Association between immunogenicity of a monovalent parenteral P2-VP8 subunit rotavirus vaccine and fecal shedding of rotavirus following Rotarix challenge during a randomized, double-blind, placebo-controlled trial

dc.contributor.authorFellows, Tamika
dc.contributor.authorPage, Nicola Anne
dc.contributor.authorFix, Alan
dc.contributor.authorFlores, Jorge
dc.contributor.authorCryz, Stanley
dc.contributor.authorMcNeal, Monica
dc.contributor.authorIturriza-Gomara, Miren
dc.contributor.authorGroome, Michelle J.
dc.date.accessioned2023-11-30T10:53:31Z
dc.date.available2023-11-30T10:53:31Z
dc.date.issued2023-08-25
dc.descriptionSUPPLEMENTARY MATERIALS : TABLE S1: Baseline demographic and clinical factors between rotavirus shedders and non-shedders, as determined by ELISA, stratified by vaccination status: three injections of P2-VP8-P[8] vaccine (30 g and 60 g doses; n = 91) or placebo (n = 44); FIGURE S1: Schedule of events for infants.en_US
dc.descriptionDATA AVAILABILITY STATEMENT : The data presented in this study are available on request from the corresponding author. The data are not publicly available due to a clinical trial agreement with PATH Vaccine Solutions.en_US
dc.description.abstractA correlate of protection for rotavirus (RV) has not been consistently identified. Shedding of RV following an oral rotavirus vaccine (ORV) challenge has been investigated as a potential model to assess protection of parenteral RV vaccines. We previously showed that shedding of a challenge ORV dose was significantly reduced among recipients of a parenteral monovalent RV subunit vaccine (P2-VP8-P[8]) compared to placebo recipients. This secondary data analysis assessed the association between fecal shedding of RV, as determined by ELISA one week after receipt of a Rotarix challenge dose at 18 weeks of age, and serum RV-specific antibody responses, one and six months after vaccination with the third dose of the P2-VP8-P[8] vaccine or placebo. We did not find any association between serum RV-specific immune responses measured one month post-P2-VP8-P[8] vaccination and fecal shedding of RV post-challenge. At nine months of age, six months after the third P2-VP8-P[8] or placebo injection and having received three doses of Rotarix, infants shedding RV demonstrated higher immune responses than non-shedders, showing that RV shedding is reflective of vaccine response following ORV. Further evaluation is needed in a larger sample before fecal shedding of an ORV challenge can be used as a measure of field efficacy in RV vaccine trials.en_US
dc.description.departmentMedical Virologyen_US
dc.description.librarianam2023en_US
dc.description.sdgSDG-03:Good heatlh and well-beingen_US
dc.description.sponsorshipThe Bill and Melinda Gates Foundation.en_US
dc.description.urihttps://www.mdpi.com/journal/virusesen_US
dc.identifier.citationFellows, T.; Page, N.; Fix, A.; Flores, J.; Cryz, S.; McNeal, M.; Iturriza-Gomara, M.; Groome, M.J. Association between Immunogenicity of a Monovalent Parenteral P2-VP8 Subunit Rotavirus Vaccine and Fecal Shedding of Rotavirus following Rotarix Challenge during a Randomized, Double-Blind, Placebo-Controlled Trial. Viruses 2023, 15, 1809. https://DOI.org/10.3390/v15091809.en_US
dc.identifier.issn1999-4915 (online)
dc.identifier.other10.3390/v15091809
dc.identifier.urihttp://hdl.handle.net/2263/93564
dc.language.isoenen_US
dc.publisherMDPIen_US
dc.rights© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license.en_US
dc.subjectRotavirus vaccineen_US
dc.subjectImmune responseen_US
dc.subjectPediatricen_US
dc.subjectFecal sheddingen_US
dc.subjectOral rotavirus vaccine (ORV)en_US
dc.subjectSDG-03: Good health and well-beingen_US
dc.titleAssociation between immunogenicity of a monovalent parenteral P2-VP8 subunit rotavirus vaccine and fecal shedding of rotavirus following Rotarix challenge during a randomized, double-blind, placebo-controlled trialen_US
dc.typeArticleen_US

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