(PQ6) Mesenchymal stem cell based and immunocompetent mouse models of HIV/AIDS KSHV-driven sarcomagenesis

(PQ6) 基于间充质干细胞和免疫活性的 HIV/AIDS 小鼠模型 KSHV 驱动的肉瘤发生

• 批准号: 10388236
• 负责人: Sabita Roy
• 金额: $ 59.1万
• 依托单位: UNIVERSITY OF MIAMI SCHOOL OF MEDICINE
• 依托单位国家: 美国
• 财政年份: 2021
• 资助国家: 美国
• 起止时间: 2021-04-08 至 2026-03-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10388236
• 关键词: AIDS related cancer; AIDS/HIV problem; Acquired Immunodeficiency Syndrome; Address; Affect; Animal Model; Antibodies; Antibody Therapy; Automobile Driving; Biology; Bone Marrow; Cancer Etiology; Cell model; Cells; Collaborations; Development; Doxorubicin; Engraftment; Evaluation; Fibroblast Growth Factor; Genes; Growth; HIV; HIV Infections; HIV-1; Herpesviridae; Herpesviridae Infections; Human; Human Herpesvirus 8; Human immunodeficiency virus test; IGF2 gene; Immune; Immune checkpoint inhibitor; Immunocompetent; Immunologic Deficiency Syndromes; Immunologic Tests; Immunologics; Immunosuppression; Immunotherapeutic agent; Immunotherapy; In Vitro; Inbred BALB C Mice; Incidence; Individual; Infection; Inflammatory; Kaposi Sarcoma; Local Therapy; Mesenchymal Stem Cells; Modeling; Molecular Genetics; Morbidity - disease rate; Mus; Mutation; Nude Mice; Oncogenes; Oncogenic; PD-1/PD-L1; PDGFRA gene; Pathogenesis; Patients; Phenotype; Phosphotransferases; Populations at Risk; Pre-Clinical Model; Preclinical Testing; Principal Investigator; Proteins; Role; Study models; System; T-Lymphocyte; Testing; Therapeutic; Translational Research; Transplantation; Tumorigenicity; Viral; Virus; Virus Diseases; antiretroviral therapy; base; chemotherapy; co-infection; common treatment; cytokine; design; epigenome; exhaustion; global health; immunoregulation; immunosenescence; immunosuppressed; imprint; in vivo; in vivo Model; innovation; lymph nodes; macrophage; mortality; mouse model; mutant; neoplastic cell; novel; novel therapeutic intervention; novel therapeutics; pre-clinical; pre-clinical research; programmed cell death ligand 1; programs; stem cell model; targeted treatment; transcriptome; tumor; tumor growth; tumorigenesis; tumorigenic

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.

卡波西肉瘤是一种与HIV/ AIDS相关的恶性肿瘤