University of Catania-AOU Policlinico-V. Emanuele, Institute of Internal Medicine and Clinical Immunology, Department of Clinical and Molecular Bio-Medicine, Catania, Italy.
Expert Opin Ther Targets. 2013 Jul;17(7):761-72. doi: 10.1517/14728222.2013.795220. Epub 2013 May 4.
Adenosine receptors (ARs) and their differential pattern of expression modulate a series of pleiotropic activities that are known to contribute to the control of inflammation, remodeling, and tissue repair. Consequently, pharmacological manipulation of adenosine signaling pathway is of great interest and is currently exploited as a therapeutic target for a number of respiratory diseases with several molecules with agonist and antagonist activities against known ARs being developed for the treatment of different conditions of the respiratory system.
Herein, we will review the rational basis leading to the development of novel therapies for asthma, chronic obstructive pulmonary disease (COPD), interstitial lung disease (ILD), pulmonary arterial hypertension (PAH), and cystic fibrosis. Their most recent clinical development will be also discussed.
Advances in our understanding of the pathogenetic role of adenosine in respiratory diseases may be soon translated into effective treatment options. In consideration of the complex interplay driven by the different pattern of receptor distribution and/or affinity of the four known AR subtypes in specific cell types at different stages of the disease, it is likely that combination of selective antagonist/agonists for different AR subtypes will be required to obtain reasonable clinical efficacy. Alternatively, controlling the factors involved in driving adenosine concentrations in the tissue may be also of great significance.
腺苷受体(ARs)及其表达模式的差异调节了一系列多效性活动,这些活动已知有助于控制炎症、重塑和组织修复。因此,对腺苷信号通路的药理学干预具有重要意义,目前正被用作许多呼吸系统疾病的治疗靶点,许多具有激动剂和拮抗剂活性的分子被开发用于治疗呼吸系统的不同疾病。
本文将综述导致新型哮喘治疗方法、慢性阻塞性肺疾病(COPD)、间质性肺病(ILD)、肺动脉高压(PAH)和囊性纤维化发展的合理基础。还将讨论它们最近的临床进展。
我们对腺苷在呼吸系统疾病中的发病机制作用的理解的进步可能很快就会转化为有效的治疗选择。考虑到不同疾病阶段特定细胞类型中四种已知 AR 亚型的受体分布和/或亲和力的不同模式驱动的复杂相互作用,很可能需要联合使用不同 AR 亚型的选择性拮抗剂/激动剂来获得合理的临床疗效。或者,控制驱动组织中腺苷浓度的因素也可能具有重要意义。