首页> 外文期刊>Disease models & mechanisms: DMM >From bedside to bench to clinic trials: identifying new treatments for severe asthma
【24h】

From bedside to bench to clinic trials: identifying new treatments for severe asthma

机译:从床旁到长凳再到临床试验:确定重度哮喘的新疗法

获取原文
       

摘要

Asthmatics with a severe form of the disease are frequently refractory to standard medications such as inhaled corticosteroids, underlining the need for new treatments to prevent the occurrence of potentially life-threatening episodes. A major obstacle in the development of new treatments for severe asthma is the heterogeneous pathogenesis of the disease, which involves multiple mechanisms and cell types. Furthermore, new therapies might need to be targeted to subgroups of patients whose disease pathogenesis is mediated by a specific pathway. One approach to solving the challenge of developing new treatments for severe asthma is to use experimental mouse models of asthma to address clinically relevant questions regarding disease pathogenesis. The mechanistic insights gained from mouse studies can be translated back to the clinic as potential treatment approaches that require evaluation in clinical trials to validate their effectiveness and safety in human subjects. Here, we will review how mouse models have advanced our understanding of severe asthma pathogenesis. Mouse studies have helped us to uncover the underlying inflammatory mechanisms (mediated by multiple immune cell types that produce Th1, Th2 or Th17 cytokines) and non-inflammatory pathways, in addition to shedding light on asthma that is associated with obesity or steroid unresponsiveness. We propose that the strategy of using mouse models to address clinically relevant questions remains an attractive and productive research approach for identifying mechanistic pathways that can be developed into novel treatments for severe asthma.
机译:具有严重疾病形式的哮喘患者通常对诸如吸入性皮质类固醇的标准药物难以治疗,从而强调需要采取新的治疗方法来预防可能危及生命的发作。开发用于重度哮喘的新疗法的主要障碍是该疾病的异质发病机制,其涉及多种机制和细胞类型。此外,可能需要将新疗法针对其疾病发病机制由特定途径介导的患者亚组。解决针对重度哮喘开发新疗法的挑战的一种方法是使用哮喘的实验小鼠模型来解决有关疾病发病机理的临床相关问题。从小鼠研究中获得的机械学见解可以转化为临床,作为需要在临床试验中进行评估以验证其在人类受试者中的有效性和安全性的潜在治疗方法。在这里,我们将回顾小鼠模型如何增进我们对严重哮喘发病机理的了解。小鼠研究帮助我们发现了潜在的炎症机制(由产生Th1,Th2或Th17细胞因子的多种免疫细胞类型介导)和非炎症途径,以及减轻了与肥胖症或类固醇无反应性有关的哮喘。我们建议使用小鼠模型来解决临床相关问题的策略仍然是一种有吸引力的且富有成果的研究方法,用于识别可以发展为重度哮喘的新疗法的机制途径。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号