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首页> 外文期刊>Annals of allergy, asthma, and immunology >Allergic and eosinophilic asthma in the era of biomarkers and biologics: similarities, differences and misconceptions: Similarities, differences, and misconceptions
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Allergic and eosinophilic asthma in the era of biomarkers and biologics: similarities, differences and misconceptions: Similarities, differences, and misconceptions

机译:生物标志物和生物制剂时代的过敏性和嗜酸性粒细胞性哮喘:相似之处、不同之处和误解:相似之处、不同之处和误解

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? 2022 The AuthorsObjective: Severe asthma is associated with substantial personal and economic burden; maintaining disease control is the key management goal. Increased understanding of asthma heterogeneity and development of type 2 (T2)-targeting biologics has substantially advanced disease management and outcomes; however, despite both being driven by T2 inflammation, allergic and eosinophilic asthma have different treatment recommendations. We sought to better understand the similarities and differences between allergic and eosinophilic asthma and highlight where misconceptions may arise. Data Sources: Published articles, pivotal trials, post hoc analyses, and asthma clinical guidelines sourced from PubMed. Study Selections: Sources reporting allergic and eosinophilic asthma classifications, disease mechanisms, and biomarkers associated with treatment response. Results: This review highlights that severe allergic and eosinophilic asthma are both driven by T2 inflammation with eosinophils playing a cardinal role. Despite this overlap, treatment recommendations differ based on asthma classification. T2 cytokine gene expression is a reasonably well-established research tool, but not a well-established biomarker in clinical practice, unlike blood eosinophil counts, fractional exhaled nitric oxide, and immunoglobulin E; the clinical relevance of immunoglobulin E as a predictive biomarker remains unclear. Conclusion: Asthma classifications that can be easily characterized at patient level to ensure accurate diagnosis, predict disease trajectory, and treatment response are required. The current dichotomy of allergic and eosinophilic asthma classifications is likely too simplistic, given the similar eosinophil-mediated disease pathophysiology in both classifications. Our results provide future directions to guide clinically meaningful interpretation of asthma endophenotypes, which may improve understanding of severe asthma characterization and aid future advances in defining responders more precisely with personalized medicine approaches.
机译:?2022 作者目标:严重的哮喘与巨大的个人和经济负担有关;保持疾病控制是关键的管理目标。对哮喘异质性的认识和 2 型 (T2) 靶向生物制剂的开发大大推动了疾病管理和结果;然而,尽管两者都是由 T2 炎症驱动的,但过敏性和嗜酸性粒细胞性哮喘有不同的治疗建议。我们试图更好地了解过敏性哮喘和嗜酸性粒细胞性哮喘之间的异同,并强调可能出现误解的地方。数据来源:已发表的文章、关键性试验、事后分析和哮喘临床指南,来源于 PubMed。研究选择:报告过敏性和嗜酸性粒细胞性哮喘分类、疾病机制以及与治疗反应相关的生物标志物的来源。结果:本综述强调,严重过敏性哮喘和嗜酸性粒细胞性哮喘都是由T2炎症驱动的,其中嗜酸性粒细胞起着主要作用。尽管存在这种重叠,但治疗建议因哮喘分类而异。T2 细胞因子基因表达是一种相当成熟的研究工具,但在临床实践中并不是一个成熟的生物标志物,这与血液嗜酸性粒细胞计数、呼出气一氧化氮分数和免疫球蛋白 E 不同;免疫球蛋白E作为预测性生物标志物的临床相关性尚不清楚。结论:需要在患者水平上轻松表征哮喘分类,以确保准确诊断、预测疾病轨迹和治疗反应。目前过敏性哮喘和嗜酸性粒细胞性哮喘的二分法可能过于简单化,因为这两种分类中嗜酸性粒细胞介导的疾病病理生理学相似。我们的研究结果为指导哮喘内表型的临床有意义的解释提供了未来的方向,这可能会提高对严重哮喘特征的理解,并有助于未来通过个性化医学方法更精确地定义反应者的进展。

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