Publication:
Antibody to HSV gD peptide induced by vaccination does not protect against HSV-2 infection in HSV-2 seronegative women

dc.contributor.authorPeter B. Gilberten_US
dc.contributor.authorJean Louis Excleren_US
dc.contributor.authorGeorgia D. Tomarasen_US
dc.contributor.authorLindsay N. Carppen_US
dc.contributor.authorBarton F. Haynesen_US
dc.contributor.authorHua Xin Liaoen_US
dc.contributor.authorDavid C. Montefiorien_US
dc.contributor.authorSupachai Rerks-Ngarmen_US
dc.contributor.authorPunnee Pitisuttithumen_US
dc.contributor.authorSorachai Nitayaphanen_US
dc.contributor.authorJaranit Kaewkungwalen_US
dc.contributor.authorGustavo H. Kijaken_US
dc.contributor.authorSodsai Tovanabutraen_US
dc.contributor.authorDonald P. Francisen_US
dc.contributor.authorCarter Leeen_US
dc.contributor.authorFaruk Sinangilen_US
dc.contributor.authorPhillip W. Bermanen_US
dc.contributor.authorNakorn Premsrien_US
dc.contributor.authorPrayura Kunasolen_US
dc.contributor.authorRobert J. O'Connellen_US
dc.contributor.authorNelson L. Michaelen_US
dc.contributor.authorMerlin L. Robben_US
dc.contributor.authorRhoda Morrowen_US
dc.contributor.authorLawrence Coreyen_US
dc.contributor.authorJerome H. Kimen_US
dc.contributor.otherFred Hutchinson Cancer Research Centeren_US
dc.contributor.otherUniversity of Washington, Seattleen_US
dc.contributor.otherHJFen_US
dc.contributor.otherWalter Reed Army Institute of Researchen_US
dc.contributor.otherDuke University School of Medicineen_US
dc.contributor.otherDuke University Medical Centeren_US
dc.contributor.otherThailand Ministry of Public Healthen_US
dc.contributor.otherMahidol Universityen_US
dc.contributor.otherArmed Forces Research Institute of Medical Sciences, Thailanden_US
dc.contributor.otherGlobal Solutions for Infectious Diseasesen_US
dc.contributor.otherUniversity of California, Santa Cruzen_US
dc.contributor.otherInternational Vaccine Initiativeen_US
dc.date.accessioned2018-12-21T06:30:59Z
dc.date.accessioned2019-03-14T08:02:26Z
dc.date.available2018-12-21T06:30:59Z
dc.date.available2019-03-14T08:02:26Z
dc.date.issued2017-05-01en_US
dc.description.abstract© This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication. Background: In the HIV-1 vaccine trial RV144, ALVAC-HIV prime with an AIDSVAX® B/E boost reduced HIV-1 acquisition by 31% at 42 months post first vaccination. The bivalent AIDSVAX ® B/E vaccine contains two gp120 envelope glycoproteins, one from the subtype B HIV-1 MN isolate and one from the subtype CRF01-AE A244 isolate. Each envelope glycoprotein harbors a highly conserved 27-amino acid HSV-1 glycoprotein D (gD) tag sequence that shares 93% sequence identity with the HSV-2 gD sequence. We assessed whether vaccine-induced anti-gD antibodies protected females against HSV-2 acquisition in RV144. Methods: Of the women enrolled in RV144, 777 vaccine and 807 placebo recipients were eligible and randomly selected according to their pre-vaccination HSV-1 and HSV-2 serostatus for analysis. Immunoglobulin G (IgG) and IgA responses to gD were determined by a binding antibody multiplex assay and HSV-2 serostatus was determined by Western blot analysis. Ninety-three percent and 75% of the vaccine recipients had anti-gD IgG and IgA responses two weeks post last vaccination, respectively. There was no evidence of reduction in HSV-2 infection by vaccination compared to placebo recipients over 78 weeks of follow-up. The annual incidence of HSV-2 infection in individuals who were HSV-2 negative at baseline or HSV-1 positive and HSV-2 indeterminate at baseline were 4.38/100 personyears (py) and 3.28/100 py in the vaccine and placebo groups, respectively. Baseline HSV- 1 status did not affect subsequent HSV-2 acquisition. Specifically, the estimated odds ratio of HSV-2 infection by Week 78 for female placebo recipients who were baseline HSV-1 positive (n = 422) vs. negative (n = 1120) was 1.14 [95% confidence interval 0.66 to 1.94, p = 0.64)]. No evidence of reduction in the incidence of HSV-2 infection by vaccination was detected. Conclusions: AIDSVAX® B/E containing gD did not confer protection from HSV-2 acquisition in HSV-2 seronegative women, despite eliciting anti-gD serum antibodies.en_US
dc.identifier.citationPLoS ONE. Vol.12, No.5 (2017)en_US
dc.identifier.doi10.1371/journal.pone.0176428en_US
dc.identifier.issn19326203en_US
dc.identifier.other2-s2.0-85019165739en_US
dc.identifier.urihttps://repository.li.mahidol.ac.th/handle/20.500.14594/41461
dc.rightsMahidol Universityen_US
dc.rights.holderSCOPUSen_US
dc.source.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85019165739&origin=inwarden_US
dc.subjectAgricultural and Biological Sciencesen_US
dc.subjectBiochemistry, Genetics and Molecular Biologyen_US
dc.titleAntibody to HSV gD peptide induced by vaccination does not protect against HSV-2 infection in HSV-2 seronegative womenen_US
dc.typeArticleen_US
dspace.entity.typePublication
mu.datasource.scopushttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=85019165739&origin=inwarden_US

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