Mitogen-activated protein kinase-guided drug discovery for post-viral and related types of lung disease.

IF 9 1区 医学 Q1 RESPIRATORY SYSTEM
European Respiratory Review Pub Date : 2024-02-28 Print Date: 2024-01-31 DOI:10.1183/16000617.0220-2023
Michael J Holtzman, Yong Zhang, Kangyun Wu, Arthur G Romero
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引用次数: 0

Abstract

Respiratory viral infections are a major public health problem, with much of their morbidity and mortality due to post-viral lung diseases that progress and persist after the active infection is cleared. This paradigm is implicated in the most common forms of chronic lung disease, such as asthma and COPD, as well as other virus-linked diseases including progressive and long-term coronavirus disease 2019. Despite the impact of these diseases, there is a lack of small-molecule drugs available that can precisely modify this type of disease process. Here we will review current progress in understanding the pathogenesis of post-viral and related lung disease with characteristic remodelling phenotypes. We will also develop how this data leads to mitogen-activated protein kinase (MAPK) in general and MAPK13 in particular as key druggable targets in this pathway. We will also explore recent advances and predict the future breakthroughs in structure-based drug design that will provide new MAPK inhibitors as drug candidates for clinical applications. Each of these developments point to a more effective approach to treating the distinct epithelial and immune cell based mechanisms, which better account for the morbidity and mortality of post-viral and related types of lung disease. This progress is vital given the growing prevalence of respiratory viruses and other inhaled agents that trigger stereotyped progression to acute illness and chronic disease.

以丝裂原活化蛋白激酶为指导,发现治疗病毒后和相关类型肺病的药物。
呼吸道病毒感染是一个重大的公共卫生问题,其发病率和死亡率主要是由于病毒感染后肺部疾病造成的,这些疾病在活动性感染清除后仍在发展和持续。这种模式与哮喘和慢性阻塞性肺病等最常见的慢性肺部疾病以及其他与病毒有关的疾病(包括渐进性和长期的冠状病毒疾病)有关。尽管这些疾病影响巨大,但目前仍缺乏能精确改变这类疾病过程的小分子药物。在此,我们将回顾目前在了解具有特征性重塑表型的病毒后肺部疾病和相关肺部疾病的发病机制方面取得的进展。我们还将介绍这些数据如何导致丝裂原活化蛋白激酶(MAPK),特别是 MAPK13 成为这一途径中的关键药物靶点。我们还将探讨基于结构的药物设计方面的最新进展并预测未来的突破,这些突破将为临床应用提供新的 MAPK 抑制剂候选药物。所有这些进展都指向一种更有效的方法来治疗基于上皮细胞和免疫细胞的不同机制,这些机制更好地解释了病毒后肺病和相关类型肺病的发病率和死亡率。鉴于呼吸道病毒和其他吸入性病原体越来越普遍,引发急性病和慢性病的定型进展,这一进展至关重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European Respiratory Review
European Respiratory Review Medicine-Pulmonary and Respiratory Medicine
CiteScore
14.40
自引率
1.30%
发文量
91
审稿时长
24 weeks
期刊介绍: The European Respiratory Review (ERR) is an open-access journal published by the European Respiratory Society (ERS), serving as a vital resource for respiratory professionals by delivering updates on medicine, science, and surgery in the field. ERR features state-of-the-art review articles, editorials, correspondence, and summaries of recent research findings and studies covering a wide range of topics including COPD, asthma, pulmonary hypertension, interstitial lung disease, lung cancer, tuberculosis, and pulmonary infections. Articles are published continuously and compiled into quarterly issues within a single annual volume.
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