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Autologous Humanized Mouse Model of Non-Small Cell Lung Cancer (NSCLC) to Investigate the Tumor-Immune Landscape and Its Response to Treatment

Autologous Humanized Mouse Model of Non-Small Cell Lung Cancer (NSCLC) to Investigate the Tumor-Immune Landscape and Its Response to Treatment
非小细胞肺癌 (NSCLC) 自体人源化小鼠模型,用于研究肿瘤免疫景观及其对治疗的反应
批准号:
10683397
负责人:
Michael Chiorazzi
金额:
$14.82万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2019
资助国家:
美国
项目状态:
已结题
起止时间:
2019-09-17 至 2024-08-31
关键词:
Active ImmunotherapyAddressAllogenicAnimal ModelAntibody TherapyAutologousB-LymphocytesBiological ProductsBiopsyBloodBone Marrow AspirationCancer EtiologyCancer PatientCellsClinical TrialsComplexDataDevelopmentDoctor of PhilosophyDrug usageEngraftmentExhibitsFailureFlow CytometryFunctional disorderGene Expression ProfileGeneticGenetic TranscriptionGenomic approachGenomicsGoalsGrowthGrowth FactorHarvestHematopoieticHematopoietic NeoplasmsHematopoietic SystemHematopoietic stem cellsHumanImmuneImmune System DiseasesImmune systemImmunofluorescence ImmunologicImmunooncologyImmunosuppressionImmunotherapeutic agentImmunotherapyIndividualInnate Immune SystemInstitutional Review BoardsInterventionKnowledgeLocationMacrophageManuscriptsMedical OncologyMentorshipMethodsMinorityModelingMusMyelogenousMyeloid CellsNatural Killer CellsNon-Small-Cell Lung CarcinomaOperative Surgical ProceduresPathway interactionsPatientsPharmaceutical PreparationsPhenotypePhysiciansPhysiologicalPopulationPostdoctoral FellowPre-Clinical ModelPreparationPrincipal InvestigatorProteomicsProtocols documentationResearchResearch PersonnelRoleSamplingScientistSystemT-LymphocyteTimeTissuesTrainingTreatment FailureTumor PromotionTumor-associated macrophagesTumor-infiltrating immune cellsVascular Endothelial Growth Factorsanti-PD-L1bevacizumabcareerclinical trainingdrug actiondrug efficacyexhaustexhaustiongenomic datahematopoietic engraftmenthumanized mouseimmune cell infiltrateimprovedimproved outcomeindividual patientmelanomamortalitymouse developmentmouse modelneoplastic cellpatient derived xenograft modelpatient responsepembrolizumabperipheral bloodreceptorresponsetreatment responsetumortumor growthtumor microenvironmenttumor-immune system interactions

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中文摘要
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英文摘要
PROJECT SUMMARY Non-small cell lung cancer (NSCLC) remains the major cause of cancer mortality across the globe, despite exciting advances in immune-based therapies. These therapies, while dramatically effective in some patients, are ineffective in the majority of NSCLC patients. The causes of treatment failure remain incompletely understood, as is the role of the local tumor microenvironment (TME) in influencing tumor growth, both in the presence and absence of these therapies. To better study human tumor-immune interactions and immunotherapeutics, we have developed a humanized mouse model that supports the engraftment of mice bearing a matched human hematopoietic system and tumor from an individual NSCLC patient. In addition, this model is unique in its support of functional myeloid cells as part of the innate immune system. We propose to use these autologously-engrafted humanized NSCLC PDX models to study the TME in detail, employing flow cytometric, immunostaining and single cell genomic analyses to characterize the transcriptional and proteomic states of the cells present. We will correlate tumor growth to specific cell populations identified with these methods, enhancing our understanding of the pathways active in tumor- vs blood-resident immune cells, and identifying established and possibly new networks of immune dysfunction in the TME. Armed with this knowledge, we will probe the pathways active in these patient models using drugs specific to the immune exhaustion and tumor promoting mechanisms we identify. Our goal is to gain a deeper understanding of how the TME and immunotherapeutics interact, and to develop these immune avatar mice as models that may predict a patient’s response to a particular immunotherapy. The principal investigator is a physician-scientist, with a PhD in genetics and post-doctoral and clinical training in Medical Oncology. His career goal is to become an independent investigator studying tumor-immune interactions. The proposed K08 training plan will provide the candidate with mentorship and coursework to build the expertise necessary to execute the proposed project and become independent in the field of translational immuno-oncology.
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Autologous Humanized Mouse Model of Non-Small Cell Lung Cancer (NSCLC) to Investigate the Tumor-Immune Landscape and Its Response to Treatment
  • 批准号:
    10019482
  • 项目类别:
  • 资助金额:
    $14.82万
  • 财政年份:
    2019
  • 负责人:
    Michael Chiorazzi
  • 依托单位:
Autologous Humanized Mouse Model of Non-Small Cell Lung Cancer (NSCLC) to Investigate the Tumor-Immune Landscape and Its Response to Treatment
  • 批准号:
    10472627
  • 项目类别:
  • 资助金额:
    $14.82万
  • 财政年份:
    2019
  • 负责人:
    Michael Chiorazzi
  • 依托单位:
Autologous Humanized Mouse Model of Non-Small Cell Lung Cancer (NSCLC) to Investigate the Tumor-Immune Landscape and Its Response to Treatment
  • 批准号:
    10248454
  • 项目类别:
  • 资助金额:
    $14.82万
  • 财政年份:
    2019
  • 负责人:
    Michael Chiorazzi
  • 依托单位:
Role of dre-1/FBXO11 in apoptosis
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