Thiele Geoffrey M, Freeman Thomas L, Klassen Lynell W
University of Nebraska Medical Center, Department of Internal Medicine, Section of Rheumatology and Immunology, Nebraska Medical Center, Omaha, Nebraska 68198-3205, USA.
Semin Liver Dis. 2004 Aug;24(3):273-87. doi: 10.1055/s-2004-832940.
Clinically, the association of alcoholic liver disease (ALD) with circulating autoantibodies, hypergammaglobulinemia, antibodies to unique hepatic proteins, and cytotoxic lymphocytes reacting against autologous hepatocytes strongly suggests altered immune regulation with an increased activity toward normal self-proteins (loss of tolerance). Experimentally, there are several immune responses generated specifically recognizing self-proteins that are modified by metabolites of alcohol. These data strongly suggest that immune reactions may play a significant role in inducing and sustaining an inflammatory cascade of tissue damage to the liver. Additional support for this comes from the observation that the histological appearance of livers with ALD is that of a chronic active hepatitis-like inflammatory disease. Therefore, the hypothesis that immune mechanisms are involved in recurrent alcoholic hepatitis, although not summarily proven, is reasonable, supported by clinical and experimental evidence, and the subject of this article.
临床上,酒精性肝病(ALD)与循环自身抗体、高球蛋白血症、针对独特肝蛋白的抗体以及针对自体肝细胞的细胞毒性淋巴细胞相关联,这强烈表明免疫调节发生改变,对正常自身蛋白的活性增加(耐受性丧失)。在实验中,有几种免疫反应专门针对被酒精代谢产物修饰的自身蛋白产生。这些数据有力地表明,免疫反应可能在诱导和维持肝脏组织损伤的炎症级联反应中起重要作用。对此的进一步支持来自于观察到ALD患者肝脏的组织学表现为慢性活动性肝炎样炎症性疾病。因此,免疫机制参与复发性酒精性肝炎的假说虽然尚未得到确凿证实,但基于临床和实验证据是合理的,也是本文的主题。