Perlmutter D H
Departments of Pediatrics, Biology, and Physiology, Washington University School of Medicine, St. Louis, Missouri, USA.
Clin Liver Dis. 2000 May;4(2):387-408, vi. doi: 10.1016/s1089-3261(05)70115-x.
Alpha 1-antitrypsin deficiency is the most common genetic cause of liver disease in children. It is also associated with chronic liver disease, hepatocellular carcinoma, and pulmonary emphysema in adults. Liver injury is caused by hepatotoxic effects of retention of the mutant alpha 1-antitrypsin molecule within the endoplasmic reticulum of liver cells, and emphysema is caused by uninhibited proteolytic damage to elastic tissue in the lung parenchyma. Recent studies of the biochemistry and cell biology of the mutant alpha 1-antitrypsin molecule have led to advances in understanding susceptibility to liver injury and in developing new strategies for prevention of both liver and lung disease.
α1-抗胰蛋白酶缺乏症是儿童肝病最常见的遗传病因。它还与成人的慢性肝病、肝细胞癌和肺气肿有关。肝损伤是由突变的α1-抗胰蛋白酶分子滞留在肝细胞内质网内产生的肝毒性作用引起的,而肺气肿是由肺实质弹性组织不受抑制的蛋白水解损伤引起的。最近对突变的α1-抗胰蛋白酶分子的生物化学和细胞生物学研究,在理解肝损伤易感性以及制定预防肝病和肺病的新策略方面取得了进展。