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自身免疫性肝炎的前沿问题。

Cutting edge issues in autoimmune hepatitis.

机构信息

Institute of Liver Studies, King's College London School of Medicine at King's College Hospital, Denmark Hill, London, SE5 9RS, UK.

出版信息

Clin Rev Allergy Immunol. 2012 Jun;42(3):309-21. doi: 10.1007/s12016-010-8236-9.

Abstract

Autoimmune hepatitis is an inflammatory liver disease affecting mainly females and characterised histologically by interface hepatitis, biochemically by elevated transaminase levels and serologically by circulating autoantibodies and increased levels of immunoglobulin G. Autoimmune hepatitis responds to immunosuppressive treatment, which should be instituted as soon as diagnosis is made. Seropositivity for smooth muscle and/or antinuclear antibody defines type 1 autoimmune hepatitis, while positivity for liver kidney microsomal type 1 antibody defines type 2 autoimmune hepatitis. The aetiology of autoimmune hepatitis is unknown, though both genetic and environmental factors are involved in its expression. The major mechanism of liver damage involves immune reactions against host liver antigens that are not adequately controlled by defective regulatory T cells. Current research aiming at potentiating regulatory T cell function in vitro to reconstitute tolerance in vivo has given promising results.

摘要

自身免疫性肝炎是一种影响主要为女性的炎症性肝病,其组织学特征为界面肝炎,生物化学特征为转氨酶水平升高,血清学特征为循环自身抗体和免疫球蛋白 G 水平升高。自身免疫性肝炎对免疫抑制治疗有反应,应在确诊后尽快开始治疗。平滑肌抗体和/或抗核抗体阳性定义为 1 型自身免疫性肝炎,而肝-肾微粒体抗体 1 阳性定义为 2 型自身免疫性肝炎。自身免疫性肝炎的病因尚不清楚,尽管其表达既涉及遗传因素,也涉及环境因素。肝损伤的主要机制涉及针对宿主肝抗原的免疫反应,而调节性 T 细胞的缺陷不能充分控制这些反应。目前旨在体外增强调节性 T 细胞功能以在体内重建耐受的研究已取得有前景的结果。

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