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Combined Live Oral Priming and Intramuscular Boosting Regimen with Rotarix® and a Nanoparticle-Based Trivalent Rotavirus Vaccine Evaluated in Gnotobiotic Pig Models of G4P[6] and G1P[8] Human Rotavirus Infection

dc.contributor.authorHensley, Caseyen
dc.contributor.authorNyblade, Charlotteen
dc.contributor.authorZhou, Pengen
dc.contributor.authorParreño, Vivianaen
dc.contributor.authorRamesh, Ashwinen
dc.contributor.authorFrazier, Annieen
dc.contributor.authorFrazier, Maggieen
dc.contributor.authorGarrison, Sarahen
dc.contributor.authorFantasia-Davis, Arianaen
dc.contributor.authorCai, Ruiqingen
dc.contributor.authorHuang, Peng-Weien
dc.contributor.authorXia, Mingen
dc.contributor.authorTan, Mingen
dc.contributor.authorYuan, Lijuanen
dc.date.accessioned2023-05-15T13:42:34Zen
dc.date.available2023-05-15T13:42:34Zen
dc.date.issued2023-05-02en
dc.date.updated2023-05-12T12:36:26Zen
dc.description.abstractHuman rotavirus (HRV) is the causative agent of severe dehydrating diarrhea in children under the age of five, resulting in up to 215,000 deaths each year. These deaths almost exclusively occur in low- and middle-income countries where vaccine efficacy is the lowest due to chronic malnutrition, gut dysbiosis, and concurrent enteric viral infection. Parenteral vaccines for HRV are particularly attractive as they avoid many of the concerns associated with currently used live oral vaccines. In this study, a two-dose intramuscular (IM) regimen of the trivalent, nanoparticle-based, nonreplicating HRV vaccine (trivalent S<sub>60</sub>-VP8*), utilizing the shell (S) domain of the capsid of norovirus as an HRV VP8* antigen display platform, was evaluated for immunogenicity and protective efficacy against P[6] and P[8] HRV using gnotobiotic pig models. A prime&ndash;boost strategy using one dose of the oral Rotarix<sup>&reg;</sup> vaccine, followed by one dose of the IM trivalent nanoparticle vaccine was also evaluated. Both regimens were highly immunogenic in inducing serum virus neutralizing, IgG, and IgA antibodies. The two vaccine regimens failed to confer significant protection against diarrhea; however, the prime&ndash;boost regimen significantly shortened the duration of virus shedding in pigs challenged orally with the virulent Wa (G1P[8]) HRV and significantly shortened the mean duration of virus shedding, mean peak titer, and area under the curve of virus shedding after challenge with Arg (G4P[6]) HRV. Prime&ndash;boost-vaccinated pigs challenged with P[8] HRV had significantly higher P[8]-specific IgG antibody-secreting cells (ASCs) in the spleen post-challenge. Prime&ndash;boost-vaccinated pigs challenged with P[6] HRV had significantly higher numbers of P[6]- and P[8]-specific IgG ASCs in the ileum, as well as significantly higher numbers of P[8]-specific IgA ASCs in the spleen post-challenge. These results suggest the promise of and warrant further investigation into the oral priming and parenteral boosting strategy for future HRV vaccines.en
dc.description.versionPublished versionen
dc.format.mimetypeapplication/pdfen
dc.identifier.citationHensley, C.; Nyblade, C.; Zhou, P.; Parreño, V.; Ramesh, A.; Frazier, A.; Frazier, M.; Garrison, S.; Fantasia-Davis, A.; Cai, R.; Huang, P.-W.; Xia, M.; Tan, M.; Yuan, L. Combined Live Oral Priming and Intramuscular Boosting Regimen with Rotarix® and a Nanoparticle-Based Trivalent Rotavirus Vaccine Evaluated in Gnotobiotic Pig Models of G4P[6] and G1P[8] Human Rotavirus Infection. Vaccines 2023, 11, 927.en
dc.identifier.doihttps://doi.org/10.3390/vaccines11050927en
dc.identifier.urihttp://hdl.handle.net/10919/115034en
dc.language.isoenen
dc.publisherMDPIen
dc.rightsCreative Commons Attribution 4.0 Internationalen
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/en
dc.subjectrotavirus nanoparticleen
dc.subjectgnotobiotic pigen
dc.subjectpriming immunizationen
dc.titleCombined Live Oral Priming and Intramuscular Boosting Regimen with Rotarix® and a Nanoparticle-Based Trivalent Rotavirus Vaccine Evaluated in Gnotobiotic Pig Models of G4P[6] and G1P[8] Human Rotavirus Infectionen
dc.title.serialVaccinesen
dc.typeArticle - Refereeden
dc.type.dcmitypeTexten

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