Jezela-Stanek Aleksandra, Chorostowska-Wynimko Joanna
Department of Genetics and Clinical Immunology, National Institute of Tuberculosis and Lung Diseases, Warszawa, Poland.
Adv Clin Exp Med. 2019 Sep;28(9):1257-1261. doi: 10.17219/acem/103668.
Alpha-1 antitrypsin (AAT) is an acute-phase protein with strong inhibitory activity towards proteolytic enzymes, mainly elastase but also trypsin, chymotrypsin and thrombin. The biological role of the protein and the effects of its deficiency have been subjects of scientific research for years, yet in many areas our knowledge remains incomplete. Alpha-1 antitrypsin deficiency (AATD), a defect in AAT synthesis and functionality, is one of the most frequently inherited genetic disorders among Caucasian populations. Its severe form is characterized by very low serum levels of AAT, and it most often affects the lungs (causing early-onset emphysema or chronic obstructive lung disease (COPD)) and/or liver (leading to jaundice and liver cirrhosis in children and adults). However, little is known about other possible clinical consequences of AAT deficiency. We discuss AAT's potential role in mechanisms regulating human fertility and gestation, with a particular emphasis on the clinical context and on indications for AATD diagnostic testing.
α1抗胰蛋白酶(AAT)是一种急性期蛋白,对蛋白水解酶具有强大的抑制活性,主要是弹性蛋白酶,但也包括胰蛋白酶、糜蛋白酶和凝血酶。该蛋白的生物学作用及其缺乏所产生的影响多年来一直是科研课题,但在许多领域我们的认识仍不完整。α1抗胰蛋白酶缺乏症(AATD)是AAT合成及功能方面的缺陷,是白种人群中最常见的遗传性疾病之一。其严重形式的特征是血清AAT水平极低,最常影响肺部(导致早发性肺气肿或慢性阻塞性肺疾病(COPD))和/或肝脏(导致儿童和成人出现黄疸和肝硬化)。然而,关于AAT缺乏的其他可能临床后果知之甚少。我们讨论了AAT在调节人类生育和妊娠机制中的潜在作用,特别强调了临床背景以及AATD诊断检测的指征。