Influenza virus vaccine expressing fusion and attachment protein epitopes of respiratory syncytial virus induces protective antibodies in BALB/c mice

•A recombinant influenza virus rFlu/RSV/F+G containing RSV F and G protein epitopes was generated.•rFlu/RSV/F+G showed specific antibody response against influenza virus and RSV in mice.•rFlu/RSV/F+G might elicit Th1-type cellular immune response against RSV.•rFlu/RSV/F+G could induce immune protect...

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Published inAntiviral research Vol. 104; pp. 110 - 117
Main Authors Bian, Chengrong, Liu, Shuzhen, Liu, Na, Zhang, Guangzhou, Xing, Li, Song, Yingwei, Duan, Yueqiang, Gu, Hongjing, Zhou, Ya, Zhang, Peirui, Li, Zhiwei, Zhang, Keming, Wang, Zhaohai, Zhang, Shaogeng, Wang, Xiliang, Yang, Penghui
Format Journal Article
LanguageEnglish
Published Kidlington Elsevier B.V 01.04.2014
Elsevier
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Summary:•A recombinant influenza virus rFlu/RSV/F+G containing RSV F and G protein epitopes was generated.•rFlu/RSV/F+G showed specific antibody response against influenza virus and RSV in mice.•rFlu/RSV/F+G might elicit Th1-type cellular immune response against RSV.•rFlu/RSV/F+G could induce immune protective effect against influenza virus and RSV. Respiratory syncytial virus (RSV) is an important viral pathogen that causes life-threatening respiratory infections in both infants and the elderly; no vaccines are at present available. In this report, we examined the use of influenza virus as a vehicle for production of an experimental RSV vaccine. We used reverse genetics to generate a recombinant influenza A virus with epitopes from the RSV fusion (F) and attachment (G) proteins (rFlu/RSV/F+G) in the influenza virus nonstructural (NS1) protein gene. Expression of RSV F+G epitope proteins was confirmed by Western blotting, and no changes in viral morphology were evident following examination by electron microscopy. BALB/c mice immunized intranasally with rFlu/RSV/F+G showed viral-specific antibody responses against both influenza and RSV. Total IgG, IgG1, IgG2a and IgA were measured in mice immunized with rFlu/RSV/F+G, revealing robust cellular and mucosal immune responses. Furthermore, we found that rFlu/RSV/F+G conferred protection against subsequent influenza and RSV challenges, showing significant decreases in viral replication and obvious attenuation of histopathological changes associated with viral infections. These findings suggest that rFlu/RSV/F+G is a promising vaccine candidate, which should be further assessed using cotton rat and primate models.
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ISSN:0166-3542
1872-9096
1872-9096
DOI:10.1016/j.antiviral.2014.01.022