Investigating IL-10-producing suppressive NK cells

研究产生 IL-10 的抑制性 NK 细胞

• 批准号: 10189502
• 负责人: Kristina Stoermer Burrack
• 金额: $ 10.8万
• 依托单位: HENNEPIN HEALTHCARE RESEARCH INSTITUTE
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-06-12 至 2022-09-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/10189502
• 关键词: Address; Age; Antibodies; Autoimmunity; Basic Science; Biological; Biometry; CD8-Positive T-Lymphocytes; Cell physiology; Cells; Cerebral Malaria; Cerebrovascular system; Cerebrum; Cessation of life; Child; Clinic; Clinical; Communicable Diseases; Complex; Complication; Core Facility; Cytoprotection; Data; Development; Disease; Endothelial Cells; Flow Cytometry; Foundations; Goals; Health Care Research; Human; Immune; Immune response; Immunity; Immunologist; Immunology; Infection; Infectious Diseases Research; Institution; Interleukin-10; Interleukin-15; Knockout Mice; Knowledge; Malaria; Mediating; Mentors; Minnesota; Modeling; Molecular Analysis; Mouse Strains; Mus; NK Cell Activation; Natural Killer Cells; Neurologic Deficit; Outcome; Parasites; Pathogenesis; Pathologic; Pathology; Pharmacology; Phase; Plasmodium berghei; Population; Positioning Attribute; Production; Reporting; Research; Research Institute; Research Personnel; Resource Sharing; Role; STAT3 gene; Signal Pathway; Signal Transduction; T cell regulation; T cell response; T-Lymphocyte; Therapeutic; Universities; Work; animal facility; base; blood-brain barrier disruption; cancer immunotherapy; career; cell type; cellular targeting; cytokine; cytotoxic; design; global health; human disease; immunopathology; inhibitor/antagonist; interest; knockout gene; mouse model; novel; novel strategies; novel therapeutic intervention; pathogen; prevent; prophylactic; protective effect; receptor; response; tumor growth; vaccine immunotherapy

PROJECT SUMMARY/ABSTRACT Dr. Kristina Burrack’s research has led to the identification of a cytokine complex treatment that stimulates natural killer (NK) cells to produce the immunosuppressive cytokine IL-10 and prevents mice from dying from an immune-mediated disease following Plasmodium infection known as cerebral malaria. Malaria is a significant global health problem with more than 200 million clinical cases and nearly 500,000 deaths annually. Cerebral malaria (CM) is a deadly complication of Plasmodium infection that mostly afflicts children under the age of five and can result in long-term neurologic deficits in children who survive. In the human disease and the mouse model of cerebral malaria, a pathologic immune response is thought to contribute to disruption of the blood brain barrier. In the present proposal, Dr. Burrack will more fully elucidate the role of cytokine complex-stimulated NK cells in cerebral malaria and the induction of IL-10 in human and mouse NK cells. In addition to direct support from mentors and collaborators, Dr. Burrack has full access to the shared resources in the Center for Immunology at the University of Minnesota, including core facilities in flow cytometry, animal facilities, and biostatistics. Interactions with collaborators at the University of Minnesota, Hennepin Healthcare Research Institute, the Mayo Clinic, and elsewhere will allow her to gain further expertise in the analysis of molecular signaling pathways, analyze human NK cells, generate new mouse strains, and further investigate the cerebral malaria mouse model, which will be critical as she transitions into the independent phase of her career. The data generated from the proposed studies will form the basis for an R01 application. The proposed studies are significant because they address a critical gap in basic research that is needed to fully characterize NK cell activation following cytokine stimulation – specifically, how to induce IL-10-producing suppressive NK cells – and understand the mechanisms that prevent fatal immunopathology. These findings will have major clinical implications for the design of adjunctive therapies for human cerebral malaria and other immunopathologic diseases and inform the development of novel NK cell-directed therapies. Dr. Burrack’s long-term goal is to dedicate her career to advancing basic and translational immunology and infectious disease research as an independent investigator at an academic institution. As an immunologist with a deep interest and proven track record in studying the pathogenesis of infectious diseases of global health importance, she is in a unique position to answer the questions set forth in this proposal and to rapidly advance the understanding of how to tune NK cell stimulation to prevent immunopathology and the role of IL-10- producing NK cells in the pathogenesis of cerebral malaria.

项目摘要/摘要 克里斯蒂娜·伯拉克博士的研究导致了一种细胞因子复合体疗法的确定，这种疗法可以刺激 自然杀伤(NK)细胞产生免疫抑制细胞因子IL-10并防止小鼠死于 疟原虫感染后的一种免疫介导性疾病，称为脑型疟疾。疟疾是一种 这是一个严重的全球健康问题，每年有2亿多个临床病例和近50万人死亡。 脑型疟疾(CM)是疟原虫感染的一种致命并发症，主要困扰儿童。 5岁，并可能导致存活儿童的长期神经缺陷。在人类疾病和 脑型疟疾的小鼠模型，一种病理免疫反应被认为有助于破坏 血脑屏障。在目前的提案中，伯拉克博士将更全面地阐明细胞因子的作用 脑型疟疾中复杂刺激的NK细胞以及人和小鼠NK细胞中IL-10的诱导。在……里面 除了导师和合作者的直接支持外，伯拉克博士还可以完全访问共享资源 在明尼苏达大学免疫学中心，包括流式细胞术的核心设施，动物 设施和生物统计学。与明尼苏达大学Hennepin Healthcare的合作者互动 研究所，梅奥诊所和其他地方将使她获得进一步的专业知识，分析 分子信号通路，分析人类NK细胞，产生新的小鼠品系，并进一步研究 脑疟疾小鼠模型，这将是至关重要的，因为她过渡到她的独立阶段 职业生涯。拟议研究产生的数据将构成R01申请的基础。建议数 研究具有重要意义，因为它们解决了基础研究中的关键差距，这是充分描述特征所需的 细胞因子刺激后的NK细胞活化--特别是如何诱导产生IL-10的抑制性NK细胞 细胞--并了解防止致命免疫病理的机制。这些发现将对 人类脑型疟疾及其他疾病辅助疗法设计的临床意义 免疫病理疾病，并为新的NK细胞导向疗法的发展提供信息。伯拉克医生的 长期目标是将她的职业生涯献给促进基础和翻译免疫学和传染病 作为一家学术机构的独立研究员从事疾病研究。作为一名免疫学家，他有着深刻的 对研究全球卫生传染病的发病机制感兴趣并有良好的记录 重要的是，她处于独特的地位，可以回答这项提案中提出的问题，并迅速推进 了解如何调节NK细胞刺激以预防免疫病理以及IL-10的作用 脑型疟疾发病机制中NK细胞的产生