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 in | Antiviral research Vol. 104; pp. 110 - 117 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Elsevier B.V
01.04.2014
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ISSN | 0166-3542 1872-9096 1872-9096 |
DOI | 10.1016/j.antiviral.2014.01.022 |
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Abstract | •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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AbstractList | 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. •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. 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.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. |
Author | Liu, Shuzhen Bian, Chengrong Gu, Hongjing Zhang, Peirui Li, Zhiwei Wang, Xiliang Xing, Li Zhou, Ya Zhang, Guangzhou Liu, Na Song, Yingwei Yang, Penghui Duan, Yueqiang Wang, Zhaohai Zhang, Keming Zhang, Shaogeng |
Author_xml | – sequence: 1 givenname: Chengrong surname: Bian fullname: Bian, Chengrong organization: Beijing Institute of Microbiology and Epidemiology, State Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China – sequence: 2 givenname: Shuzhen surname: Liu fullname: Liu, Shuzhen organization: National Institutes for Food and Drug Control, Beijing 100050, China – sequence: 3 givenname: Na surname: Liu fullname: Liu, Na organization: Beijing Institute of Microbiology and Epidemiology, State Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China – sequence: 4 givenname: Guangzhou surname: Zhang fullname: Zhang, Guangzhou organization: Laboratory Animal Center of the Academy of Military and Medical Sciences, Beijing 100071, China – sequence: 5 givenname: Li surname: Xing fullname: Xing, Li organization: Beijing Institute of Microbiology and Epidemiology, State Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China – sequence: 6 givenname: Yingwei surname: Song fullname: Song, Yingwei organization: Department of Blood Transfusion, Chinese PLA General Hospital, Beijing 100853, China – sequence: 7 givenname: Yueqiang surname: Duan fullname: Duan, Yueqiang organization: Beijing Institute of Microbiology and Epidemiology, State Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China – sequence: 8 givenname: Hongjing surname: Gu fullname: Gu, Hongjing organization: Beijing Institute of Microbiology and Epidemiology, State Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China – sequence: 9 givenname: Ya surname: Zhou fullname: Zhou, Ya organization: Department of Pathogenic Biology and Medical Immunology, School of Basic Medical Sciences, Ningxia Medical University, Yinchuan 750004, China – sequence: 10 givenname: Peirui surname: Zhang fullname: Zhang, Peirui organization: Department of Hepatobiliary, 302 Military Hospital, Beijing 100039, China – sequence: 11 givenname: Zhiwei surname: Li fullname: Li, Zhiwei organization: Department of Hepatobiliary, 302 Military Hospital, Beijing 100039, China – sequence: 12 givenname: Keming surname: Zhang fullname: Zhang, Keming organization: Department of Hepatobiliary, 302 Military Hospital, Beijing 100039, China – sequence: 13 givenname: Zhaohai surname: Wang fullname: Wang, Zhaohai organization: Department of Hepatobiliary, 302 Military Hospital, Beijing 100039, China – sequence: 14 givenname: Shaogeng surname: Zhang fullname: Zhang, Shaogeng email: zhangsg302@hotmail.com organization: Department of Hepatobiliary, 302 Military Hospital, Beijing 100039, China – sequence: 15 givenname: Xiliang surname: Wang fullname: Wang, Xiliang email: xiliangw@126.com organization: Beijing Institute of Microbiology and Epidemiology, State Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China – sequence: 16 givenname: Penghui surname: Yang fullname: Yang, Penghui email: ypenghuiamms@hotmail.com organization: Beijing Institute of Microbiology and Epidemiology, State Key Laboratory of Pathogen and Biosecurity, Beijing 100071, China |
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Keywords | Fusion and attachment protein epitopes RSV Viral vector Influenza virus Human respiratory syncytial virus Antigenic determinant Orthomyxoviridae Paramyxoviridae Prevention Respiratory tract Pneumovirus Fusion protein Vector Pneumovirinae Antibody Rodentia Vaccine Influenzavirus Virus Immunoprophylaxis Mononegavirales Vertebrata Mammalia Mouse Animal |
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Snippet | •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... Respiratory syncytial virus (RSV) is an important viral pathogen that causes life-threatening respiratory infections in both infants and the elderly; no... |
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SubjectTerms | Animals Antibiotics. Antiinfectious agents. Antiparasitic agents Antibodies, Viral - immunology Antiviral agents Biological and medical sciences Cell Line Cercopithecus aethiops Disease Models, Animal Dogs Epitopes - chemistry Epitopes - immunology Female Fusion and attachment protein epitopes Gene Order Genetic Vectors - genetics Human viral diseases Immunity, Mucosal Immunization Infectious diseases Influenza Vaccines - genetics Influenza Vaccines - immunology Influenza virus Liver - immunology Liver - virology Lung - immunology Lung - pathology Lung - virology Medical sciences Mice Mice, Inbred BALB C Pharmacology. Drug treatments Respiratory Syncytial Virus Infections - immunology Respiratory Syncytial Virus Infections - prevention & control Respiratory Syncytial Viruses - genetics Respiratory Syncytial Viruses - immunology RSV Th1 Cells - immunology Viral diseases Viral diseases of the respiratory system and ent viral diseases Viral Fusion Proteins - genetics Viral Fusion Proteins - immunology Viral vector |
Title | Influenza virus vaccine expressing fusion and attachment protein epitopes of respiratory syncytial virus induces protective antibodies in BALB/c mice |
URI | https://dx.doi.org/10.1016/j.antiviral.2014.01.022 https://www.ncbi.nlm.nih.gov/pubmed/24509239 https://www.proquest.com/docview/1504732250 |
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