Suppr超能文献

巨细胞肝炎伴自身免疫性溶血性贫血:B 细胞耗竭疗法治疗婴儿罕见免疫性疾病的更多证据。

Giant cell hepatitis associated with autoimmune hemolytic anemia: More evidence for B-cell depletion therapy for a rare immune mediated disease of infancy.

机构信息

Hepatology and Liver Transplant Unit IRCCS Ospedale Pediatrico Bambino Gesù, Roma, Italy.

出版信息

Clin Res Hepatol Gastroenterol. 2024 Oct;48(8):102435. doi: 10.1016/j.clinre.2024.102435. Epub 2024 Jul 29.

Abstract

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.

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儿期疾病,其特征为急性肝损伤,组织学上表现为广泛的巨细胞转化和自身免疫性溶血性贫血。GCH-AHA 被认为是免疫介导的疾病,与青少年自身免疫性肝炎是不同的实体疾病。特别是与经典青少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,死亡率更高。事实上,自首次描述以来,泼尼松联合硫唑嘌呤的常规治疗一直被用作一线治疗,但在逐渐减量过程中经常复发,以及由于在早期高剂量长期使用而导致的严重副作用。由于经常复发,已经尝试了几种免疫抑制剂作为二线治疗,但效果并不理想。在肝功能严重受损和/或严重贫血的情况下,静脉注射免疫球蛋白可暂时缓解,但只是暂时缓解。自 2004 年以来,B 细胞耗竭治疗(主要是嵌合抗 CD20 单克隆抗体(利妥昔单抗;RTX))已被用于二线治疗,在难治性病例中取得了令人鼓舞的效果。在本期中,来自中国上海的 20 例 GCH-AHA 患儿的系列报告证实了之前的治疗经验,即在获得完全缓解方面,RTX 或 RTX 治疗方案比常规方案更有效,且安全性良好。迄今为止,对这种罕见疾病的发表经验表明,RTX 应被视为治疗复杂或复发性 GCH-AHA 的基石,并且鉴于其疗效和安全性的证据越来越多,RTX 甚至可以作为一线治疗选择,替代常规治疗,以大大减少累积的类固醇暴露及其副作用。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验