grant

Chronic HIV infection and ischemic retinopathies

Organization AUGUSTA UNIVERSITYLocation AUGUSTA, UNITED STATESPosted 1 Feb 2025Deadline 31 Jan 2027
NIHUS FederalResearch GrantFY2025AIDS VirusAIDS drugsAccelerationAcquired Immune Deficiency Syndrome VirusAcquired Immunodeficiency Syndrome VirusAgeAge related macular degenerationAge-Related MaculopathyAnti-AIDS AgentsAnti-AIDS DrugsAnti-HIV AgentsAnti-HIV DrugsAnti-Human Immunodeficiency Virus AgentsAnti-Retroviral AgentsAnti-viral TherapyAssayBioassayBiochemicalBiological AssayBlindnessBlood VesselsCardiovascularCardiovascular Body SystemCardiovascular DiseasesCardiovascular Organ SystemCardiovascular systemCell AgingCell SenescenceCellular AgingCellular SenescenceChronicChronic DiseaseChronic IllnessCirculationClinicalClinical ResearchClinical StudyDataDevelopmentDiabetic RetinopathyDiseaseDisorderDrugsDysfunctionExperimental ModelsFunctional disorderGoalsHIVHIV InfectionsHTLV-III InfectionsHTLV-III-LAV InfectionsHeart VascularHuman Immunodeficiency VirusesHuman T-Lymphotropic Virus Type III InfectionsImmunocompromisedImmunocompromised HostImmunocompromised PatientImmunohistochemistryImmunohistochemistry Cell/TissueImmunohistochemistry Staining MethodImmunosuppressed HostIndividualInflammationIschemiaIschemia-Reperfusion InjuryLAV-HTLV-IIILifeLife ExpectancyLong-Term EffectsLymphadenopathy-Associated VirusMedicationMetabolicMetabolic DiseasesMetabolic DisorderMiceMice MammalsMonitorMorbidityMorbidity - disease rateMorphologyMurineMusNeurovascular dysfunctionNucleosidesOpportunistic InfectionsOutcomeOxidative StressPathogenicityPathologicPathologyPatientsPersonsPharmaceutical PreparationsPhysiopathologyProcessProteinsReperfusion DamageReperfusion InjuryReplicative SenescenceRetinaRetinal Blood VesselsRetinal DiseasesRetinal DisorderRetinal VesselsReverse Transcriptase InhibitorsRiskRisk FactorsThesaurismosisToxic effectToxicitiesTranscriptaseUncertaintyUpregulationVascular DiseasesVascular DisorderViral reservoirViremiaVirusVirus reservoirVirus-HIVWorkaccelerated agingaccelerated biological ageaccelerated biological agingage accelerationage associatedage correlatedage dependentage dependent macular degenerationage induced macular degenerationage linkedage relatedage related macular diseaseage related macular dystrophyage specificagesanti-retroviralantiAIDS agentbeta-L-2',3'-dideoxy-5-fluoro-3'-thiacytidineblood vessel disordercardiovascular disordercardiovascular riskcardiovascular risk factorchronic disordercirculatory systemcombinatorialcongenicdevelopmentaldoubtdrug/agentemtricitabineexperimentexperimental researchexperimental studyexperimentshigh riskimmunoreactivityimmunosuppressed patientmetabolism disordermortalitymouse modelmurine modelneuro-vascularneuro-vascular damageneuro-vascular injuryneurovascularneurovascular abnormalityneurovascular damageneurovascular dysregulationneurovascular impairmentneurovascular injuryneurovascular pathologyneurovasculopathynovelnucleoside analogpathophysiologypreventpreventingreplicative agingresponseretina blood vessel structureretina diseaseretina disorderretinal vascular networkretinal vascular structureretinal vasculatureretinopathysenescencesenescentsenile macular diseasesexvascularvascular dysfunctionvasculopathyviraemiaviral infectious disease treatmentviral sepsisvirusemiavision lossvisual loss
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Full Description

PROJECT SUMMARY
The overall goal of this novel exploratory proposal is to investigate/assess the potential impact of chronic HIV

infection and /or anti-HIV drugs on the development and progression of ischemic retinopathies. Combinatorial-

antiviral therapies (cART) have increased the life-expectancy of people living with HIV (PLWH), however these

patients carry not-detectable levels of virus that generate chronic inflammation leading to accelerated aging and

neurovascular dysfunction. Consequently, while HIV-related pathologies in immunocompromised patients are in

sharp decline, there is a significant increase in metabolic and cardiovascular morbidity and mortality in PLWH.

On the other hand, the contribution of long-term effects of cART as potential risk factor for cardiovascular

complications in PLWH is also still unclear. Ischemic retinopathies, that comprise known leading causes of

blindness (e.g. diabetic retinopathy and age-related macular degeneration), are associated with neurovascular

dysfunction and accelerated cellular senescence, thus implying that individuals presenting risk factors for the

occurrence of these pathogenic mechanisms, such as PLWH, could be at increased risk of developing more

aggressive forms of these diseases. Our preliminary studies, conducted in an experimental model recapitulating

chronic HIV infection (Tg26) and in mice treated with the nucleoside inverse transcriptase emtricitabine (FTC),

show significant structural changes of the retinal vasculature accompanied by increased retinal inflammation and

senescence markers. Therefore, herein we propose studies to validate our hypothesis that chronic HIV infections

and/or cART treatment accelerate and complicate the occurrence and progression of ischemic retinopathies.

Our aims are: Aim 1 Determine the neurovascular effects of chronic HIV infection on retinal neurovascular

integrity and in response to ischemia/reperfusion injury. Aim 2 Determine the neurovascular effects of anti-HIV

drugs on retinal neurovascular integrity and in response to ischemia/reperfusion injury.

Grant Number: 1R21EY037078-01
NIH Institute/Center: NIH

Principal Investigator: MANUELA BARTOLI

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