The Role of Eosinophils in the Lung Allograft

嗜酸性粒细胞在同种异体肺移植物中的作用

• 批准号: 10550167
• 负责人: Elizabeth A Jacobsen
• 金额: $ 51.28万
• 依托单位: UNIVERSITY OF MARYLAND BALTIMORE
• 依托单位国家: 美国
• 财政年份: 2019
• 资助国家: 美国
• 起止时间: 2019-02-01 至 2025-01-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10550167
• 关键词: Allograft Tolerance; Allografting; Antigen-Presenting Cells; Arginine; Attenuated; Biology; CD8-Positive T-Lymphocytes; Cell Communication; Cell Differentiation process; Cell physiology; Cells; Data; Dendritic Cells; Down-Regulation; Engraftment; Eotaxin; Failure; Goals; Graft Rejection; Human; ITGAX gene; Image; Immune response; Immune system; Immunity; Immunologics; Immunology; Immunosuppression; Immunosuppressive Agents; In Vitro; Infiltration; Inflammatory; Interleukin 2 Receptor; Interleukin-2; Laboratories; Lung; Lung Transplantation; Macrophage; Maintenance; Measures; Mediating; Mediator; Metabolism; Modification; Mus; Myeloid Cells; NOS2A gene; Nitric Oxide; Organ; Organ Survival; Organ Transplantation; Pathway interactions; Patients; Pattern; Pharmaceutical Preparations; Physiology; Play; Population; Post-Translational Protein Processing; Pre-Clinical Model; Production; Professional Role; Proliferating; Reactive Oxygen Species; Receptor Signaling; Regulation; Role; Signal Transduction; Small inducible cytokine A24; Solid; Source; Starvation; Synapses; T cell differentiation; T cell response; T memory cell; T-Cell Depletion; T-Cell Proliferation; T-Lymphocyte; Testing; Time; Translating; Transplant Recipients; Transplantation; Work; cell type; chemokine; critical period; design; effector T cell; eosinophil; granulocyte; heme oxygenase-1; improved; inducible gene expression; insight; lung allograft; mouse model; novel; novel therapeutic intervention; post-transplant; prevent; recruit; response; tumor-immune system interactions

PROJECT SUMMARY/ ABSTRACT It has become accepted canonical dogma that granulocytes, such as eosinophils, play a deleterious and uniformly destructive role in lung allograft survival. In direct contrast to this notion our laboratory has made the surprising observation that eosinophils are essential for lung allograft tolerance. Specifically, we demonstrate that in the presence of co-stimulatory blockade immunosuppression the lung allograft is rapidly infiltrated by a high numbers of inducible nitric oxide synthase positive eosinophils. This eosinophil population plays a critical role in the downregulation of T cell responses and ameliorating graft rejection. Depletion of eosinophils prior to engraftment prevents co-stimulatory blockade-mediated lung allograft tolerance. These findings led to our central hypothesis that early recruitment of eosinophils into the lung leads to allograft immunosuppression through iNOS-dependent pathways. Towards this hypothesis we propose three Specific Aims to define the cellular mechanism used by eosinophils to induce graft acceptance. In Aim 1 we propose to define the physiology of iNOS production and mechanism/s of immunosuppression in the lung allograft through use of eosinophil-specific iNOS pathway deficient mice, characterization of NO/ROS modification of T cells, and regulation of iNOS by heme-oxygenase 1. In Aim 2 we will define the role of professional antigen presenting cells in eosinophil-mediated immunosuppression by measuring eosinophil-specific mediators of that suppress dendritic cell activity, bi-directional interactions of eosinophils and dendritic cells, and live imaging of synaptic formation between these cells with T cells. In Aim 3 we will define the migratory patterns that contribute to eosinophil-mediated tolerance. We will complete this through measuring the effect of co-stimulatory blockade on eosinophil chemokine eotaxin-2 as well as determine the critical time point of eosinophil recruitment to the lungs using inducible eosinophil depletion mice. Our data will provide novel insight into cellular immune responses contributing to lung allograft tolerance and may shed light on the design of novel therapeutic strategies that are not currently being explored.

项目总结/摘要 粒细胞，如嗜酸性粒细胞，在细胞内起着有害的， 在同种异体肺移植物存活中的一致破坏性作用。与这一概念形成鲜明对比的是，我们的实验室 令人惊讶的发现是嗜酸性粒细胞对于肺同种异体移植耐受是必需的。具体来说，我们证明 在存在共刺激阻断免疫抑制的情况下， 大量诱导型一氧化氮合酶阳性嗜酸性粒细胞。这个嗜酸性粒细胞群体在 在下调T细胞反应和改善移植排斥中的作用。嗜酸性粒细胞耗竭 移植可防止共刺激阻断介导的肺移植耐受。这些发现导致我们 嗜酸性粒细胞早期聚集到肺中导致同种异体移植免疫抑制的中心假说 通过iNOS依赖的途径。针对这一假设，我们提出了三个具体目标来定义 嗜酸性粒细胞诱导移植物接受的细胞机制。在目标1中，我们建议定义 肺移植中诱导型一氧化氮合酶产生的生理学和免疫抑制机制 嗜酸性粒细胞特异性iNOS途径缺陷小鼠，表征T细胞的NO/ROS修饰，和 血红素加氧酶1对iNOS的调节作用在目标2中，我们将定义专职抗原呈递的作用， 通过测量抑制的嗜酸性粒细胞特异性介质， 树突状细胞活性，嗜酸性粒细胞和树突状细胞的双向相互作用，以及突触 在这些细胞与T细胞之间形成。在目标3中，我们将定义有助于 嗜酸性粒细胞介导的耐受。我们将通过测量共刺激阻断的效果来完成这一点 对嗜酸性粒细胞趋化因子eotaxin-2的影响，并确定嗜酸性粒细胞募集到 肺使用诱导型嗜酸性粒细胞耗竭小鼠。我们的数据将为细胞免疫提供新的见解 反应有助于肺移植耐受，并可能揭示新的治疗设计， 目前尚未探索的战略。

项目成果

Primary tumors from mucosal barrier organs drive unique eosinophil infiltration patterns and clinical associations.

• DOI: 10.1080/2162402x.2020.1859732
• 发表时间: 2020-12-30
• 期刊: Oncoimmunology
• 影响因子: 7.2
• 作者: Grisaru-Tal S;Itan M;Grass DG;Torres-Roca J;Eschrich SA;Gordon Y;Dolitzky A;Hazut I;Avlas S;Jacobsen EA;Ziv-Baran T;Munitz A
• 通讯作者: Munitz A