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Bivalent vaccine platform based on ca influenza virus vaccine elicits protective immunity against human adenoviruses.
Gu, Hongjing; Gao, Yaqian; Zhou, Shanshan; Sun, Fang; Zhao, Zhongpeng; Wang, Keyu; Zhao, Lingna; Zhang, Peirui; Wang, Zhaohai; Zhang, Shaogeng; Wang, Xiliang; Yang, Penghui.
Afiliação
  • Gu H; Beijing Institute of Microbiology and Epidemiology, State Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China.
  • Gao Y; Beijing Institute of Microbiology and Epidemiology, State Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China.
  • Zhou S; Beijing Institute of Microbiology and Epidemiology, State Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China.
  • Sun F; Beijing 302 Hospital, Beijing 100039, China.
  • Zhao Z; Beijing Institute of Microbiology and Epidemiology, State Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China.
  • Wang K; Beijing Institute of Microbiology and Epidemiology, State Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China.
  • Zhao L; Beijing Institute of Microbiology and Epidemiology, State Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China.
  • Zhang P; Beijing 302 Hospital, Beijing 100039, China.
  • Wang Z; Beijing 302 Hospital, Beijing 100039, China.
  • Zhang S; Beijing 302 Hospital, Beijing 100039, China.
  • Wang X; Beijing Institute of Microbiology and Epidemiology, State Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China. Electronic address: xiliangw@126.com.
  • Yang P; Beijing Institute of Microbiology and Epidemiology, State Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China; Beijing 302 Hospital, Beijing 100039, China. Electronic address: ypenghuiamms@hotmail.com.
Antiviral Res ; 153: 78-84, 2018 05.
Article em En | MEDLINE | ID: mdl-29501624
ABSTRACT
Human adenoviruses (HAdVs) are prevalent in pediatric and adult patients with severe acute respiratory disease (ARD). To date, there have been no widely used HAdV vaccines available. In this report, we developed a cold-adapted attenuated influenza virus, termed rg HAdV-Flu ca, carrying epitopes from HAdV hexon protein in the backbone of the ca influenza vaccine neuraminidase (NA) gene using reverse genetics. Rg HAdV-Flu ca virus exhibited a cold-adapted (ca) phenotype, and its morphological characteristics were observed using electron microscopy. Moreover, BALB/c mice were immunized intranasally (i.n.) with 105, 106 or 107 TCID50 rg HAdV-Flu ca. Results showed a specific, robust antibody response against influenza and HAdV in a dose-dependent manner. More importantly, potent humoral, mucosal and cellular immune responses protected against subsequent wild-type HAdV-3 or HAdV-7 challenges, as determined by a significant decrease in viral titers and a noticeable alleviation of histopathological alterations in the lung tissue of challenged mice. These findings demonstrate that rg HAdV-Flu ca warrants attention as a potential vaccine candidate against HAdV infection.
Assuntos

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Assunto principal: Orthomyxoviridae / Vacinas contra Influenza / Adenovírus Humanos Limite: Animals Idioma: En Revista: Antiviral Res Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Contexto em Saúde: 1_ASSA2030 Base de dados: MEDLINE Assunto principal: Orthomyxoviridae / Vacinas contra Influenza / Adenovírus Humanos Limite: Animals Idioma: En Revista: Antiviral Res Ano de publicação: 2018 Tipo de documento: Article