Virocide as an Anti-HIV Microbicide Candidate
Virocide as an Anti-HIV Microbicide Candidate
批准号:
7850370
负责人:
PHILIPPE ANDRE GALLAY
金额:
$45.14万
依托单位国家:
美国
项目类别:
财政年份:
2009
资助国家:
美国
项目状态:
已结题
起止时间:
2009-07-22 至 2011-06-30
关键词:
Amino AcidsAntiviral AgentsBindingBiological AssayCell ProliferationCell membraneCellsCellular MembraneCoitusDendritic CellsDevelopmentDoseDrug resistanceEnvironmentEpithelialEpitheliumExhibitsFemaleFigs - dietaryGenerationsGenital systemGenomicsGlycoproteinsGoalsHIVHIV Entry InhibitorsHIV InfectionsHIV-1HIV-2Hepatitis C virusHerpes Simplex InfectionsHourHumanImmuneImmune responseIn VitroInfectionInflammationInflammatoryInterferonsIntravaginal AdministrationLengthLesionLifeLiquid substanceLocal MicrobicidesMacacaMediatingMembraneModelingMucous MembraneMusMutationN-terminalNonstructural ProteinNucleosidesOryctolagus cuniculusPan GenusPathway interactionsPeptide HydrolasesPeptide antibodiesPeptidesPlayPositioning AttributePropertyProtease InhibitorRNA-Directed DNA PolymeraseReportingResearch DesignResistanceResistance developmentRoleSafetySatellite VirusesSeminal PlasmaSexual TransmissionSignal PathwaySimplexvirusSpecificityStomatitisSurfaceT-LymphocyteTestingTimeToll-like receptorsToxic effectVaginaVaginal DouchingVesicular stomatitis Indiana virusViralViral ProteinsVirusWorkanti-HIV microbicidecell typechemokinecytokinecytotoxicityimmunogenicimmunogenicityimprovedin vitro testingin vivoinhibitor/antagonistmalemicrobicidemouse modelnovelparticlepre-clinicalpressurepreventpublic health relevanceresearch studyresponsesedimentation velocitysimian human immunodeficiency virustransmission processvaginal transmission
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Topical microbicides are defined as vaginally applied products that prevent male-to-female or female-to-male HIV transmission. The high error rate of the HIV reverse transcriptase (RT) drives the development of resistance and genomic diversity in HIV. The current pan-resistance to all classes of HIV inhibitors, such as those found in O group virus for non-nucleoside RT and protease (PR) inhibitors, raises an important question with regard to the development of microbicides targeting RT or PR. These concerns may be extended to inhibitors of HIV entry due to rapid emergence of mutations in the envelope (Env) glycoprotein under selective pressure. There is thus an urgent need to identify new anti-HIV compounds, which target viral components other than PR, RT and Env, and which may be developed as safe and effective microbicides. We identified a short linear peptide called Virocide, which neutralizes HIV at an nM range. Several lines of evidence s cells even when applied twice daily to cells at a concentration 20-200-fold superior to that which blocks HIV infection; iii) Virocide does not harm mice injected i.v. twice daily with high peptide concentrations (0.5 mg) for a period of 3 days; and iv) Virocide apparently does not create lesions in the vaginal epithelium of humanized mice since the peptide, rather than promoting transmission, completely blocks intravaginal transmission. Virocide represents an attractive microbicide candidate for several reasons: i) Virocide inhibits infection of a broad range of primary isolates in various primary human cell types; ii) it interferes with the three mechanisms involved in HIV transmission: genital epithelial transmigration, dendritic cell-mediated transmission, and infection of mucosal target cells; iii) Virocide is extremely efficacious since less than 15 min of exposure suffices to neutralize HIV; iv) it is potent for two hours both prior to and after addition of HIV to cells, suggze the anti-HIV efficacy of Virocide in vitro as well as its toxicity and immunogenicity in vivo. If these studies unambiguously demonstrate that Virocide represents an attractive anti-HIV microbicide candidate, we will be in a position to test its efficacy as a topical microbicide in vivo.
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会议论文
Non-immunosuppressive Sanglifehrin Analogs as Therapeutic Agents for Viral Hepatitis-induced Liver Damage Development
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批准号:10594993
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项目类别:
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资助金额:$44.38万
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财政年份:2020
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负责人:PHILIPPE ANDRE GALLAY
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依托单位:
Non-immunosuppressive Sanglifehrin Analogs as Therapeutic Agents for Viral Hepatitis-induced Liver Damage Development
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批准号:9885794
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项目类别:
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资助金额:$44.38万
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财政年份:2020
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负责人:PHILIPPE ANDRE GALLAY
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依托单位:
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资助金额:$44.38万
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财政年份:2014
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依托单位:
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批准号:8207880
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项目类别:
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资助金额:$47.0万
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财政年份:2010
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依托单位:
C5a as an Anti-HIV Microbicidal Candidate
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批准号:8277245
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项目类别:
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财政年份:2010
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负责人:PHILIPPE ANDRE GALLAY
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依托单位:
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批准号:8073648
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项目类别:
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资助金额:$47.0万
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负责人:PHILIPPE ANDRE GALLAY
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依托单位:
Cyclophilins, Cyclophilin Inhibitors and Hepatitis C
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批准号:8011692
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项目类别:
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资助金额:$47.0万
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财政年份:2010
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资助金额:$47.48万
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财政年份:2010
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负责人:PHILIPPE ANDRE GALLAY
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Cyclophilins, Cyclophilin Inhibitors and Hepatitis C
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批准号:8602812
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项目类别:
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资助金额:$47.0万
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财政年份:2010
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负责人:PHILIPPE ANDRE GALLAY
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依托单位:
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批准号:8660266
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项目类别:
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资助金额:$47.0万
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财政年份:2010
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负责人:PHILIPPE ANDRE GALLAY
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依托单位:
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项目类别:
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资助金额:$28.49万
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财政年份:2009
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依托单位:
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财政年份:2009
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依托单位:
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项目类别:
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资助金额:$48.59万
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依托单位:
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负责人:PHILIPPE ANDRE GALLAY
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依托单位:
海外基金