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The Perennial Use of the Green Fluorescent Protein Marker in a Live Vaccinia Virus Ankara Recombinant Platform Shows No Acute Adverse Effects in Mice.
Daian E Silva, D S O; Pinho, T M G; Rachid, M A; Barbosa-Stancioli, D F; Da Fonseca, F G.
Afiliação
  • Daian E Silva DSO; Laboratory of Basic and Applied Virology, Departmento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
  • Pinho TMG; Laboratory of Basic and Applied Virology, Departmento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
  • Rachid MA; Departamento de Patologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
  • Barbosa-Stancioli DF; Laboratory of Basic and Applied Virology, Departmento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil.
  • Da Fonseca FG; Laboratory of Basic and Applied Virology, Departmento de Microbiologia, Instituto de Ciências Biológicas, Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil. fdafonseca@icb.ufmg.br.
Braz J Microbiol ; 50(2): 347-355, 2019 Apr.
Article em En | MEDLINE | ID: mdl-30877662
Recombinant virus vectors represent a promising strategy for vaccine research. Among available viral vectors, members of the Poxviridae family-especially the modified Vaccinia virus Ankara (MVA)-stand out as immunogenic and safe vaccine platforms. Because MVA usually does not produce plaques in cell culture, visible selection markers such as the green fluorescent protein (GFP) are frequently incorporated into the constructions in order to facilitate the recognition of recombinants. However, these genetic markers have to be removed before any clinical trial. Here, we evaluated the acute responses generated in mice immunized with a MVA vector in which the GFP marker was not removed. We observed no differences in neutrophil, monocyte, or total leucocyte recruitment among animals inoculated with MVA or MVA-GFP. Likewise, there were no differences in neutrophil activation between mice groups. Hepatic functions were not altered in either MVA or MVA-GFP-inoculated mice, and we observed no histopathological alterations in different tissues from virus-inoculated animals. In conclusion, the presence of GFP is innocuous to immunized animals and do not alter acute physiopathological responses to the MVA vector. We suggest that keeping the GFP marker may be a good strategy for vaccine development, production, and evaluation.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vaccinia virus / Vacinas Atenuadas / Vacinas Virais / Proteínas de Fluorescência Verde Limite: Animals Idioma: En Revista: Braz J Microbiol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Brasil País de publicação: Brasil

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Vaccinia virus / Vacinas Atenuadas / Vacinas Virais / Proteínas de Fluorescência Verde Limite: Animals Idioma: En Revista: Braz J Microbiol Ano de publicação: 2019 Tipo de documento: Article País de afiliação: Brasil País de publicação: Brasil