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A Zika Vaccine Generated Using the Chimeric Insect-Specific Binjari Virus Platform Protects against Fetal Brain Infection in Pregnant Mice.
Hazlewood, Jessamine E; Rawle, Daniel J; Tang, Bing; Yan, Kexin; Vet, Laura J; Nakayama, Eri; Hobson-Peters, Jody; Hall, Roy A; Suhrbier, Andreas.
Afiliação
  • Hazlewood JE; Inflammation Biology Group, QIMR Berghofer Medical Research Institute, Brisbane, QLD 4006, Australia.
  • Rawle DJ; Inflammation Biology Group, QIMR Berghofer Medical Research Institute, Brisbane, QLD 4006, Australia.
  • Tang B; Inflammation Biology Group, QIMR Berghofer Medical Research Institute, Brisbane, QLD 4006, Australia.
  • Yan K; Inflammation Biology Group, QIMR Berghofer Medical Research Institute, Brisbane, QLD 4006, Australia.
  • Vet LJ; School of Chemistry and Molecular Biosciences, University of Queensland, St. Lucia, QLD 4072, Australia.
  • Nakayama E; Department of Virology I, National Institute of Infectious Diseases, Tokyo 162-0052, Japan.
  • Hobson-Peters J; School of Chemistry and Molecular Biosciences, University of Queensland, St. Lucia, QLD 4072, Australia.
  • Hall RA; Australian Infectious Diseases Research Centre, Brisbane, QLD 4006, Australia.
  • Suhrbier A; School of Chemistry and Molecular Biosciences, University of Queensland, St. Lucia, QLD 4072, Australia.
Vaccines (Basel) ; 8(3)2020 Sep 02.
Article em En | MEDLINE | ID: mdl-32887302
ABSTRACT
Zika virus (ZIKV) is the etiological agent of congenital Zika syndrome (CZS), a spectrum of birth defects that can lead to life-long disabilities. A range of vaccines are in development with the target population including pregnant women and women of child-bearing age. Using a recently described chimeric flavivirus vaccine technology based on the novel insect-specific Binjari virus (BinJV), we generated a ZIKV vaccine (BinJ/ZIKA-prME) and illustrate herein its ability to protect against fetal brain infection. Female IFNAR-/- mice were vaccinated once with unadjuvanted BinJ/ZIKA-prME, were mated, and at embryonic day 12.5 were challenged with ZIKVPRVABC59. No infectious ZIKV was detected in maternal blood, placenta, or fetal heads in BinJ/ZIKA-prME-vaccinated mice. A similar result was obtained when the more sensitive qRT PCR methodology was used to measure the viral RNA. BinJ/ZIKA-prME vaccination also did not result in antibody-dependent enhancement of dengue virus infection or disease. BinJ/ZIKA-prME thus emerges as a potential vaccine candidate for the prevention of CSZ.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Vaccines (Basel) Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Austrália

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: Vaccines (Basel) Ano de publicação: 2020 Tipo de documento: Article País de afiliação: Austrália