Immunogenicity of a recombinant plant-produced respiratory syncytial virus F subunit vaccine in mice

dc.contributor.authorPisuttinusart N.
dc.contributor.authorShanmugaraj B.
dc.contributor.authorSrisaowakarn C.
dc.contributor.authorKetloy C.
dc.contributor.authorPrompetchara E.
dc.contributor.authorThitithanyanont A.
dc.contributor.authorPhoolcharoen W.
dc.contributor.correspondencePisuttinusart N.
dc.contributor.otherMahidol University
dc.date.accessioned2024-02-08T18:11:37Z
dc.date.available2024-02-08T18:11:37Z
dc.date.issued2024-03-01
dc.description.abstractRespiratory syncytial virus (RSV) is a highly infectious respiratory virus that causes serious illness, particularly in young children, elderly people, and those with immunocompromised individuals. RSV infection is the leading cause of infant hospitalization and can lead to serious complications such as pneumonia and bronchiolitis. Currently, there is an RSV vaccine approved exclusively for the elderly population, but no approved vaccine specifically designed for infants or any other age groups. Therefore, it is crucial to continue the development of an RSV vaccine specifically tailored for these populations. In this study, the immunogenicity of the two plant-produced RSV-F Fc fusion proteins (Native construct and structural stabilized construct) were examined to assess them as potential vaccine candidates for RSV. The RSV-F Fc fusion proteins were transiently expressed in Nicotiana benthamiana and purified using protein A affinity column chromatography. The recombinant RSV-F Fc fusion protein was recognized by the monoclonal antibody Motavizumab specific against RSV-F protein. Moreover, the immunogenicity of the two purified RSV-F Fc proteins were evaluated in mice by formulating with different adjuvants. According to our results, the plant-produced RSV-F Fc fusion protein is immunogenic in mice. These preliminary findings, demonstrate the immunogenicity of plant-based RSV-F Fc fusion protein, however, further preclinical studies such as antigen dose and adjuvant optimization, safety, toxicity, and challenge studies in animal models are necessary in order to prove the vaccine efficacy.
dc.identifier.citationBiotechnology Reports Vol.41 (2024)
dc.identifier.doi10.1016/j.btre.2023.e00826
dc.identifier.eissn2215017X
dc.identifier.scopus2-s2.0-85181833811
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/95700
dc.rights.holderSCOPUS
dc.subjectBiochemistry, Genetics and Molecular Biology
dc.subjectImmunology and Microbiology
dc.titleImmunogenicity of a recombinant plant-produced respiratory syncytial virus F subunit vaccine in mice
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85181833811&origin=inward
oaire.citation.titleBiotechnology Reports
oaire.citation.volume41
oairecerif.author.affiliationChulalongkorn University
oairecerif.author.affiliationBharathiar University
oairecerif.author.affiliationMahidol University
oairecerif.author.affiliationFaculty of Medicine, Chulalongkorn University
oairecerif.author.affiliationLtd

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