Strassburg Christian P, Manns Michael P
Department of Gastroenterology, Hepatology and Endocrinology, Hannover Medical School, Germany.
Semin Liver Dis. 2002 Nov;22(4):339-52. doi: 10.1055/s-2002-35704.
The diagnosis of autoimmune hepatitis (AIH) relies on the exclusion of viral, metabolic, genetic, and toxic etiologies of chronic hepatitis or hepatic injury. There are few parameters that positively predict the presence of AIH. Autoantibodies have been intensively evaluated in this respect and have led to the classification of AIH into three serological subgroups: antinuclear and smooth muscle antibody-positive (ANA/SMA, type 1), liver-kidney microsomal antibody-positive (LKM-1, type 2), and soluble liver antigen/liver-pancreas antigen antibody-positive (SLA/LP, type 3) AIH. Although there are few clinical implications resulting from this classification, autoantibody profiles indicate that AIH is a heterogenous group of entities. The molecular characterization of B cell autoimmunity has led to the identification of major phase I and phase II metabolic enzymes as well as structural and functional components of the cell nucleus as immunologic targets. Autoantibodies and their corresponding autoantigens are intensively studied to provide clues to the understanding of disease initiation, tissue specificity, and propagation of hepatic autoimmune diseases.
自身免疫性肝炎(AIH)的诊断依赖于排除慢性肝炎或肝损伤的病毒、代谢、遗传和毒性病因。几乎没有参数能够明确预测AIH的存在。在这方面,自身抗体已得到深入评估,并由此将AIH分为三个血清学亚组:抗核抗体和平滑肌抗体阳性(ANA/SMA,1型)、肝肾微粒体抗体阳性(LKM-1,2型)以及可溶性肝抗原/肝胰抗原抗体阳性(SLA/LP,3型)AIH。尽管这种分类几乎没有临床意义,但自身抗体谱表明AIH是一组异质性疾病。B细胞自身免疫的分子特征已导致主要的I期和II期代谢酶以及细胞核的结构和功能成分被确定为免疫靶点。对自身抗体及其相应自身抗原进行了深入研究,以提供线索来理解肝脏自身免疫性疾病的发病起始、组织特异性和传播机制。