Suppr超能文献

利妥昔单抗治疗儿童难治性自身免疫性溶血性贫血

Rituximab for refractory childhood autoimmune hemolytic anemia.

作者信息

Motto David G, Williams James A, Boxer Laurence A

机构信息

Department of Pediatric Hematology/Oncology, University of Michigan, Ann Arbor, MI, USA.

出版信息

Isr Med Assoc J. 2002 Nov;4(11):1006-8.

Abstract

BACKGROUND

Chronic childhood autoimmune hemolytic anemia is an uncommon disorder that is associated with significant morbidity. Treatment with high dose steroids, splenectomy and frequent blood transfusions results in a myriad of complications including growth failure, bone demineralization, Cushing's syndrome, immunosuppression, and transfusional hemosiderosis.

OBJECTIVES

To investigate the efficacy of the monoclonal anti-CD20 antibody, rituximab, in treating children with AIHA.

METHODS

Four children with chronic AIHA, including two with prior splenectomy, who were dependent on high dose steroids and refractory to other immunosuppressive regimens were treated with four to six weekly doses of rituximab at a dose of 375 mg/m2.

RESULTS

All four patients became transfusion-independent and were taken off prednisone completely. Adverse effects included infusion-related reactions that were mild, and infectious complications of Pneumocystis carinii pneumonia and varicella pneumonia.

CONCLUSIONS

Treatment with rituximab appears promising for refractory AIHA; if may obviate the need for prednisone and may result in sustained disease remissions in some patients.

摘要

背景

儿童慢性自身免疫性溶血性贫血是一种罕见疾病,伴有严重的发病率。高剂量类固醇、脾切除术和频繁输血治疗会导致多种并发症,包括生长发育迟缓、骨质脱矿、库欣综合征、免疫抑制和输血性含铁血黄素沉着症。

目的

研究单克隆抗CD20抗体利妥昔单抗治疗自身免疫性溶血性贫血(AIHA)患儿的疗效。

方法

4例慢性AIHA患儿,其中2例曾行脾切除术,依赖高剂量类固醇且对其他免疫抑制方案无效,接受每周4至6次剂量为375mg/m²的利妥昔单抗治疗。

结果

所有4例患者均不再依赖输血,且完全停用泼尼松。不良反应包括轻度的输液相关反应,以及卡氏肺孢子虫肺炎和水痘肺炎等感染并发症。

结论

利妥昔单抗治疗难治性AIHA似乎很有前景;它可能无需使用泼尼松,并可能使一些患者的疾病得到持续缓解。

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