Evaluation of a CCR5 Vaccine for HIV infection in the SIV/Macaque Model
Evaluation of a CCR5 Vaccine for HIV infection in the SIV/Macaque Model
批准号:
7943981
负责人:
Bryce C Chackerian
金额:
$50.0万
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:
2009-09-30 至 2012-08-31
关键词:
AddressAdverse effectsAntibodiesAntigenic VariationAntigensAutoantibodiesAutoantigensB-LymphocytesBindingCCR5 geneCD4 Lymphocyte CountChemokine (C-C Motif) Receptor 5Combined VaccinesDataDevelopmentEffectivenessEpitopesEvaluationFailureGeneticGrantHIVHIV InfectionsHIV ReceptorsHIV vaccineHumoral ImmunitiesImmuneImmune responseImmunizationImmunoglobulin GIndividualInfectionIntramuscularMacacaMacaca mulattaMeasuresModelingMonitorMucosal Immune ResponsesPathogenesisPeptidesPhenotypePlayProteinsProtocols documentationPublishingRegimenRoleRouteSIVSurfaceTestingVaccinatedVaccinationVaccine Clinical TrialVaccinesVaginaViralViral Load resultVirusVirus-like particleWorkbasedensityexperiencehuman diseaseimmunogenicimmunogenicityinterestpreventprimary outcomeprophylacticpublic health relevanceresponsesecondary outcometransmission processvaccine development
中文摘要
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英文摘要
DESCRIPTION (provided by applicant): Evaluation of a CCR5 Vaccine for HIV Infection in the SIV/Macaque Model. HIV vaccine development has been complicated by the extensive antigenic variation displayed by HIV. As an alternative to targeting the virus, we have developed vaccines targeting CCR5, a self- protein that is critically involved in HIV replication, transmission, and pathogenesis. By displaying peptides derived from CCR5 at high density on the surface of virus-like particles (VLPs), we have shown that we can efficiently overcome the mechanisms of B cell tolerance that normally limit the ability to induce high-titer IgG antibodies against self-proteins. Our VLP-based vaccines induce high- titer IgG antibodies against CCR5, these antibodies bind to native CCR5 and inhibit viral replication. In this project, we will evaluate the ability of a VLP-based vaccine targeting CCR5 to inhibit mucosal SIV infection of macaques. In Aim 1 we will evaluate the immunogenicity of our vaccines upon intramuscular and intravaginal inoculation. In Aim 2 we will challenge rhesus macaques via a vaginal challenge protocol and assess the protection provided by vaccination. These studies will allow us to assess the potential of vaccines targeting CCR5 to protect against HIV infection.
PUBLIC HEALTH RELEVANCE: In this project, we will evaluate the ability of a VLP-based vaccine targeting the HIV receptor, CCR5, to prevent SIV infection in macaques.
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海外基金