Viral-Driven Mediators of Chronic Lung Allograft Dysfunction

慢性肺同种异体移植功能障碍的病毒驱动介质

• 批准号: 7446602
• 负责人: MICHAEL J WALTER
• 金额: $ 36.9万
• 依托单位: WASHINGTON UNIVERSITY
• 依托单位国家: 美国
• 财政年份: 2006
• 资助国家: 美国
• 起止时间: 2006-07-14 至 2010-06-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7446602
• 关键词: Allografting; Antibodies; Appendix; Attenuated; Bone Marrow; Bronchiolitis Obliterans; Bronchoalveolar Lavage; Cells; Cessation of life; Chemotactic Factors; Chronic; Chronic Disease; Chronic lung disease; Cohort Studies; Collagen; Common Cold; Condition; Deposition; Development; Disease; Epithelial; Epithelial Cells; Functional disorder; Goals; Homologous Transplantation; Human; Immune; Immune response; Infectious Agent; Inflammation; Inflammatory; Inflammatory Response; Injury; Interleukin-12; Knowledge; Life; Link; Lung; Lung Transplantation; Lung diseases; Mediating; Mediator of activation protein; Modeling; Morbidity - disease rate; Mouse Strains; Mus; Onset of illness; Patients; Pattern; Phenotype; Protein Overexpression; Proteins; Regression Analysis; Request for Applications; Research; Research Personnel; Respiratory Failure; Risk; Risk Factors; Role; Staging; Syndrome; Therapeutic; Transplant Recipients; Transplantation; Viral; Viral Bronchiolitis; Virus; Virus Diseases; abstracting; airway inflammation; base; cell injury; cohort; cytokine; insight; lung allograft; macrophage; mortality; mouse model; novel; pathogen; prevent; programs; prospective; research study; respiratory; response; response to injury

DESCRIPTION (provided by applicant): Bronchiolitis obliterans (BO) following lung transplantation is a chronic disease associated with increased morbidity and mortality. The disease results in progressive respiratory failure and is characterized by airway epithelial cell injury, airway inflammation and fibrous obliteration of the airway lumen. We have recently demonstrated antecedent respiratory viral infection is a distinct risk factor for the subsequent development of death and bronchiolitis obliterans syndrome (BOS), the functional manifestation of BO. Our long-term research objective is to examine the role of airway epithelial cell injury-response cytokines in mediating viral-dependent allograft dysfunction. For this application, we propose respiratory viral infection of the allograft results in enhanced epithelial cell injury and increased expression of epithelial injury-response cytokines. In turn, these injury-response cytokines initiate inflammatory cascades that culminate in allograft dysfunction. To investigate this proposal, we examined the role of respiratory viral infection in a mouse transplant model. Respiratory viral infection in combination with transplantation resulted in allograft dysfunction manifested as exaggerated epithelial injury, macrophage- predominant inflammation and fibrous obliteration of the allograft. We next demonstrated viral infection and transplantation resulted in a synergistic increase in the expression of the epithelial cell injury-response cytokine IL-12 p80 (p80), a macrophage chemoattractant. Additional experiments using mouse strains that enhanced or blocked p80 function confirmed p80 was a central effector of allograft dysfunction. Collectively, these results suggested expression of p80 may also mediate allograft dysfunction in humans. In support of this possibility, transplant recipients with excessive airway inflammation, a known risk factor for subsequent BOS, demonstrated elevated bronchoalveolar lavage levels of p80 that correlated with increased macrophage accumulation in the allograft. Accordingly, the aims of this proposal are to determine the effects of p80 in viral-dependent allograft dysfunction, determine the role of p80 on the immune response in viral-dependent allograft dysfunction, and perform a prospective cohort study of human lung transplant recipients to characterize the role for viral-driven p80 expression in BOS. These studies will provide insight into the viral-dependent pathophysiologic mechanisms that result in chronic allograft dysfunction, and exploitation of this knowledge may be used to identify therapeutic strategies aimed to prevent disease onset or delay its progression. In lay terms, we have previously shown that the common cold, or a respiratory viral infection, is associated with chronic lung disease in people that have had a lung transplant. In particular, these viral infections increase the risk of chronic lung rejection and death. This research will study how these viruses cause chronic lung rejection so that treatments for this condition can be developed. (End of Abstract)

描述（由申请人提供）： 肺移植后闭塞性细支气管炎（BO）是一种慢性疾病，与发病率和死亡率增加有关。该疾病导致进行性呼吸衰竭，其特征在于气道上皮细胞损伤、气道炎症和气道腔的纤维闭塞。我们最近证实，先前的呼吸道病毒感染是随后发生死亡和闭塞性细支气管炎综合征（BOS）（BO的功能表现）的一个明显危险因素。我们的长期研究目标是检测气道上皮细胞损伤反应细胞因子在介导病毒依赖性同种异体移植物功能障碍中的作用。对于这种应用，我们提出呼吸道病毒感染的同种异体移植物的结果在增强上皮细胞损伤和上皮损伤反应细胞因子的表达增加。反过来，这些损伤反应细胞因子启动炎症级联反应，最终导致同种异体移植物功能障碍。为了研究这一建议，我们研究了呼吸道病毒感染在小鼠移植模型中的作用。呼吸道病毒感染联合移植导致移植物功能障碍，表现为过度的上皮损伤、巨噬细胞为主的炎症和移植物的纤维闭塞。我们接下来证明了病毒感染和移植导致上皮细胞损伤反应细胞因子IL-12 p80（p80）（一种巨噬细胞化学引诱物）表达的协同增加。使用增强或阻断p80功能的小鼠品系进行的其他实验证实了p80是同种异体移植物功能障碍的中心效应子。总的来说，这些结果表明p80的表达也可能介导人类同种异体移植物功能障碍。为了支持这种可能性，移植受者过度气道炎症，一个已知的风险因素，随后BOS，表现出支气管肺泡灌洗水平升高的p80与增加的巨噬细胞在同种异体移植物中的积累。因此，本提案的目的是确定p80在病毒依赖性同种异体移植物功能障碍中的作用，确定p80在病毒依赖性同种异体移植物功能障碍中对免疫应答的作用，并对人肺移植受者进行前瞻性队列研究，以表征病毒驱动的p80表达在BOS中的作用。这些研究将深入了解导致慢性同种异体移植物功能障碍的病毒依赖性病理生理机制，利用这些知识可用于确定旨在预防疾病发作或延迟其进展的治疗策略。 通俗地说，我们以前已经表明，普通感冒或呼吸道病毒感染与肺移植患者的慢性肺病有关。特别是，这些病毒感染增加了慢性肺排斥反应和死亡的风险。这项研究将研究这些病毒如何引起慢性肺排斥反应，以便开发这种疾病的治疗方法。(End摘要）