ROLE OF NON-NEUTRALIZING ANTIBODIES IN PROTECTION FROM HIV
ROLE OF NON-NEUTRALIZING ANTIBODIES IN PROTECTION FROM HIV
批准号:
8358104
负责人:
Ronald S. Veazey
金额:
$5.78万
依托单位国家:
美国
项目类别:
财政年份:
2011
资助国家:
美国
项目状态:
已结题
起止时间:
2011-05-01 至 2012-04-30
关键词:
AnimalsBindingBinding SitesControl AnimalDoseEpitopesFundingGrantHIVHIV Envelope Protein gp120HIV-1ImmunityIn VitroInfectionMacacaMeasuresMethodsMonoclonal AntibodiesNational Center for Research ResourcesPrimatesPrincipal InvestigatorPropertyResearchResearch InfrastructureResourcesRoleSexual TransmissionSourceUnited States National Institutes of HealthVaccine DesignVaccine ResearchVaccinesVirusVirus Activationcosthuman monoclonal antibodiesneutralizing antibodypreventresearch studyvaginal transmission
中文摘要
点击翻译按钮获取中文摘要
英文摘要
This subproject is one of many research subprojects utilizing the resources
provided by a Center grant funded by NIH/NCRR. Primary support for the subproject
and the subproject's principal investigator may have been provided by other sources,
including other NIH sources. The Total Cost listed for the subproject likely
represents the estimated amount of Center infrastructure utilized by the subproject,
not direct funding provided by the NCRR grant to the subproject or subproject staff.
In the absence of an effective vaccine, other methods for preventing the sexual transmission of human immunodeficiency virus type 1 (HIV-1) must be pursued. To guide vaccine design, we assessed whether human monoclonal antibodies (MAbs) b12 and b6 against the CD4 binding site on HIV-1 gp120 and F240 against an immundominant epitope on gp41 could prevent vaginal transmission of SHIVSF162P4 to macaques. The two anti-gp120 MAbs have similar monomeric gp120-binding properties, measured in vitro, but b12 is strongly neutralizing while b6 is not. F240 is non-neutralizing. Applied vaginally at a high dose, the strongly neutralizing MAb b12 provided sterilizing immunity in 7/7 animals, b6 in 0/5 animals and F240 in 2/5 animals. Compared to control animals, the protection by b12 achieved statistical significance whereas that due to F240 did not. Additional passive transfer experiments also indicated that the ability of the administered anti-gp120 MAbs to neutralize the challenge virus was a critical influence on protection. Furthermore, there was a significant increase in the number of founder viruses establishing infection in animals receiving MAb b6, compared to other non-protected macaques. Thus a gp120-binding, non-neutralizing MAb against gp120 was, at best, completely ineffective at protection. Non-neutralizing antibodies to gp41 may have a limited capacity to protect, but the results suggest that the central focus of HIV-1 vaccine research should be on the induction of virus-neutralizing antibodies.
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依托单位:
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项目类别:
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资助金额:$5.72万
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负责人:Ronald S. Veazey
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依托单位:
IMPORTANCE OF ANTIBODY ISOTYPE IN VAGINAL HIV TRANSMISSION
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批准号:8358084
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项目类别:
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资助金额:$5.78万
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负责人:Ronald S. Veazey
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依托单位:
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批准号:8358102
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项目类别:
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资助金额:$5.78万
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依托单位:
INTERSUBTYPE RECOMBINANTS FOR POLYVALENT ANTI-HIV VACCINE
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资助金额:$5.78万
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依托单位:
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项目类别:
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资助金额:$5.78万
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批准号:8358080
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项目类别:
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资助金额:$5.78万
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负责人:Ronald S. Veazey
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依托单位:
EARLY EVENTS IN MUCOSAL SIV PATHOGENESIS
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批准号:8358121
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项目类别:
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资助金额:$5.78万
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财政年份:2011
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负责人:Ronald S. Veazey
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依托单位:
THE EFFECTS OF ALCOHOL ON SIV PATHOGENESIS
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项目类别:
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资助金额:$5.78万
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负责人:Ronald S. Veazey
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批准号:8358103
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项目类别:
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资助金额:$5.78万
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负责人:Ronald S. Veazey
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批准号:8358024
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项目类别:
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资助金额:$5.78万
-
财政年份:2011
-
负责人:Ronald S. Veazey
-
依托单位:
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