grant

MR-guided focused ultrasound to eradicate CNS viral reservoirs and promote neurogenesis in the HIV-infected brain

Organization UNIVERSITY OF MARYLAND BALTIMORELocation BALTIMORE, UNITED STATESPosted 1 Jun 2021Deadline 30 Apr 2027
NIHUS FederalResearch GrantFY2026AIDS VirusAIDS/HIVAcquired Immune Deficiency Syndrome VirusAcquired Immunodeficiency Syndrome VirusAnti-Retroviral AgentsAwardBenign Essential TremorBindingBlood - brain barrier anatomyBlood-Brain BarrierBrainBrain Nervous SystemCNS Nervous SystemCRISPR approachCRISPR based approachCRISPR methodCRISPR methodologyCRISPR techniqueCRISPR technologyCRISPR toolsCRISPR-CAS-9CRISPR-based methodCRISPR-based techniqueCRISPR-based technologyCRISPR-based toolCRISPR/CAS approachCRISPR/Cas methodCRISPR/Cas technologyCRISPR/Cas9CRISPR/Cas9 technologyCas nuclease technologyCentral Nervous SystemClinicalClinical TrialsClustered Regularly Interspaced Short Palindromic Repeats approachClustered Regularly Interspaced Short Palindromic Repeats methodClustered Regularly Interspaced Short Palindromic Repeats methodologyClustered Regularly Interspaced Short Palindromic Repeats techniqueClustered Regularly Interspaced Short Palindromic Repeats technologyDNADeoxyribonucleic AcidDevelopmentDrugsEmergent TechnologiesEmerging TechnologiesEncephalonEnsureEssential TremorFocused UltrasoundHIVHIV 1 associated neurocognitive disorderHIV associated neurocognitive deficitHIV associated neurocognitive impairmentHIV cureHIV functional cureHIV individualsHIV induced neurocognitive deficitHIV induced neurocognitive impairmentHIV infected individualsHIV infected personsHIV neurocognitive impairmentHIV peopleHIV positive individualsHIV positive peopleHIV-1 associated neurocognitive deficitHIV-1 associated neurocognitive disorderHIV-1 associated neurocognitive impairmentHIV-1 cureHIV-1 functional cureHIV-associated neurocognitive disorderHIV/AIDSHIV/AIDS cureHemato-Encephalic BarrierHortega cellHumanHuman Immunodeficiency VirusesLAV-HTLV-IIILymphadenopathy-Associated VirusMarylandMedicationMicrogliaModern ManMolecular InteractionNIDANational Institute of Drug AbuseNational Institute on Drug AbuseNervous System DiseasesNervous System DisorderNeuraxisNeurocognitive Impairment in HIVNeurocognitive Impairment in HIV-1Neurologic DisordersNeurological DisordersPLWHPWHParalysis AgitansParkinsonParkinson DiseasePatientsPatternPharmaceutical PreparationsPhysiologic pulsePreclinical dataPrimary ParkinsonismPulseResearchResearch ResourcesResourcesRodentRodent ModelRodentiaRodents MammalsSelf AdministeredSelf AdministrationSeveritiesSourceSubgroupSubstance Use DisorderTechniquesTranslatingTreatment ProtocolsTreatment RegimenTreatment ScheduleUniversitiesViral BurdenViral LoadViral Load resultViral reservoirVirusVirus reservoirVirus-HIVaddictionaddictive disorderanti-retroviralantiretroviral therapyantiretroviral treatmentbloodbrain barrierclinical translationclinically translatabledevelopmentaldrug/agentgitter cellhuman immunodeficiency virus cureimprovedindividuals infected with HIVindividuals with HIVindividuals with human immunodeficiency virusmesogliamicroglial cellmicrogliocyteneural controlneural regulationneurogenesisneurological diseaseneuromodulationneuromodulatoryneuroregulationpeople infected with HIVpeople infected with human immunodeficiency viruspeople living with HIVpeople with HIVpeople with human immunodeficiency virusperivascular glial cellpreclinical findingspreclinical informationpreventpreventingprogramssite targeted deliverysubstance use and disordersuccesstargeted delivery
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Full Description

Project Summary:
This DP1 application responds to PAR-20-221 “NIDA Avant-Garde Award Program for

HIV/AIDS and Substance Use Disorder Research”. The PI, Linda Chang, proposes to tackle a

major challenge in the treatment or cure for HIV, namely, the inability of current treatment

regimens to eradicate the viral reservoirs, especially those that are protected by the blood brain

barrier (BBB) in the central nervous system (CNS). HIV-infected persons who have substance

use disorders (SUDs) often have even higher viral loads and suffer from greater severity of HIV-

associated neurocognitive disorders (HAND). She proposes to use the emerging technology of

MR-guided focused ultrasound (MRgFUS) to safely and transiently open the BBB in order to

maximize the delivery of long-acting slow release antiretroviral therapy (LASER ART), and to

provide targeted delivery of CRISPR-Cas9 to eliminate the integrated HIV proviral DNA in the

CNS viral reservoirs. The combined approach of LASER ART, followed by AAV-CRISPR-Cas9

has shown early successes in subgroups of rodent models, but further optimal delivery of these

agents to the CNS is needed. First, HIV-humanized rodent models will be used to demonstrate

markedly improved delivery of these agents into the CNS, and the efficacy of eliminating the

virus without rebounds. Furthermore, since the same FUS energy and pulse patterns used for

BBB opening can also induce neurogenesis and activate microglia, these secondary effects will

be evaluated as well. Lastly, due to compelling early preclinical findings with neuromodulation

by others, low-intensity MRgFUS as a potential treatment for addiction will also be explored in

drug self-administration rodent models. The PI has assembled an outstanding team of

collaborators who are experts in each of the techniques and approaches required to ensure the

success of the proposed research. Furthermore, since MRgFUS, at higher intensities, is

currently being used in the clinical settings to successfully treat patients with essential tremors

or Parkinson’s disease, and at different parameters (e.g., pulsed high intensity, low intensity,

etc.) and hardware configurations in clinical trials of other neurological disorders, the proposed

research has a high potential for clinical translation. Given the available resources and expertise

at the University of Maryland, pilot clinical trials may start in years 3-5. In summary, the

proposed research to use MRgFUS to maximize the delivery of HIV elimination agents may

ultimately eradicate the HIV viral reservoirs, especially those in the CNS, and halt the

progression or prevent the development of HAND, particularly for those with SUDs.

Grant Number: 5DP1DA053719-05
NIH Institute/Center: NIH

Principal Investigator: LINDA CHANG

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