Literature DB >> 14575088

Safety evaluation in chickens of candidate human vaccines against potential pandemic strains of influenza.

Y Matsuoka1, H Chen, N Cox, K Subbarao, J Beck, D Swayne.   

Abstract

Two candidate formalin-inactivated vaccines, made from high-growth reassortant viruses with the HA and NA genes from avian viruses in a background of genes derived from A/Puerto Rico/8/34 (PR8), were prepared against H5N1 and H9N2 subtypes (designated as H5N1/PR8 and H9N2/PR8, respectively). These viruses bear the genotypes, antigenicity, and attenuation in mouse models that are desirable in candidate vaccines. The pathogenicity of the newly generated avian-human reassortant vaccine viruses was also evaluated in chickens. Neither H5N1/PR8 nor H9N2/PR8 were highly pathogenic for chickens. No clinical signs, gross legions, or histological lesions were observed in chickens that were administered H5N1/PR8 either intranasally (i.n.) or intravenously (i.v.), and virus was not detected in oropharyngeal or cloacal swabs. When H9N2/PR8 was administered i.n., no clinical signs, gross lesions, or histological lesions were observed and no virus was detected in cloacal swabs. However, virus was isolated at low titer from oropharyngeal swabs of all eight chickens. Although no clinical signs were observed when H9N2/PR8 was administered i.v., mild tracheitis was seen in one of two chickens. Moderate amounts of antigen were observed in tracheal respiratory epithelium, and low titers of virus were recovered from oropharyngeal and cloacal swabs of some chickens. In summary, both reassortant vaccine viruses replicated poorly in chickens. These studies suggest that these candidate vaccine viruses carry a low risk of transmission to chickens.

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Year:  2003        PMID: 14575088     DOI: 10.1637/0005-2086-47.s3.926

Source DB:  PubMed          Journal:  Avian Dis        ISSN: 0005-2086            Impact factor:   1.577


  8 in total

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Authors:  Teddy John Wohlbold; Ariana Hirsh; Florian Krammer
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2.  Attenuated strains of influenza A viruses do not induce degradation of RNA polymerase II.

Authors:  Ariel Rodriguez; Alicia Pérez-González; M Jaber Hossain; Li-Mei Chen; Thierry Rolling; Pilar Pérez-Breña; Ruben Donis; Georg Kochs; Amelia Nieto
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3.  Cross-reactive mouse monoclonal antibodies raised against the hemagglutinin of A/Shanghai/1/2013 (H7N9) protect against novel H7 virus isolates in the mouse model.

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Journal:  Emerg Microbes Infect       Date:  2018-06-20       Impact factor: 7.163

4.  An In Vitro Microneutralization Assay for Influenza Virus Serology.

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Journal:  Curr Protoc       Date:  2022-07

5.  Safety and immunogenicity of H5N1 influenza vaccine based on baculovirus surface display system of Bombyx mori.

Authors:  Rongzhong Jin; Zhengbing Lv; Qin Chen; Yanping Quan; Haihua Zhang; Si Li; Guogang Chen; Qingliang Zheng; Lairong Jin; Xiangfu Wu; Jianguo Chen; Yaozhou Zhang
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Review 6.  Biosafety risk assessment for production of candidate vaccine viruses to protect humans from zoonotic highly pathogenic avian influenza viruses.

Authors:  Li-Mei Chen; Ruben O Donis; David L Suarez; David E Wentworth; Richard Webby; Othmar G Engelhardt; David E Swayne
Journal:  Influenza Other Respir Viruses       Date:  2019-10-28       Impact factor: 4.380

Review 7.  Pandemic influenza vaccines.

Authors:  Lauren J DiMenna; Hildegund C J Ertl
Journal:  Curr Top Microbiol Immunol       Date:  2009       Impact factor: 4.291

Review 8.  Pre-spillover prevention of emerging zoonotic diseases: what are the targets and what are the tools?

Authors:  J E Childs
Journal:  Curr Top Microbiol Immunol       Date:  2007       Impact factor: 4.291

  8 in total

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