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抗SLA和AMA阳性的乳糜泻:两例报告及自身免疫性肝病血清学评估

Anti-SLA and AMA-positive celiac disease: A report of two cases and evaluation of autoimmune liver serology.

作者信息

Demir Nurhan, Efe Cumali, Olmez Seyhmus, Onur Arzu, Yoshida Eric M

机构信息

Department of Gastroenterology, Diyarbakir Health Science University Training and Research Hospital, Diyarbakir, Turkey.

Department of Gastroenterology, Adana Numune Training and Research Hospital, Adana, Turkey.

出版信息

Hepatol Forum. 2020 May 21;1(2):68-71. doi: 10.14744/hf.2020.2020.0005. eCollection 2020 May.

Abstract

Antibodies to soluble liver antigen (anti-SLA) and anti-mitochondrial autoantibodies (AMA) are two specific serological markers of autoimmune hepatitis (AIH) and primary biliary cholangitis (PBC). They are rarely detected in the sera of patients with non-liver autoimmune disorders. The biochemical, serological, and histological findings of two celiac disease (CD) patients who were seropositive for anti-SLA and/or AMA were evaluated. The data of two female patients who were 28 and 34 years old at the time of CD diagnosis were analyzed. The first patient presented with elevated liver function tests (LFTs) and immunoglobulin (Ig) G values. She was seropositive for both anti-SLA and AMA. A liver biopsy suggested features of AIH but no bile duct injury was noted. In addition to a gluten-free diet (GFD), immunosuppressive therapy was administered to normalize the LFTs. The second patient presented with elevated LFTs, a high IgG level, and a positive anti-SLA finding. A GFD was initiated, which resulted in an excellent clinical and biochemical response. Seropositivity for AMA in the first patient and anti-SLA in the second patient remained unchanged during follow-up but neither patient developed primary biliary cholangitis or AIH. Despite the high specificity of anti-SLA and AMA, these autoantibodies can be detected in CD without having any clinical relevance.

摘要

抗可溶性肝抗原抗体(抗SLA)和抗线粒体自身抗体(AMA)是自身免疫性肝炎(AIH)和原发性胆汁性胆管炎(PBC)的两种特异性血清学标志物。在非肝脏自身免疫性疾病患者的血清中很少检测到它们。对两名抗SLA和/或AMA血清学阳性的乳糜泻(CD)患者的生化、血清学和组织学检查结果进行了评估。分析了两名在CD诊断时年龄分别为28岁和34岁的女性患者的数据。第一名患者肝功能检查(LFTs)和免疫球蛋白(Ig)G值升高。她的抗SLA和AMA均为血清学阳性。肝脏活检提示有AIH特征,但未发现胆管损伤。除了无麸质饮食(GFD)外,还给予了免疫抑制治疗以使LFTs恢复正常。第二名患者表现为LFTs升高、IgG水平高以及抗SLA检测呈阳性。开始采用GFD,结果临床和生化反应良好。在随访期间,第一名患者的AMA血清学阳性和第二名患者的抗SLA血清学阳性均未改变,但两名患者均未发展为原发性胆汁性胆管炎或AIH。尽管抗SLA和AMA具有高度特异性,但这些自身抗体可在CD患者中检测到,且无任何临床相关性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/38a5/9349346/014598742f51/hf-1-068-g001.jpg

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