IMMUNOPATHOLOGICAL ASPECTS OF THREMAL INJURY

热损伤的免疫病理学方面

• 批准号: 7317594
• 负责人: MARTIN G SCHWACHA
• 金额: $ 5.02万
• 依托单位: UNIVERSITY OF ALABAMA AT BIRMINGHAM
• 依托单位国家: 美国
• 财政年份: 2007
• 资助国家: 美国
• 起止时间: 2007-09-01 至 2008-04-30
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/7317594
• 关键词: Anti-Inflammatory Agents; Anti-inflammatory; Biological Response Modifier Therapy; Blood; Burn injury; Cells; Characteristics; Clinical; Complex; Condition; Critical Illness; Data; Dermal; Development; Distal; Equilibrium; Excision; Growth Factor; Healed; Human; Immune; Immune System Diseases; Immunosuppression; Impaired wound healing; Implant; Infection; Infiltration; Inflammation; Inflammatory; Inflammatory Response; Injury; Institutes; Laboratories; Leukocytes; Link; Mediating; Mediator of activation protein; Morbidity - disease rate; Multiple Organ Failure; Mus; Myeloid Cells; Nitric Oxide; Numbers; Operative Surgical Procedures; Organ; Patient Care; Patients; Phase; Phenotype; Play; Population; Porifera; Positioning Attribute; Predisposition; Process; Production; Pseudomonas aeruginosa; Range; Recovery; Regulation; Research Personnel; Residual state; Role; Sampling; Sepsis; Series; Severities; Site; Skin; Skin graft; Staging; Surgical complication; T-Cell Receptor; T-Lymphocyte; T-Lymphocyte Subsets; Techniques; Therapeutic; Therapeutic immunosuppression; Time; Tissues; Wound Healing; cell type; concept; cytokine; healing; heat injury; human NOS2A protein; immunopathology; improved; injured; insight; macrophage; migration; model development; neutrophil; novel; programs; research study; response; septic; wound

DESCRIPTION (provided by applicant): Major thermal injury induces a pathophysiological response that has a marked inflammatory/immune component which contributes to numerous complications that include delayed wound healing, increased susceptibility to sepsis and multiple organ failure. A wide range of mediators and cell types closely regulate the post-burn inflammatory process. Nonetheless, the ability of the burn patient to maintain an appropriate balance between inflammatory and anti-inflammatory responses following major burn injury is often disrupted leading to immunopathological complications. In this regard, a unique T-cell subset, gamma delta (7/8) T- cells has the ability to regulate inflammatory and healing processes. Gamma/delta T-cells are likely to be a critical component of the patient's successful recovery from burn injury. Our recent findings support an important multi-faceted role for y/8 T-cells in post-burn immunopathology by demonstrating the following: they are mobilized and activated early post-injury; they regulate post-burn neutrophil migration and; 7/8 T- cells contribute to burn wound healing via the regulation of growth factor, cytokine, and nitric oxide (NO) production at the injury site. While macrophage NO production (which is regulated by y/8 T-cells under certain conditions) is an important mediator of post-burn immune dysfunction, it is also critical to many aspects of wound repair. Burn injury is first and foremost an injury to the skin and a vast majority of burn patients have complications related to healing of the burn or skin graft site. Nonetheless, while y/8 T-cells are important to wound healing, their role in such processes post-burn remains to be clearly elucidated. It is our hypothesis that y/8 T-cells play a critical regulatory role in the post-burn dermal inflammatory response and wound healing that is, in part, mediated by an iNOS-dependent mechanism. The specific aims will determine: 1) the role of y/8 T-cells in post-burn wound healing and the dermal inflammatory response; 2) the role of y/8 T-cells in burn excision and grafting and; 3) the relationship of y/8 T-cells to the post burn wound healing and inflammatory responses in humans. Elucidation of the relationships between y/8 T-cells, the dermal inflammatory response and post-burn wound healing will be vital in the development of improved therapeutic regimes for this critically ill patient population, which could include the novel concept of biotherapy with y/8 T-cells or modulation of native y/8 T-cell activity.

描述(申请人提供)：严重的热损伤引起的病理生理反应具有显著的炎症/免疫成分，导致许多并发症，包括延迟伤口愈合、增加对脓毒症和多器官衰竭的易感性。多种介质和细胞类型密切调控着烧伤后的炎症过程。然而，烧伤患者在严重烧伤后维持炎症反应和抗炎反应之间的适当平衡的能力经常被破坏，导致免疫病理并发症。在这一点上，一个独特的T细胞亚群，伽马三角洲(7/8)T细胞具有调节炎症和愈合过程的能力。伽马/德尔塔T细胞很可能是患者成功从烧伤中恢复的关键组成部分。我们最近的发现支持了Y/8 T细胞在烧伤后免疫病理中的重要作用，证明了以下几点：它们在烧伤后早期被动员和激活；它们调节烧伤后中性粒细胞的迁移；7/8 T细胞通过调节创面生长因子、细胞因子和一氧化氮(NO)的产生而促进烧伤创面的愈合。虽然巨噬细胞NO的产生(在一定条件下由Y/8 T细胞调节)是烧伤后免疫功能障碍的重要介质，但它在创面修复的许多方面也是至关重要的。烧伤首先是对皮肤的损伤，绝大多数烧伤患者都有与烧伤愈合或植皮部位相关的并发症。尽管如此，尽管Y/8 T细胞对创面愈合很重要，但它们在烧伤后这种过程中的作用仍有待明确阐明。我们的假设是，Y/8T细胞在烧伤后真皮炎症反应和创面愈合中起着关键的调节作用，这在一定程度上是由iNOS依赖的机制介导的。这些具体目标将决定：1)Y/8 T细胞在烧伤后创面愈合和真皮炎症反应中的作用；2)Y/8 T细胞在烧伤切除和移植中的作用；3)Y/8 T细胞与人类烧伤后创面愈合和炎症反应的关系。阐明y/8T细胞、真皮炎性反应和烧伤后创面愈合之间的关系对于改进这一危重患者的治疗方案将是至关重要的，这可能包括用y/8T细胞进行生物治疗的新概念或调节天然y/8T细胞活性。