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Magnitude and Breadth of a Nonprotective Neutralizing Antibody Response in an Efficacy Trial of a Candidate HIV-1 gp120 Vaccine

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dc.contributor.author Montefiori, David en_US
dc.date.accessioned 2011-06-21T17:27:22Z
dc.date.available 2011-06-21T17:27:22Z
dc.date.issued 2010 en_US
dc.identifier.citation Gilbert,Peter;Wang,Maggie;Wrin,Terri;Petropoulos,Chris;Gurwith,Marc;Sinangil,Faruk;D'Souza,Patricia;Rodriguez-Chavez,Isaac R.;DeCamp,Allan;Giganti,Mike;Berman,Phillip W.;Self,Steve G.;Montefiori,David C.. 2010. Magnitude and Breadth of a Nonprotective Neutralizing Antibody Response in an Efficacy Trial of a Candidate HIV-1 gp120 Vaccine. Journal of Infectious Diseases 202(4): 595-605. en_US
dc.identifier.issn 0022-1899 en_US
dc.identifier.uri http://hdl.handle.net/10161/4155
dc.description.abstract Background. A candidate vaccine consisting of human immunodeficiency virus type 1 (HIV-1) subunit gp120 protein was found previously to be nonprotective in an efficacy trial (Vax004) despite strong antibody responses against the vaccine antigens. Here we assessed the magnitude and breadth of neutralizing antibody responses in Vax004. Methods. Neutralizing antibodies were measured against highly sensitive (tier 1) and moderately sensitive (tier 2) strains of HIV-1 subtype B in 2 independent assays. Vaccine recipients were stratified by sex, race, and high versus low behavioral risk of HIV-1 acquisition. Results. Most vaccine recipients mounted potent neutralizing antibody responses against HIV-1(MN) and other tier 1 viruses. Occasional weak neutralizing activity was detected against tier 2 viruses. The response against tier 1 and tier 2 viruses was significantly stronger in women than in men. Race and behavioral risk of HIV-1 acquisition had no significant effect on the response. Prior vaccination had little effect on the neutralizing antibody response that arose after infection. Conclusions. Weak overall neutralizing antibody responses against tier 2 viruses is consistent with a lack of protection in this trial. The magnitude and breadth of neutralization reported here should be useful for identifying improved vaccines. en_US
dc.language.iso en_US en_US
dc.publisher UNIV CHICAGO PRESS en_US
dc.relation.isversionof doi:10.1086/654816 en_US
dc.subject immunodeficiency-virus type-1 en_US
dc.subject recombinant glycoprotein-120 vaccine en_US
dc.subject aids vaccine en_US
dc.subject env clones en_US
dc.subject monoclonal-antibodies en_US
dc.subject infection en_US
dc.subject thailand en_US
dc.subject phase-3 en_US
dc.subject binding en_US
dc.subject panel en_US
dc.subject immunology en_US
dc.subject infectious diseases en_US
dc.subject microbiology en_US
dc.title Magnitude and Breadth of a Nonprotective Neutralizing Antibody Response in an Efficacy Trial of a Candidate HIV-1 gp120 Vaccine en_US
dc.title.alternative en_US
dc.description.version Version of Record en_US
duke.date.pubdate 2010-8-15 en_US
duke.description.endpage 605 en_US
duke.description.issue 4 en_US
duke.description.startpage 595 en_US
duke.description.volume 202 en_US
dc.relation.journal Journal of Infectious Diseases en_US

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