Prevention of HIV-1 transmission by small-molecule CD4-mimetic entry inhibitors
Prevention of HIV-1 transmission by small-molecule CD4-mimetic entry inhibitors
批准号:
9411467
负责人:
NAVID MADANI
金额:
$63.79万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2017
资助国家:
美国
项目状态:
已结题
起止时间:
2017-07-14 至 2022-06-30
关键词:
AIDS preventionAcquired Immunodeficiency SyndromeAdverse effectsAnti-Retroviral AgentsAntibodiesAntibody ResponseAntiviral AgentsBindingBinding SitesCCR5 geneCD4 AntigensCXCR4 geneCellsDoseDrug TargetingEnvironmentEpidemicEtiologyEventFormulationGlycoproteinsGoalsHIVHIV Envelope Protein gp120HIV-1HIV-1 vaccineImmunologic Deficiency SyndromesIncidenceIncomeInfectionInterruptionInvestigationLaboratoriesLeadLife Cycle StagesMeasuresMediatingModalityModelingMolecular ConformationMonkeysMucous MembraneNatural Killer CellsProcessProphylactic treatmentProvirusesResearchSexual TransmissionStructureSurfaceTestingTimeVaccinesVaginaVaginal RingVaginal delivery procedureViralViral Reverse TranscriptionVirionVirusVirus DiseasesVirus InactivationWomanWorkabsorptionaqueousbasecell killingdesignimprovedinhibitor/antagonistmimeticsneutralizing antibodynonhuman primatenovelpandemic diseasepre-exposure prophylaxisprematurepreventprophylacticprotective efficacyreceptorresearch clinical testingsimian human immunodeficiency virussmall moleculetransmission processvaccine candidate
中文摘要
项目总结
英文摘要
PROJECT SUMMARY
Altering the course of the global AIDS epidemic will likely require the implementation of means to prevent the
transmission of human immunodeficiency virus (HIV-1). With no practical HIV-1 vaccine on the horizon,
modalities that would allow women to protect themselves from sexually acquired HIV-1 infection could exert an
immediate and significant impact on global HIV-1 incidence. An attractive prophylactic approach involves the
interruption of virus entry into the host cell, the earliest event in the HIV-1 life cycle. Small-molecule CD4-
mimetic compounds (smCMCs) bind within a conserved pocket on the HIV-1 envelope glycoprotein (Env) spike
and block the entry of the virus into the cell. In addition to interfering with the binding of HIV-1 to the CD4
receptor on the target cell, smCMCs also induce conformational changes in Env, irreversibly inactivating its
function. The binding of smCMCs also renders Env susceptible to inhibition by antibodies that can be elicited
by currently available HIV-1 Env vaccine candidates. Thus, in addition to their direct antiviral effect, smCMCs
can potentially synergize with vaccine-elicited antibodies to neutralize incoming HIV-1.
In this proposal, we will formulate a newly developed smCMC for sustained vaginal delivery via a pod-
intravaginal ring. The design parameters of the pod-intravaginal ring will be modified to optimize the release of
the smCMC. We will evaluate the vaginal delivery of the smCMC, as well as systemic absorption and potential
side effects, in monkeys. We will then examine the ability of the optimized pod-intravaginal ring delivering a
smCMC, alone or in combination with an Env-elicited antibody response, to protect monkeys from multiple low-
dose intravaginal challenges with a simian-human immunodeficiency virus (SHIV).
Establishing the ability of the pod-intravaginal ring to deliver protective concentrations of the smCMC to the
vaginal mucosa of monkeys in a sustained manner will set the stage for clinical testing of this prophylactic
approach in women.
期刊论文(0)
专著(0)
科研奖励(0)
会议论文
Design of dendrimeric HIV-1 transmission inhibitors targeting gp120 Phe-43 cavity
-
批准号:8135080
-
项目类别:
-
资助金额:$57.6万
-
财政年份:2010
-
负责人:NAVID MADANI
-
依托单位:
Biophysical characterization of chemokine receptors
-
批准号:6529765
-
项目类别:
-
资助金额:$4.62万
-
财政年份:2002
-
负责人:NAVID MADANI
-
依托单位:
Biophysical characterization of chemokine receptors
-
批准号:6463780
-
项目类别:
-
资助金额:$4.02万
-
财政年份:2001
-
负责人:NAVID MADANI
-
依托单位:
海外基金