A polyvalent DNA prime with matched polyvalent protein/GLA-SE boost regimen elicited the most robust and broad IgG and IgG3 V1V2 binding antibody and CD4+ T cell responses among 13 HIV vaccine trials

dc.contributor.authorMoodie Z.
dc.contributor.authorLi S.S.
dc.contributor.authorGiorgi E.E.
dc.contributor.authorWilliams L.T.D.
dc.contributor.authorDintwe O.
dc.contributor.authorCarpp L.N.
dc.contributor.authorChen S.
dc.contributor.authorSeaton K.E.
dc.contributor.authorSawant S.S.
dc.contributor.authorZhang L.
dc.contributor.authorHeptinstall J.
dc.contributor.authorLiu S.
dc.contributor.authorGrunenberg N.
dc.contributor.authorTomaka F.
dc.contributor.authorRerks-Ngarm S.
dc.contributor.authorPitisuttithum P.
dc.contributor.authorNitayaphan S.
dc.contributor.authorAke J.A.
dc.contributor.authorVasan S.
dc.contributor.authorPantaleo G.
dc.contributor.authorFrank I.
dc.contributor.authorBaden L.R.
dc.contributor.authorGoepfert P.A.
dc.contributor.authorKeefer M.
dc.contributor.authorChirenje M.
dc.contributor.authorHosseinipour M.C.
dc.contributor.authorMngadi K.
dc.contributor.authorLaher F.
dc.contributor.authorGarrett N.
dc.contributor.authorBekker L.G.
dc.contributor.authorDe Rosa S.
dc.contributor.authorAndersen-Nissen E.
dc.contributor.authorKublin J.G.
dc.contributor.authorLu S.
dc.contributor.authorGilbert P.B.
dc.contributor.authorGray G.E.
dc.contributor.authorCorey L.
dc.contributor.authorMcElrath M.J.
dc.contributor.authorTomaras G.D.
dc.contributor.correspondenceMoodie Z.
dc.contributor.otherMahidol University
dc.date.accessioned2025-04-16T18:29:06Z
dc.date.available2025-04-16T18:29:06Z
dc.date.issued2025-01-01
dc.description.abstractDeveloping an effective HIV vaccine is a momentous challenge. An exceptionally wide range of candidate HIV vaccines have been tested, yet many were poorly immunogenic, and of the select few that advanced into efficacy trials, only one demonstrated any efficacy. Here we report the results of the largest-scale cross-protocol immunogenicity comparison to date: 13 HIV vaccine trials (including 36 vaccine regimens) conducted across nine countries worldwide, strengthened by standardized trial designs, validated assays in centralized laboratories, and harmonized immunogenicity endpoints–providing an objective approach to identify the HIV vaccine candidate(s) with the best immunogenicity. A polyvalent DNA prime + protein boost regimen (HVTN 124) including Env immunogens of four subtypes, matched between prime and boost, achieved the best anti-V1V2 antibody responses by a large margin and also induced high CD4+ T-cell responses–two key immune responses implicated in HIV vaccine protection. Our results provide strong support to test this promising HIV vaccine design in more advanced phase clinical trials and will also guide the future design of additional HIV vaccines. Trial registration:ClinicalTrials.gov identifier: NCT01799954. Trial registration:ClinicalTrials.gov identifier: NCT02109354. Trial registration:ClinicalTrials.gov identifier: NCT02404311. Trial registration:ClinicalTrials.gov identifier: NCT02207920. Trial registration:ClinicalTrials.gov identifier: NCT02296541. Trial registration:ClinicalTrials.gov identifier: NCT03284710. Trial registration:ClinicalTrials.gov identifier: NCT02915016. Trial registration:ClinicalTrials.gov identifier: NCT02997969. Trial registration:ClinicalTrials.gov identifier: NCT03122223. Trial registration:ClinicalTrials.gov identifier: NCT03409276. Trial registration:ClinicalTrials.gov identifier: NCT02968849. Trial registration:ClinicalTrials.gov identifier: NCT03060629. Trial registration:ClinicalTrials.gov identifier: NCT00223080.
dc.identifier.citationEmerging Microbes and Infections Vol.14 No.1 (2025)
dc.identifier.doi10.1080/22221751.2025.2485317
dc.identifier.eissn22221751
dc.identifier.scopus2-s2.0-105002219198
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/123456789/109554
dc.rights.holderSCOPUS
dc.subjectPharmacology, Toxicology and Pharmaceutics
dc.subjectMedicine
dc.subjectImmunology and Microbiology
dc.titleA polyvalent DNA prime with matched polyvalent protein/GLA-SE boost regimen elicited the most robust and broad IgG and IgG3 V1V2 binding antibody and CD4+ T cell responses among 13 HIV vaccine trials
dc.typeArticle
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=105002219198&origin=inward
oaire.citation.issue1
oaire.citation.titleEmerging Microbes and Infections
oaire.citation.volume14
oairecerif.author.affiliationFred Hutchinson Cancer Center
oairecerif.author.affiliationFaculty of Tropical Medicine, Mahidol University
oairecerif.author.affiliationUniversity of the Witwatersrand Faculty of Health Sciences
oairecerif.author.affiliationUNC Project-Malawi
oairecerif.author.affiliationUniversity of Zimbabwe
oairecerif.author.affiliationSouth African Medical Research Council
oairecerif.author.affiliationUniversity of Rochester Medical Center
oairecerif.author.affiliationCentre Hospitalier Universitaire Vaudois
oairecerif.author.affiliationUNC School of Medicine
oairecerif.author.affiliationThe Aurum Institute
oairecerif.author.affiliationBrigham and Women's Hospital
oairecerif.author.affiliationThailand Ministry of Public Health
oairecerif.author.affiliationUniversity of Washington
oairecerif.author.affiliationHJF
oairecerif.author.affiliationWalter Reed Army Institute of Research
oairecerif.author.affiliationJohnson & Johnson
oairecerif.author.affiliationUniversity of KwaZulu-Natal
oairecerif.author.affiliationRoyal Thai Army
oairecerif.author.affiliationDuke University School of Medicine
oairecerif.author.affiliationUAB Department of Medicine
oairecerif.author.affiliationUniversity of Pennsylvania Perelman School of Medicine
oairecerif.author.affiliationUniversity of Massachusetts Chan Medical School
oairecerif.author.affiliationUniversity of Cape Town
oairecerif.author.affiliationWorcester HIV Vaccine
oairecerif.author.affiliationCape Town

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