(PQ6) Mesenchymal stem cell based and immunocompetent mouse models of HIV/AIDS KSHV-driven sarcomagenesis
(PQ6) Mesenchymal stem cell based and immunocompetent mouse models of HIV/AIDS KSHV-driven sarcomagenesis
批准号:
10388236
负责人:
Sabita Roy
金额:
$59.1万
依托单位国家:
美国
项目类别:
财政年份:
2021
资助国家:
美国
项目状态:
未结题
起止时间:
2021-04-08 至 2026-03-31
关键词:
AIDS related cancerAIDS/HIV problemAcquired Immunodeficiency SyndromeAddressAffectAnimal ModelAntibodiesAntibody TherapyAutomobile DrivingBiologyBone MarrowCancer EtiologyCell modelCellsCollaborationsDevelopmentDoxorubicinEngraftmentEvaluationFibroblast Growth FactorGenesGrowthHIVHIV InfectionsHIV-1HerpesviridaeHerpesviridae InfectionsHumanHuman Herpesvirus 8Human immunodeficiency virus testIGF2 geneImmuneImmune checkpoint inhibitorImmunocompetentImmunologic Deficiency SyndromesImmunologic TestsImmunologicsImmunosuppressionImmunotherapeutic agentImmunotherapyIn VitroInbred BALB C MiceIncidenceIndividualInfectionInflammatoryKaposi SarcomaLocal TherapyMesenchymal Stem CellsModelingMolecular GeneticsMorbidity - disease rateMusMutationNude MiceOncogenesOncogenicPD-1/PD-L1PDGFRA genePathogenesisPatientsPhenotypePhosphotransferasesPopulations at RiskPre-Clinical ModelPreclinical TestingPrincipal InvestigatorProteinsRoleStudy modelsSystemT-LymphocyteTestingTherapeuticTranslational ResearchTransplantationTumorigenicityViralVirusVirus Diseasesantiretroviral therapybasechemotherapyco-infectioncommon treatmentcytokinedesignepigenomeexhaustionglobal healthimmunoregulationimmunosenescenceimmunosuppressedimprintin vivoin vivo Modelinnovationlymph nodesmacrophagemortalitymouse modelmutantneoplastic cellnovelnovel therapeutic interventionnovel therapeuticspre-clinicalpre-clinical researchprogrammed cell death ligand 1programsstem cell modeltargeted treatmenttranscriptometumortumor growthtumorigenesistumorigenic
中文摘要
点击翻译按钮获取中文摘要
英文摘要
Kaposi’s sarcoma is an HIV/ AIDS associated malignancy that in spite of the implementation of
ART causes significant morbidity and mortality. Pathogenesis based design and testing of new
therapeutic approaches are hampered by the paucity of models that reproduce KSHV
oncogenesis in the HIV/AIDS setting. There are three major gaps to the experimental ability to
model AIDS-KS in vitro and in vivo for translational and preclinical research. 1) A continuous in
vitro KSHV-infection to tumorigenesis model that could help dissect microenvironment
contributions, and dissect viral and host contributions to viral oncogenesis 2) An in vitro and in
vivo model where HIV contributions to KSHV-sarcomagenesis can be identified and studied 3)
An immunocompetent model of KSHV-tumorigenesis that could be used to test immune-based
therapies. The Mesri and Roy Labs collaboratively developed a comprehensive set of cell and
animal models of KSHV-driven Kaposi’s sarcoma that include. I) A mesenchymal-stem cell KSHV-
infection to tumorigenesis system--a “de novo” KSHV-induced sarcomagenesis in vitro and in vivo
model, which is tightly dependent on the infected-cell microenvironment for tumorigenicity II) A
set of mouse models in which KSHV tumorigenesis occurs and can be studied in the context of
immunodeficiency, HIV-infection contributions to tumorigenesis and KSHV tumorspecific
immunosuppression III) A unique model in which KSHV-infected tumors can be transplanted and
grown in HIV infected Balb/c mice. In Aim (1) we will use the MSCs models study the role of KSHV
and HIV interactions in viral oncogenesis of HIV/AIDS-KS. In Aim (2) we will determine the
mechanisms whereby HIV infection promotes KSHV tumorigenicity in nude and
immunocompetent mice. In Aim (3), we will use our model of KSHV-tumorigenesis in HIV infected
immunocompetent mice as AIDS-KS preclinical model. We will be able to test immunological
therapies to KS such as immunomodulatory molecules, antibody-targeted therapies and
checkpoint inhibitor immunotherapies. The propose studies provide unique mouse models to
study the role of KSHV HIV co-infection in the pathogenesis of HIV/AIDS-associated Kaposi’s
sarcoma and will serve to pre-clinically evaluate novel AIDS-KS therapeutic treatments.
