tromso, Norway. malachy.okeke@uit.no.
  • Okoli AS; Genome Editing Research Group, GenØk-Center for Biosafety, Siva Innovation Center, N-9294 Tromso, Norway. arinze.s.okoli@uit.no.
  • Diaz D; Molecular Inflammation Research Group, Institute of Medical Biology, University i Tromsø (UiT)-The Arctic University of Norway, N-9037 Tromso, Norway. diana.k.canova@uit.no.
  • Offor C; Department of Medical and Pharmaceutical Biotechnology, IMC University of Applied Sciences Piaristengasse 1, A-3500 Krems, Austria. collinsoffor57@yahoo.com.
  • Oludotun TG; Department of Medical and Pharmaceutical Biotechnology, IMC University of Applied Sciences Piaristengasse 1, A-3500 Krems, Austria. graceoludotun@yahoo.com.
  • Tryland M; Genome Editing Research Group, GenØk-Center for Biosafety, Siva Innovation Center, N-9294 Tromso, Norway. morten.tryland@uit.no.
  • Bøhn T; Artic Infection Biology, Department of Artic and Marine Biology, UIT-The Artic University of Norway, N-9037 Tromso, Norway. morten.tryland@uit.no.
  • Moens U; Genome Editing Research Group, GenØk-Center for Biosafety, Siva Innovation Center, N-9294 Tromso, Norway. thomas.bohn@uit.no.
Viruses ; 9(11)2017 10 29.
Article in En | MEDLINE | ID: mdl-29109380
ABSTRACT
Modified vaccinia virus Ankara (MVA) is the vector of choice for human and veterinary applications due to its strong safety profile and immunogenicity in vivo. The use of MVA and MVA-vectored vaccines against human and animal diseases must comply with regulatory requirements as they pertain to environmental risk assessment, particularly the characterization of potential adverse effects to humans, animals and the environment. MVA and recombinant MVA are widely believed to pose low or negligible risk to ecosystem health. However, key aspects of MVA biology require further research in order to provide data needed to evaluate the potential risks that may occur due to the use of MVA and MVA-vectored vaccines. The purpose of this paper is to identify knowledge gaps in the biology of MVA and recombinant MVA that are of relevance to its hazard characterization and discuss ongoing and future experiments aimed at providing data necessary to fill in the knowledge gaps. In addition, we presented arguments for the inclusion of uncertainty analysis and experimental investigation of verifiable worst-case scenarios in the environmental risk assessment of MVA and recombinant MVA. These will contribute to improved risk assessment of MVA and recombinant MVA vaccines.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Vaccinia virus / Vaccines, Synthetic / Genetic Vectors Type of study: Etiology_studies / Risk_factors_studies Limits: Animals / Humans Language: En Journal: Viruses Year: 2017 Document type: Article Affiliation country: Noruega

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Vaccinia virus / Vaccines, Synthetic / Genetic Vectors Type of study: Etiology_studies / Risk_factors_studies Limits: Animals / Humans Language: En Journal: Viruses Year: 2017 Document type: Article Affiliation country: Noruega