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

Show simple item record

dc.contributor.author Fellows, Tamika
dc.contributor.author Page, Nicola Anne
dc.contributor.author Fix, Alan
dc.contributor.author Flores, Jorge
dc.contributor.author Cryz, Stanley
dc.contributor.author McNeal, Monica
dc.contributor.author Iturriza-Gomara, Miren
dc.contributor.author Groome, Michelle J.
dc.date.accessioned 2023-11-30T10:53:31Z
dc.date.available 2023-11-30T10:53:31Z
dc.date.issued 2023-08-25
dc.description SUPPLEMENTARY 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.description DATA 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.abstract A 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.department Medical Virology en_US
dc.description.librarian am2023 en_US
dc.description.sdg SDG-03:Good heatlh and well-being en_US
dc.description.sponsorship The Bill and Melinda Gates Foundation. en_US
dc.description.uri https://www.mdpi.com/journal/viruses en_US
dc.identifier.citation Fellows, 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.issn 1999-4915 (online)
dc.identifier.other 10.3390/v15091809
dc.identifier.uri http://hdl.handle.net/2263/93564
dc.language.iso en en_US
dc.publisher MDPI en_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.subject Rotavirus vaccine en_US
dc.subject Immune response en_US
dc.subject Pediatric en_US
dc.subject Fecal shedding en_US
dc.subject Oral rotavirus vaccine (ORV) en_US
dc.subject SDG-03: Good health and well-being en_US
dc.title 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 en_US
dc.type Article en_US


Files in this item

This item appears in the following Collection(s)

Show simple item record