伴有自身免疫性溶血性贫血的巨细胞性肝炎:B 细胞耗竭疗法治疗婴儿期罕见免疫介导疾病的更多证据。

IF 2.6 4区 医学 Q2 GASTROENTEROLOGY & HEPATOLOGY
Giuseppe Maggiore, Marco Sciveres
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引用次数: 0

摘要

巨细胞肝炎伴自身免疫性溶血性贫血(GCH-AHA)是一种罕见但严重的婴幼儿疾病,表现为急性肝损伤,组织学特征为广泛的巨细胞转化和自身免疫性溶血。GCH-AHA 被认为是由免疫介导的,但与幼年自身免疫性肝炎不同。特别是,与传统的幼年自身免疫性肝炎相比,GCH-AHA 对常规免疫抑制治疗的反应较差,死亡风险较高。事实上,自 GCH-AHA 首次被描述以来,泼尼松联合硫唑嘌呤的常规疗法一直被用作一线治疗,但在逐渐减量的过程中会频繁复发,而且在幼年时期长期大剂量使用会产生严重的副作用。由于经常复发,人们尝试了多种免疫抑制剂作为二线疗法,但效果不佳。在严重肝功能障碍和/或严重贫血的情况下,通过静脉注射免疫球蛋白可获得暂时缓解,但只是暂时性反应。自2004年起,人们开始使用B细胞清除疗法,主要是嵌合抗CD20单克隆抗体(利妥昔单抗;RTX),这种疗法主要用于难治性病例的二线治疗,效果令人鼓舞。本期报告了来自中国上海的20例GCH-AHA患儿,证实了以往的治疗经验,即与传统治疗方案相比,RTX或RTX治疗方案在获得完全缓解方面疗效更佳,且安全性良好。迄今为止,已发表的有关这种罕见疾病的经验表明,RTX 应被视为 GCH-AHA 复杂病例或复发病例的治疗基石,而且鉴于其疗效和安全性方面的证据越来越多,RTX 甚至可以作为常规治疗之外的一线疗法,以大幅减少类固醇的累积暴露及其副作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Giant cell hepatitis associated with autoimmune hemolytic anemia: More evidence for B-cell depletion therapy for a rare immune mediated disease of infancy

Giant cell hepatitis associated with autoimmune hemolytic anemia (GCH-AHA) is a rare but severe disease of infancy defined by an acute liver injury, histologically characterized by a widespread giant cell transformation and by an autoimmune hemolysis. GCH-AHA is thought to be immune-mediated being however a distinct entity from juvenile autoimmune hepatitis. In particular, GCH-AHA displays a less favorable response to conventional immunosuppressive treatment compared to classical juvenile autoimmune hepatitis, carrying a higher risk of mortality. In fact, since his first description, conventional therapy with prednisone with azathioprine has been used as first line treatment, however with frequent relapses during tapering, as well as severe side effects related to its prolonged use at high doses in early age. Due to the frequent occurrence of relapse, several immunosuppressive drugs have been tried as second line therapy with doubtful success. In case of severe liver dysfunction and/or severe anemia, transitory remission has been achieved with intravenous immunoglobulins administration, however with temporary response. B-cell depletion treatment, mostly with chimeric anti-CD20 monoclonal antibody (rituximab; RTX) has been used since 2004 with encouraging results mostly in refractory cases as second-line therapy. In this issue, the report of a series of 20 children with GCH-AHA from Shanghai, China, confirms the previous treatment experiences of a greater efficacy in obtaining complete remission of RTX or RTX treatment regimens compared to conventional regimens, with a good safety. To date, published experience with this rare disease suggests that RTX should be considered the cornerstone of treatment for complicated or relapsing cases of GCH-AHA and given the increasing evidence on its efficacy and safety, RTX might be even an acceptable option as first line therapy beside conventional treatment, to drastically reduce the cumulative steroids exposure and its side effects.

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来源期刊
CiteScore
4.30
自引率
3.70%
发文量
198
审稿时长
42 days
期刊介绍: Clinics and Research in Hepatology and Gastroenterology publishes high-quality original research papers in the field of hepatology and gastroenterology. The editors put the accent on rapid communication of new research and clinical developments and so called "hot topic" issues. Following a clear Editorial line, besides original articles and case reports, each issue features editorials, commentaries and reviews. The journal encourages research and discussion between all those involved in the specialty on an international level. All articles are peer reviewed by international experts, the articles in press are online and indexed in the international databases (Current Contents, Pubmed, Scopus, Science Direct). Clinics and Research in Hepatology and Gastroenterology is a subscription journal (with optional open access), which allows you to publish your research without any cost to you (unless you proactively chose the open access option). Your article will be available to all researchers around the globe whose institution has a subscription to the journal.
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