Implications and Stability of Clinical and Molecular Phenotypes of Severe Asthma

严重哮喘临床和分子表型的意义和稳定性

• 批准号: 8680344
• 负责人: Sally E Wenzel
• 金额: $ 67.55万
• 依托单位: UNIVERSITY OF PITTSBURGH AT PITTSBURGH
• 依托单位国家: 美国
• 财政年份: 2011
• 资助国家: 美国
• 起止时间: 2011-08-09 至 2017-05-31
• 项目状态: 已结题
• 来源: https://reporter.nih.gov/project-details/8680344
• 关键词: Accounting; Adult; Asthma; Biological Markers; Bronchoalveolar Lavage; Cell physiology; Cells; Characteristics; Child; Childhood; Chymase; Clinical; Data; Epithelial; Epithelial Cells; Epithelium; Evaluation; Genetic; Genomics; Goals; Heterogeneity; Human; In Vitro; Inflammatory; Instruction; Link; Liquid substance; Long-Term Effects; Longitudinal Studies; Lung; Lymphocyte; Measurement; Measures; Messenger RNA; Minority; Molecular; Molecular Abnormality; Molecular Genetics; Molecular Profiling; Molecular Target; Outcome; Pathologic; Pathway interactions; Pattern; Pharmaceutical Preparations; Phenotype; Physiological; Plasma; Principal Investigator; Prostaglandin D2; Protocols documentation; Publishing; Respiratory physiology; Severities; Sputum; Submucosa; Symptoms; Time; Tryptase; clinical phenotype; cost; genome wide association study; improved; in vivo; innovation; mast cell; molecular phenotype; novel; response; treatment response

DESCRIPTION (provided by applicant): SARP l/ll recognized clinical/pathologic differences of severe asthma compared to milder asthma and identified distinct severe asthma phentoypes at baseline. Additional pathobiologic abnormalities were observed to occur in and across clusters which linked similarities in symptoms, exacerbation predilection, treatment response. Yet, nothing is understood regarding the stability of implications of these clinical or pathologic phenotypes. Published SARP II data show that chymase positive mast cells (MCTC) predominate in the submucosa and epithelium in severe asthma, with evidence for an altered activation status. Preliminary data suggest that a luminal MCTC mRNA signature and activation pattern even better differentiates symptomatic and exacerbation prone severe from milder asthma. This MC signature is present across at least 2 of the 3 predominant severe asthma clusters. However, the mechanisms behind these changes, the interaction of these MCs with epithelial/inflammatory cells and their long term effects (and stability) are poorly understood. The goals of this application are to establish a longitudinal protocol capable of identifying asthma phenotypes and their long term implications in both adults and children with asthma and severe asthma, as well as evaluating their stability. This longitudinal protocol will intersect with mechanistic studies which identify a MCTC molecular phenotype, relate it to genetic characteristics as well as short/long term cellular, clinical, physiologic and radiologic outcomes and then analyze its stability over time. Finally, the proposal will mechanistically determine the impact of this mast cell signature on human airway epithelial cells. This innovative combination of in vitro/in vivo mechanistic and longitudinal molecular and clinical phenotyping is highly likely to uncover new molecular targets for severe asthma. RELEVANCE (See instructions): Severe asthma, impacts a minority of asthmatics, but accounts for a majority of the costs. While treatment of asthma has improved, severe asthma remains problematic and poorly treated. The proposed studies will identify new/novel molecular pathways, link them to baseline and longitudinal clinical, physiologic and radiologic outcomes and assess their stability over time leading to new molecular targets for therapy.

描述（由申请人提供）：SARP I/II识别出重度哮喘与轻度哮喘相比的临床/病理学差异，并在基线时识别出不同的重度哮喘表型。观察到其他病理生物学异常发生在集群内和集群间，这些异常与症状、加重偏好、治疗反应的相似性有关。然而，关于这些临床或病理表型的影响的稳定性还不清楚。已发表的SARP II数据显示，糜酶阳性肥大细胞（MCTC）在重度哮喘的粘膜下层和上皮中占主导地位，有证据表明其活化状态发生了改变。初步数据表明，管腔MCTC mRNA签名和激活模式甚至可以更好地区分症状性和易加重的重度哮喘与轻度哮喘。这种MC特征存在于3种主要重度哮喘簇中的至少2种。然而，这些变化背后的机制，这些MC与上皮/炎症细胞的相互作用及其长期影响（和稳定性）知之甚少。本申请的目的是建立一个纵向方案，能够识别哮喘表型及其在成人和儿童哮喘和重度哮喘患者中的长期影响，并评估其稳定性。该纵向方案将与识别MCTC分子表型的机制研究交叉，将其与遗传特征以及短期/长期细胞、临床、生理和放射学结局相关，然后分析其随时间的稳定性。最后，该提案将机械地确定这种肥大细胞特征对人类气道上皮细胞的影响。这种体外/体内机制和纵向分子和临床表型的创新组合极有可能发现严重哮喘的新分子靶点。 相关性（见说明）：严重哮喘，影响少数哮喘患者，但占大多数的费用。虽然哮喘的治疗有所改善，但严重哮喘仍然存在问题，治疗不力。拟议的研究将确定新的/新型分子途径，将其与基线和纵向临床、生理和放射学结局联系起来，并评估其随时间的稳定性，从而为治疗提供新的分子靶点。