Traceless, aptamer-based cell isolation for cell therapy applications
Traceless, aptamer-based cell isolation for cell therapy applications
批准号:
10633756
负责人:
Suzie H. Pun
金额:
$34.25万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2023
资助国家:
美国
项目状态:
未结题
起止时间:
2023-06-01 至 2027-05-31
关键词:
AdoptionAntibodiesAutologousBindingBiologicalBiomanufacturingCAR T cell therapyCD34 geneCD4 Positive T LymphocytesCD8-Positive T-LymphocytesCD8B1 geneCell SeparationCell SurvivalCell TherapyCellsCellular immunotherapyClinicClinicalClinical TreatmentClinical TrialsCollectionComplexDNADataDendritic CellsDevelopmentDiabetes MellitusDiseaseEngineeringEnsureEthicsGene Expression ProfilingGenerationsGoalsHarvestHeart DiseasesHematologic NeoplasmsHumanImmune TargetingImmunotherapyLogisticsMacrophageMagnetismMembrane ProteinsMethodsOutcomePharmaceutical PreparationsPhenotypePopulationProductionRecombinantsRegenerative MedicineReportingReproducibilityResearchSELL geneSamplingSourceSpeedSpinal cord injuryT memory cellT-LymphocyteT-Lymphocyte SubsetsTNFRSF6 geneTechnologyTherapeuticTimeTranslationsUrineaptamercell transformationchimeric antigen receptor T cellscostgene productglycosylationimprovedinnovationmanufacturemonocytenext generationnovelperipheral bloodproteoliposomesreceptorregenerativeresponsesmall moleculestem cell therapystem cellssuccesstechnology platform
中文摘要
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英文摘要
PROJECT SUMMARY
Cell therapies are living drugs that can access a multifaceted biological response and can
therefore potentially provide not only therapeutic but also regenerative outcomes. However, these
beneficial attributes of cell therapeutics are accompanied by significantly more complex, variable,
and costly production logistics. Major advances in biomanufacturing are required for cell therapies
to have broad and widespread use. In this application, we propose to develop aptamer-based
technologies for cell separation that will provide an impactful improvement over current
technology, resulting in superior product at a fraction of the cost. Our main objectives are to 1)
establish a novel SELEX method for membrane proteins and identify new aptamers for cell
isolation applications, 2) develop methods for traceless isolation of monocytes and generation of
macrophage and dendritic cell products for immunotherapy, 3) demonstrate multiplexed selection
and T cell subset selection for CAR T cell immunotherapy applications, and 4) enable efficient
collection and expansion of urine stem cells as a source for regenerative medicine therapies.
Successful completion of these aims will lead to a platform technology for scalable and more
affordable production of CAR T cell immunotherapy, monocyte-based cell therapies and stem cell
treatments.
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