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Autoantibodies and autoantigens in autoimmune hepatitis.

机译:自身免疫性肝炎中的自身抗体和自身抗原。

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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.
机译:自身免疫性肝炎(AIH)的诊断取决于排除慢性肝炎或肝损伤的病毒,代谢,遗传和毒性病因。很少有参数可以肯定地预测AIH的存在。自身抗体已在这方面进行了深入评估,并将AIH分为三个血清学亚组:抗核和平滑肌抗体阳性(ANA / SMA,1型),肝肾微粒体抗体阳性(LKM-1,类型) 2),以及可溶性肝抗原/肝胰腺抗原抗体阳性(SLA / LP,3型)AIH。尽管这种分类几乎没有临床意义,但自身抗体谱显示AIH是实体的异质组。 B细胞自身免疫的分子特征已导致鉴定出主要的I期和II期代谢酶以及细胞核的结构和功能成分作为免疫学靶标。对自身抗体及其相应的自身抗原进行了深入研究,为了解疾病的发生,组织特异性和肝自身免疫性疾病的传播提供了线索。

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