Contribution of TNF-alpha to mucus cell production in asthma
Contribution of TNF-alpha to mucus cell production in asthma
批准号:
7248709
负责人:
PAULA J BUSSE
金额:
$11.33万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-07-01 至 2011-05-31
关键词:
Adrenal Cortex HormonesAnimal ModelAnti-Inflammatory AgentsAnti-inflammatoryAntibodiesArginineAsthmaAttenuatedBasement membraneBindingCell LineCellsChronicCollagenDepositionDiseaseEpithelial CellsExhalationExtracellular ProteinExtrinsic asthmaGene ExpressionGenesGenetic TranscriptionGoalsGoblet CellsHumanHyperplasiaHypertrophyIn VitroInflammationInflammatoryInterleukin-4LeadMetaplasiaModelingMonoclonal AntibodiesMucinsMucous body substanceMusNF-kappa BNOS2A geneNeuronsNitric OxideNitric Oxide SynthaseNumbersObstructionPathologyPathway interactionsPatientsProductionPropertyRegulationResearch PersonnelRoleSecondary toSystemT-LymphocyteTherapeuticThickTumor Necrosis Factor ReceptorTumor Necrosis Factor-alphaUp-RegulationWorkairway inflammationairway remodelingasthmatic patientcytokinehuman NOS2A proteinhuman TNF proteinin vivomRNA Expressionmast celloxidationpreventprogramsrespiratoryrespiratory smooth muscleresponse
中文摘要
描述(由申请人提供):哮喘是一种炎症性气道疾病,通常以可逆性梗阻为特征。然而,在某些患者中,这种炎症可导致继发于结构改变的不可逆阻塞。这些气道改变包括粘液细胞增生/肥大,胶原和其他细胞外蛋白沉积导致气道基底膜厚度增加,血管扩张,神经元反应改变和气道平滑肌肥大。目前的证据表明,这些变化可能无法通过抗炎治疗如皮质类固醇来预防,但这是有争议的。TNF-a在哮喘中是一种重要的细胞因子,具有促炎和促纤维化的特性,其在促进气道结构变化中的作用已在哮喘动物模型和人类中被注意到。重要的是,阻断TNF-a作用的方法已被证明在许多其他慢性炎症性疾病中相当有效。在此背景下,笔者假设TNF-a是哮喘中调节黏液细胞增生的重要细胞因子。此外,使用抗TNF-a抗体调节TNF-a可能是哮喘的一种适当的辅助治疗,可以预防或减轻黏液细胞增生/肥大(小鼠系统中的化生),并避免长期使用皮质类固醇的后果。本提案的总体目标是评估TNF-a对哮喘气道病理的一个重要方面的影响,即黏液细胞增生/肥大。
英文摘要
DESCRIPTION (provided by applicant): Asthma is an inflammatory airways disease which is often characterized by reversible obstruction. In certain patients, however, this inflammation may lead to irreversible obstruction, secondary to structural changes. These airway changes include mucus cell hyperplasia/hypertrophy, increased thickness of the airway basement membrane by deposition of collagen and other extracellular proteins, increased vascularity, altered neuronal responses and hypertrophy of the airway smooth muscle. Current evidence suggests that these changes may not be prevented with anti-inflammatory treatment such as corticosteroids, but this is controversial. TNF-a is an important cytokine in asthma which has both proinflammatory and profibrotic properties and its role in promoting structural changes in the airway has been noted in animal models of asthma and in humans. Importantly, approaches to block the effects of TNF-a have proven to be quite effective in a number of other chronic inflammatory diseases. Given this background, it is my hypothesis that TNF-a is an important cytokine in asthma in the regulation of mucus-cell hyperplasia. Furthermore, modulation of TNF-a, using an anti-TNF-a antibody may be an appropriate adjunctive therapy in asthma, preventing or attenuating mucus-cell hyperplasia/hypertrophy (metaplasia in the murine system) and avoiding the consequences of long-term corticosteroid use. The overall goal of this proposal is to evaluate the effects of TNF-a on an important aspect of airway pathology in asthma, mucus-cell hyperplasia/hypertrophy.
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