Department of Molecular Medicine, University of Pavia, Via Taramelli 3, 27100 Pavia, Italy.
Department of Pulmonology, Leiden University Medical Center, Albinusdreef 2, 2333 Leiden, The Netherlands.
Int J Mol Sci. 2021 Jan 21;22(3):1065. doi: 10.3390/ijms22031065.
As a known genetic cause of chronic obstructive pulmonary disease (COPD), alpha1-antitrypsin deficiency (AATD) can cause severe respiratory problems at a relatively young age. These problems are caused by decreased or absent levels of alpha1-antitrypsin (AAT), an antiprotease which is primarily functional in the respiratory system. If the levels of AAT fall below the protective threshold of 11 µM, the neutrophil-derived serine proteases neutrophil elastase (NE) and proteinase 3 (PR3), which are targets of AAT, are not sufficiently inhibited, resulting in excessive degradation of the lung parenchyma, increased inflammation, and increased susceptibility to infections. Because other therapies are still in the early phases of development, the only therapy currently available for AATD is AAT augmentation therapy. The controversy surrounding AAT augmentation therapy concerns its efficiency, as protection of lung function decline is not demonstrated, despite the treatment's proven significant effect on lung density change in the long term. In this review article, novel biomarkers of NE and PR3 activity and their use to assess the efficacy of AAT augmentation therapy are discussed. Furthermore, a series of seven synthetic NE and PR3 inhibitors that can be used to evaluate the specificity of the novel biomarkers, and with potential as new drugs, are discussed.
作为慢性阻塞性肺疾病 (COPD) 的已知遗传原因,α1-抗胰蛋白酶缺乏症 (AATD) 可导致相对年轻的患者出现严重的呼吸问题。这些问题是由 α1-抗胰蛋白酶 (AAT) 的水平降低或缺失引起的,AAT 是一种主要在呼吸系统中起作用的抗蛋白酶。如果 AAT 水平降至 11µM 的保护阈值以下,AAT 的靶标中性粒细胞衍生的丝氨酸蛋白酶弹性蛋白酶 (NE) 和蛋白酶 3 (PR3) 就不能被充分抑制,导致肺实质过度降解、炎症增加和增加易感性感染。由于其他疗法仍处于早期开发阶段,目前 AATD 唯一可用的治疗方法是 AAT 增强疗法。AAT 增强疗法的争议在于其效率,尽管该治疗方法已被证明对长期肺密度变化具有显著影响,但并未显示出对肺功能下降的保护作用。在这篇综述文章中,讨论了 NE 和 PR3 活性的新型生物标志物及其在评估 AAT 增强疗法疗效中的应用。此外,还讨论了一系列可用于评估新型生物标志物特异性的七种合成 NE 和 PR3 抑制剂,并具有作为新药的潜力。