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(PQ6) Mesenchymal stem cell based and immunocompetent mouse models of HIV/AIDS KSHV-driven sarcomagenesis
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批准号:10609000
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项目类别:
-
资助金额:$59.93万
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财政年份:2021
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负责人:Sabita Roy
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依托单位:
Role of Gut Microbiome- Brain Axis in Modulating CNS Inflammasomes in the Neuropathology Produced by Opioid Exposure and HIV
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批准号:10434855
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项目类别:
-
资助金额:$37.87万
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财政年份:2019
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负责人:Sabita Roy
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依托单位:
Multidisciplinary Training in Substance Abuse Research
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批准号:10395444
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项目类别:
-
资助金额:$27.01万
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财政年份:2019
-
负责人:Sabita Roy
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依托单位:
Role of Gut Microbiome- Brain Axis in Modulating CNS Inflammasomes in the Neuropathology Produced by Opioid Exposure and HIV
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批准号:10434466
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项目类别:
-
资助金额:$8.46万
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财政年份:2019
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负责人:Sabita Roy
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依托单位:
Role of Gut Microbiome- Brain Axis in Modulating CNS Inflammasomes in the Neuropathology Produced by Opioid Exposure and HIV
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批准号:10518777
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项目类别:
-
资助金额:$4.43万
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财政年份:2019
-
负责人:Sabita Roy
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依托单位:
Role of Gut Microbiome- Brain Axis in Modulating CNS Inflammasomes in the Neuropathology Produced by Opioid Exposure and HIV
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批准号:10653501
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项目类别:
-
资助金额:$15.35万
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财政年份:2019
-
负责人:Sabita Roy
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依托单位:
Role of Gut Microbiome- Brain Axis in Modulating CNS Inflammasomes in the Neuropathology Produced by Opioid Exposure and HIV
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批准号:10754697
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项目类别:
-
资助金额:$4.43万
-
财政年份:2019
-
负责人:Sabita Roy
-
依托单位:
Role of Gut Microbiome- Brain Axis in Modulating CNS Inflammasomes in the Neuropathology Produced by Opioid Exposure and HIV
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批准号:10197088
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项目类别:
-
资助金额:$37.87万
-
财政年份:2019
-
负责人:Sabita Roy
-
依托单位:
Role of Gut Microbiome- Brain Axis in Modulating CNS Inflammasomes in the Neuropathology Produced by Opioid Exposure and HIV
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批准号:10020183
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项目类别:
-
资助金额:$37.97万
-
财政年份:2019
-
负责人:Sabita Roy
-
依托单位:
Multidisciplinary Training in Substance Abuse Research
-
批准号:9919533
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项目类别:
-
资助金额:$25.25万
-
财政年份:2019
-
负责人:Sabita Roy
-
依托单位:
Role of Gut Microbiome- Brain Axis in Modulating CNS Inflammasomes in the Neuropathology Produced by Opioid Exposure and HIV
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批准号:10653833
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项目类别:
-
资助金额:$37.87万
-
财政年份:2019
-
负责人:Sabita Roy
-
依托单位:
Role of Gut Microbiome- Brain Axis in Modulating CNS Inflammasomes in the Neuropathology Produced by Opioid Exposure and HIV
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批准号:10119599
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项目类别:
-
资助金额:$8.46万
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财政年份:2019
-
负责人:Sabita Roy
-
依托单位:
Multidisciplinary Training in Substance Abuse Research
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批准号:10611853
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项目类别:
-
资助金额:$12.85万
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财政年份:2019
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负责人:Sabita Roy
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依托单位:
Role of Microbial dysbiosis and altered metabolomics in the context of Opioid abuse and ART in HIV disease progression
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批准号:10087914
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项目类别:
-
资助金额:$50.41万
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财政年份:2017
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负责人:Sabita Roy
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依托单位:
Microbial Dysbiosis and TLR2 Activation Contribute to Immune Activation, Inflammation and HIV Persistence in the Context of Opioid Abuse Despite ART Therapy
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批准号:10153742
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项目类别:
-
资助金额:$49.96万
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财政年份:2017
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负责人:Sabita Roy
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依托单位:
Microbial Dysbiosis and TLR2 Activation Contribute to Immune Activation, Inflammation and HIV Persistence in the Context of Opioid Abuse Despite ART Therapy
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批准号:9389140
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项目类别:
-
资助金额:$53.73万
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财政年份:2017
-
负责人:Sabita Roy
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依托单位:
Role of Microbial dysbiosis and altered metabolomics in the context of Opioid abuse and ART in HIV disease progression
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批准号:9253611
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项目类别:
-
资助金额:$59.3万
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财政年份:2017
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负责人:Sabita Roy
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依托单位:
Mechanism underlying Morphine modulation of gut barrier function in the Context o
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批准号:8975702
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项目类别:
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资助金额:$15.55万
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财政年份:2013
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负责人:Sabita Roy
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依托单位:
Mechanism underlying Morphine modulation of gut barrier function in the Context o
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批准号:8470846
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项目类别:
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资助金额:$31.0万
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财政年份:2013
-
负责人:Sabita Roy
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依托单位:
Mechanism underlying Morphine modulation of gut barrier function in the Context o
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批准号:9189597
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项目类别:
-
资助金额:$34.54万
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财政年份:2013
-
负责人:Sabita Roy
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依托单位: