grant

In vivo cell engineering for HIV cure.

Organization UNIVERSITY OF SOUTHERN CALIFORNIALocation Los Angeles, UNITED STATESPosted 5 Sept 2025Deadline 30 Jun 2030
NIHUS FederalResearch GrantFY2025AIDS VirusAcquired Immune Deficiency Syndrome VirusAcquired Immunodeficiency Syndrome VirusAntibody-drug conjugatesAntigenic DeterminantsAntigensAreaB blood cellsB cellB cellsB-Cell DevelopmentB-CellsB-LymphocytesB-cellB220Binding DeterminantsBlood Precursor CellBody TissuesBone MarrowBone Marrow Reticuloendothelial SystemBypassC-C CKR-5C-C CKR-5 GeneC-C Chemokine Receptor Type 5C-C Chemokine Receptor Type 5 GeneCAR T cellsCAR modified T cellsCAR-TCAR-TsCC Chemokine Receptor 5CC-CKR-5CC-CKR-5 GeneCC-CKR5CCCKR5CCCKR5 GeneCCR-5CCR-5 GeneCCR5CCR5 ProteinCCR5 ReceptorsCCR5 geneCD195 AntigenCD195 Antigen GeneCD45CHEMR13CHEMR13 GeneCKR-5CKR-5 GeneCKR5CKR5 GeneCKR5 ReceptorsCMKBR5CMKBR5 GeneCell BodyCell TherapyCellsChemokine (C-C Motif) Receptor 5Chemokine (C-C) Receptor 5Chemokine (C-C) Receptor 5 GeneClinical TrialsCollaborationsDNA TherapyDevelopmentEffector CellEngineered GeneEngineeringEpitopesEvaluationFormulationGP180Gene DeliveryGene ModifiedGene Therapy VectorsGene Transduction AgentGene Transduction VectorsGene Transfer ClinicalGenetic InterventionHIVHIV resistanceHIV resistantHIV-1 Fusion Co-ReceptorHIV-1 Fusion Co-Receptor GeneHematopoietic Progenitor CellsHematopoietic stem cellsHospitalsHuman Immunodeficiency VirusesIn SituInjectionsKnock-outKnockoutLAV-HTLV-IIILMICLY5LentivirinaeLentivirusLightningLymphadenopathy-Associated VirusOrganoidsPTPRCPTPRC genePersonsPopulationPropertyProvirus IntegrationReagentRegimenSHIVSafetySurfaceT cells for CART-CellsT-LymphocyteT200TechnologyTherapeutic StudiesTherapy ResearchTissuesToxic effectToxicitiesVirus-HIVbase editingbase editorblood cell progenitorblood progenitorblood stem cellblood-forming stem cellcell based interventioncell engineeringcell mediated interventioncell mediated therapiescell-based therapeuticcell-based therapycellular engineeringcellular therapeuticcellular therapychallenge in rhesus macaqueschemotherapychimeric antigen T cell receptorchimeric antigen receptor (CAR) T cellschimeric antigen receptor Tchimeric antigen receptor T cellschimeric antigen receptor fusion protein T-cellschimeric antigen receptor modified T cellsconditioningcostcryogeldevelopmentaldirected differentiationexperiencefully-deleted adenoviral vectorfully-deleted adenovirus vectorgene editing platformgene editing systemgene editing technologygene editing toolsgene modificationgene repair therapygene therapygene-based therapygene-editing toolkitgenetic therapygenetically modifiedgenomic therapygutless adenoviral vectorgutless adenovirus vectorgutted adenoviral vectorgutted adenovirus vectorhdAdhelper-dependent adenoviral vectorhelper-dependent adenovirus vectorhematopoietic progenitorhematopoietic stem progenitor cellhemopoietic progenitorhemopoietic stem cellimmunogenin vivoindustrial partnershipindustry partnerindustry partnershipinfected rhesus macaquesinfected rhesus monkeyinfection in rhesus macaquesinfection of rhesus macaquesinhibitorinnovateinnovationinnovativeknockout genelipid based nanoparticlelipid nanoparticlelow and middle-income countriesmemberneutralizing antibodynon-human primatenonhuman primatenovelparticleprogenitor cell poolprogenitor cell populationprogenitor poolprogenitor populationprogramsrecombinaserhesus challengerhesus macaque challengerhesus monkey infectionsimian HIVsimian human immunodeficiency virusstem and progenitor cell populationstem cell poolstem cell populationsupport toolsthymus derived lymphocytevector
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Description preview

ABSTRACT
Many innovative gene and cell therapy strategies are being considered for an HIV cure. However, for a cure to

be acceptable to people living with HIV (PLWH), it must not only be effective, but also have a favorable profile

of safety/toxicity, cost, practicality and accessibility. In this Program Project we are focused on developing an

HIV…

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