基于新的2型高和2型低内分型的哮喘表型分类:这一切都始于Rackemann

J. Bellanti
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引用次数: 1

摘要

背景:哮喘现在被认为是一种异质性的疾病实体集合,与不同的临床表型表现和不同的内型机制相关。最近,一种新的哮喘命名系统通过使用2型(T2)高和T2低的内型分类而发展起来,这种分类已被证明有助于诊断和为哮喘患者选择正确的生物制剂。目的:本报告的目的是提供分子内型、哮喘表型和现有生物标志物的概述,重点关注在Francis M. Rackemann医学博士贡献的历史背景下T2和非T2途径的新分类系统,这为我们目前对哮喘疾病实体谱的理解奠定了基础,并为使用新兴生物制剂治疗这些疾病奠定了基础。方法:根据PubMed的文献综述,结合作者本人的研究和临床经验。结果:目前,哮喘的治疗是基于患者特异性表型特征和潜在的组织损伤内源性机制的治疗策略,重点是t2 -高和t2 -低气道炎症分类。基于这一分类,临床医生可以为哮喘患者的个性化护理选择合适的生物制剂提供有用的治疗策略。虽然它的整体适用性并不完美,但它提供了一个指南,帮助在当前可用的生物制剂中选择最合适的生物制剂,以及那些不可避免地会成为可用的生物制剂。结论:本报告中描述的哮喘表型分类始于一位精明的临床医生的临床观察,这些观察早在与t2 -高和t2 -低免疫功能相关的信息超新星出现之前就开始了。拉克曼对临床过敏实践的贡献再次说明,科学和技术可以通过临床观察的激励力量得到最好的进步。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Phenotypic classification of asthma based on a new Type 2‐high and Type 2‐low endotypic classification: It all began with Rackemann
Background: Asthma is now recognized as a heterogeneous collection of disease entities associated with different clinical phenotypic presentations and diverse endotypic mechanisms. Recently, a new system of nomenclature of asthma has evolved by using a type 2 (T2) high and T2-low endotypic classification that has proven useful for diagnosis and for choosing the right biologic for patients with asthma. Aim: The purpose of this report was to provide an overview of molecular endotypes, asthma phenotypes, and existing biomarkers, with a focus on the new classification system of T2 and non-T2 pathways in the historical context of the contributions of Francis M. Rackemann, M.D., that set the stage both for our current understanding of the spectrum of disease entities of asthma and for the basis for the use of emerging biologics for the treatment of these disorders. Methods: This article was based on literature review of PubMed and the author’s own research and clinical experiences. Results: Currently, the therapy for asthma is being directed to a treatment strategy based on patient-specific phenotypic characteristics and underlying endotypic mechanisms of tissue injury that focus on a T2-high and T2-low airway inflammation classification. Based on this classification, the clinician is provided with a useful treatment stratagem for choosing the right biologic for personalized care of patients with asthma. Although not perfect in its total applicability, it affords a guide in helping to choose among the currently available biologics, the most appropriate one, as well as those that inevitably will become available. Conclusion: The phenotypic classification of asthma described in this report began with the clinical observations that were made by of an astute clinician long before the supernova emergence of information related to T2-high and T2-low immune function. Rackemann’s legacy to clinical allergy practice once again illustrates that science and technology can best progress through the energizing force of clinical observation.
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