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从表型到内型再到哮喘治疗。

From phenotypes to endotypes to asthma treatment.

机构信息

Faculty of Medicine, Department of Allergy and Clinical Immunology, Transylvania University Brasov, Brasov, Romania.

出版信息

Curr Opin Allergy Clin Immunol. 2013 Jun;13(3):249-56. doi: 10.1097/ACI.0b013e32836093dd.

Abstract

PURPOSE OF REVIEW

The current guidelines for asthma diagnosis and management do not recognize that different phenotypes of asthma exist, with significant variations in the manifestation of airway inflammation, symptoms, severity, and response to treatment. This article will critically review new approaches to classify asthma together with the emerging endotype-driven therapeutic strategies.

RECENT FINDINGS

Several new approaches for classifying asthma are available, from precision and deep phenotyping to identification of novel causal pathways and translation of biomarkers into pathway-specific diagnostic tests. New phenotypes, such as epigenetic phenotypes, asthmatic granulomatosis, or neurophenotypes are described. Large clinical trials testing the endotype-driven approach are increasingly successful, but the dissociated effect and the drug efficacy at the target site remain unsolved issues. Profiling the Th2 low and the resident cell compartment of asthma are major unmet needs in asthma endotyping.

SUMMARY

Each of the hallmark characteristics of asthma (inflammation, remodeling, airway hyperreactivity) is the expression of a complex network of molecules, very diverse both within any given patient in time and between any two patients. Some of these networks are repetitive across individuals with asthma and specific for clinical expression, gene-environment interaction and inflammatory cell profiles represent novel endotype-specific diagnostic and therapeutic strategies.

摘要

目的综述

目前的哮喘诊断和管理指南并未认识到存在不同的哮喘表型,气道炎症、症状、严重程度和治疗反应表现存在显著差异。本文将批判性地回顾哮喘分类的新方法以及新兴的基于表型的治疗策略。

最近的发现

目前有多种新的哮喘分类方法,包括精准和深度表型分析、确定新的因果途径以及将生物标志物转化为针对特定途径的诊断测试。描述了新的表型,如表观遗传表型、哮喘性肉芽肿或神经表型。越来越多的大型临床试验正在测试基于表型的方法,但靶点药物疗效和脱靶效应仍是未解决的问题。在哮喘表型分析中,Th2 低反应和固有细胞群仍有未满足的需求。

总结

哮喘的每个标志性特征(炎症、重塑、气道高反应性)都是一个复杂分子网络的表达,无论是在任何特定患者的时间内还是在任何两个患者之间,这些分子网络都非常多样化。这些网络中的一些在哮喘患者中具有重复性,并且与临床表型、基因-环境相互作用和炎症细胞特征特异性相关,代表了新的基于表型的诊断和治疗策略。

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