Therapeutic strategies to improve function of high risk liver grafts

改善高危肝移植功能的治疗策略

• 批准号: 10115607
• 负责人: Andrew Serghios Barbas
• 金额: $ 18.77万
• 依托单位: DUKE UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2020
• 资助国家: 美国
• 起止时间: 2020-02-28 至 2025-01-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10115607
• 关键词: Award; Binding; Biogenesis; Biological; Biology; Biometry; Cardiac Death; Cell Death; Cells; Cessation of life; Clinical; Clinical Trials; Data; Deacetylase; Development; Donor person; Elderly; Environment; Enzymes; Excision; Fatty Liver; Functional disorder; Gene Expression; Generations; Goals; Hepatocyte; Histologic; Human; In Vitro; Inflammation; Inflammatory; Injury; Intervention; Ischemia; Laboratories; Laboratory Research; Liver; Measures; Mediating; Mediator of activation protein; Membrane; Mentors; Mitochondria; Modeling; Molecular; Natural Immunity; Nutrient; Operative Surgical Procedures; Organ; Organ Donor; Organ Preservation; Outcome; Oxygen; Pathway interactions; Patients; Pattern; Perfusion; Physiological; Production; Program Development; Rattus; Reactive Oxygen Species; Receptor Activation; Recovery; Reperfusion Injury; Reperfusion Therapy; Research; Research Personnel; Resistance; SIRT1 gene; Scientist; Surgeon; Technology; Testing; Therapeutic; Toll-like receptors; Training; Translating; Transplantation; Transplantation Surgery; United States; Universities; Waiting Lists; Work; base; career; career development; clinical practice; clinically relevant; combat; cytokine; experience; experimental study; graft failure; graft function; high risk; improved; improved functioning; improved outcome; liver ischemia; liver transplantation; mitochondrial dysfunction; mortality; mouse model; novel; novel therapeutics; porcine model; post-transplant; pre-clinical; professor; public health relevance; skills; tool

PROJECT SUMMARY This proposal presents a five-year research career development program focused scientifically on improving the viability of liver grafts from extended criteria donors (ECD) for transplantation. The candidate is currently an Assistant Professor of Surgery at Duke University. The candidate has previous research and clinical experience in transplant surgery involving normothermic machine perfusion (NMP), whereby an organ is housed in an ex vivo environment and perfused with nutrients and oxygen under physiologic conditions. The candidate will now advance this technology by using NMP to deliver novel therapeutics to transplant grafts, and focus his research on mitochondrial contributions to graft dysfunction. The candidate has assembled a diverse mentoring committee of investigators with expertise in transplant surgery, NMP, molecular therapeutics, and mitochondrial biology. The proposed training and experiments will provide the candidate with a combined skillset in innate immunity, mitochondrial biology, transplant surgery, and biostatistics that will enable him transition to research independence as a surgeon-scientist dedicated to reducing the organ shortage in the field of transplant surgery. The primary obstacle facing the field of liver transplantation is the severe shortage of donor organs. In 2018, 8,000 liver transplants were performed in the United States, but another 13,000 patients remain on the waitlist. The mortality rate of patients on the waitlist is exceedingly high, at over 20% per year. One strategy with great potential to increase organ availability is utilization of extended criteria donors (ECDs). The ECD designation includes donors of advanced age (≥ 60 years), those with significant hepatic steatosis, and livers donated after cardiac death. However, widespread use of ECD livers has been limited by several factors, including increased rates of graft dysfunction, graft failure, and recipient death. These poor outcomes have been attributed to a reduced capacity of ECD livers to recover from ischemia-reperfusion (I-R) injury. I-R injury induces mitochondrial dysfunction in the graft that leads to cell death. The dying cells in the graft release a broad array of molecules known collectively as damage-associated molecular patterns (DAMPs), which are known to activate inflammatory and cell death pathways, leading to further graft injury. We hypothesize that reducing the damage caused by mitochondrial dysfunction and DAMPs will improve the viability of ECD livers for transplant and reduce the current shortage of livers available for transplantation. The use of NMP technology provides an ideal platform for delivering therapeutics to improve ECD graft function. This project will employ NMP technology to deliver therapeutics that enhance mitochondrial function and removing harmful DAMPs using our novel DAMP-capturing membrane. The aims of this proposal are: 1) determine the effects of enhanced mitochondrial function on ECD liver transplantation, 2) determine the effects of removing DAMPs on post-transplant graft injury and function.

项目摘要 该提案提出了一项为期五年的研究职业发展计划，重点是科学地提高 来自用于移植的扩展标准供体（ECD）的肝移植物的活力。候选人目前是一名 杜克大学外科助理教授。候选人有以前的研究和临床经验 在涉及常温机器灌注（NMP）移植手术中， 体内环境，并在生理条件下灌注营养素和氧气。候选人现在将 通过使用NMP为移植移植物提供新的治疗方法来推进这项技术，并专注于他的研究 线粒体对移植物功能障碍的影响候选人组建了一个多元化的指导委员会 在移植手术、NMP、分子治疗学和线粒体生物学方面具有专业知识的研究人员。 拟议的训练和实验将为候选人提供先天免疫方面的综合技能， 线粒体生物学，移植手术和生物统计学，这将使他过渡到研究 作为一名外科医生，科学家，致力于减少移植手术领域的器官短缺。 肝移植领域面临的主要障碍是供体器官的严重短缺。在2018年， 在美国进行了8,000例肝移植手术，但另有13,000名患者仍在等待名单上。 等候名单上的病人死亡率极高，每年超过20%。一个战略， 增加器官可用性的潜力是利用扩展标准供体（ECD）。ECD名称 包括高龄供体（≥ 60岁）、严重肝脂肪变性供体和 心源性死亡然而，ECD肝脏的广泛使用受到几个因素的限制，包括 移植物功能障碍、移植物衰竭和受体死亡率。这些不良结果归因于 ECD肝脏从缺血-再灌注（I-R）损伤中恢复的能力降低。I-R损伤诱导线粒体 导致细胞死亡的移植物功能障碍移植物中垂死的细胞释放出大量的分子 统称为损伤相关分子模式（DAMP），已知其激活 炎症和细胞死亡途径，导致进一步的移植物损伤。我们假设减少损伤 由线粒体功能障碍和DAMPs引起的急性排斥反应将提高ECD肝脏移植的存活率， 目前可供移植的肝脏短缺。NMP技术的使用提供了理想的平台 用于递送治疗剂以改善ECD移植物功能。该项目将采用NMP技术， 增强线粒体功能并使用我们的新型DAMP捕获技术去除有害DAMP的治疗方法 膜的本研究的目的是：1）确定线粒体功能增强对ECD的影响 肝移植，2）确定去除DAMP对移植后移植物损伤和功能的影响。