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哮喘的新型疗法——进展与问题

Novel therapies for asthma--advances and problems.

作者信息

Walsh Garry M

机构信息

Asthmatic & Allergic Inflammation Group, School of Medicine, Institute of Medical Sciences, University of Aberdeen, Foresterhill, Aberdeen, AB25 2ZD, UK.

出版信息

Curr Pharm Des. 2005;11(23):3027-38. doi: 10.2174/1381612054864984.

Abstract

It is now widely accepted that airway inflammation is the key factor underlying the pathogenesis of asthma. While corticosteroids remain the most important anti-inflammatory treatment for asthma they are rather non-specific in their actions. Their use also raises concerns over side effects and compliance issues, particularly in children and adolescents. There is therefore much effort being made to develop novel more specific and safer therapy for asthma. Efforts are being made to improve existing drugs together with the use of combination therapy with anti-histamines and leukotriene antagonists. An important area for potential advances in glucocorticoid (GC) development include the elucidation of the crystal structure of the GC receptor ligand-binding domain that may provide vital information in dissociating the anti-inflammatory effects of GCs from unwanted side-effects. Other areas include the development of humanised monoclonal antibodies for asthma therapy including those against IgE, IL-4 and IL-5 together with the inhibition of adhesion pathways and/or chemokines responsible for inflammatory cell accumulation in the asthmatic lung. The potential for immunotherapy using T cell peptide epitopes or DNA-based vaccines and the use of anti-inflammatory cytokines such as IL-10 or IFN-gamma are discussed. Several avenues of research are currently underway in an attempt to define mechanisms by which pro-inflammatory cells such as eosinophils can be safely removed from the asthmatic lung through apoptosis induction and their subsequent ingestion by phagocytes. Novel strategies include elucidation of the intracellular pathways controlling granulocyte apoptosis and the receptor mediated events employed by macrophages and bronchial epithelial cells in the recognition and removal of apoptotic cellular corpses. This paper will provide an overview of both the potential and shortcomings of these diverse approaches to drug development for asthma.

摘要

目前人们广泛认为气道炎症是哮喘发病机制的关键因素。虽然皮质类固醇仍然是哮喘最重要的抗炎治疗药物,但它们的作用相当非特异性。其使用也引发了对副作用和依从性问题的担忧,尤其是在儿童和青少年中。因此,人们正在努力开发针对哮喘的新型、更具特异性和安全性的疗法。人们正在努力改进现有药物,并结合使用抗组胺药和白三烯拮抗剂进行联合治疗。糖皮质激素(GC)开发潜在进展的一个重要领域包括阐明GC受体配体结合域的晶体结构,这可能为区分GC的抗炎作用与不良副作用提供关键信息。其他领域包括开发用于哮喘治疗的人源化单克隆抗体,包括针对IgE、IL-4和IL-5的抗体,以及抑制负责哮喘肺部炎症细胞积聚的黏附途径和/或趋化因子。还讨论了使用T细胞肽表位或基于DNA的疫苗进行免疫治疗的潜力,以及使用抗炎细胞因子如IL-10或IFN-γ的潜力。目前正在进行几条研究途径,试图确定通过诱导凋亡并随后由吞噬细胞摄取,将嗜酸性粒细胞等促炎细胞从哮喘肺部安全清除的机制。新策略包括阐明控制粒细胞凋亡的细胞内途径,以及巨噬细胞和支气管上皮细胞在识别和清除凋亡细胞尸体时采用的受体介导事件。本文将概述这些不同的哮喘药物开发方法的潜力和缺点。

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