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本文引用的文献

1
Macrophages and cardiac fibroblasts are the main producers of eotaxins and regulate eosinophil trafficking to the heart.巨噬细胞和心脏成纤维细胞是嗜酸性粒细胞趋化因子的主要产生者,并调节嗜酸性粒细胞向心脏的迁移。
Eur J Immunol. 2016 Dec;46(12):2749-2760. doi: 10.1002/eji.201646557. Epub 2016 Oct 25.
2
Current Diagnostic and Therapeutic Aspects of Eosinophilic Myocarditis.嗜酸性粒细胞性心肌炎的当前诊断与治疗方面
Biomed Res Int. 2016;2016:2829583. doi: 10.1155/2016/2829583. Epub 2016 Jan 17.
3
Eosinophilic myocarditis.嗜酸性粒细胞性心肌炎
Herz. 2012 Dec;37(8):849-52. doi: 10.1007/s00059-012-3701-2.
4
Eosinophil development, regulation of eosinophil-specific genes, and role of eosinophils in the pathogenesis of asthma.嗜酸性粒细胞的发育、嗜酸性粒细胞特异性基因的调控以及嗜酸性粒细胞在哮喘发病机制中的作用。
Allergy Asthma Immunol Res. 2012 Mar;4(2):68-79. doi: 10.4168/aair.2012.4.2.68. Epub 2011 Nov 25.
5
Hypereosinophilic syndrome: a multicenter, retrospective analysis of clinical characteristics and response to therapy.嗜酸性粒细胞增多综合征:一项多中心回顾性分析临床特征和治疗反应。
J Allergy Clin Immunol. 2009 Dec;124(6):1319-25.e3. doi: 10.1016/j.jaci.2009.09.022.
6
Treatment of patients with the hypereosinophilic syndrome with mepolizumab.使用美泊利珠单抗治疗高嗜酸性粒细胞综合征患者。
N Engl J Med. 2008 Mar 20;358(12):1215-28. doi: 10.1056/NEJMoa070812. Epub 2008 Mar 16.
7
Rapid progressive eosinophilic cardiomyopathy in a patient with Churg-Strauss syndrome (CSS).一名患有变应性肉芽肿性血管炎(CSS)的患者出现快速进展性嗜酸性粒细胞性心肌病。
Clin Res Cardiol. 2006 May;95(5):289-94. doi: 10.1007/s00392-006-0364-0. Epub 2006 Feb 27.
8
Molecular classification and pathogenesis of eosinophilic disorders: 2005 update.嗜酸性粒细胞增多症的分子分类与发病机制:2005年更新版
Acta Haematol. 2005;114(1):7-25. doi: 10.1159/000085559.
9
Monoclonal anti-interleukin-5 treatment suppresses eosinophil but not T-cell functions.单克隆抗白细胞介素-5治疗可抑制嗜酸性粒细胞功能,但不能抑制T细胞功能。
Eur Respir J. 2003 May;21(5):799-803. doi: 10.1183/09031936.03.00027302.
10
Anti-IL-5 (mepolizumab) therapy induces bone marrow eosinophil maturational arrest and decreases eosinophil progenitors in the bronchial mucosa of atopic asthmatics.抗白细胞介素-5(美泊利单抗)疗法可诱导骨髓嗜酸性粒细胞成熟停滞,并减少特应性哮喘患者支气管黏膜中的嗜酸性粒细胞祖细胞。
J Allergy Clin Immunol. 2003 Apr;111(4):714-9. doi: 10.1067/mai.2003.1382.

抗白细胞介素-5对伴有大量心包积液的嗜酸性粒细胞性心肌炎的治疗作用。

Therapeutic effect of anti-IL-5 on eosinophilic myocarditis with large pericardial effusion.

作者信息

Song Tengyao, Jones David Micheal, Homsi Yamen

机构信息

Center for Molecular and Cellular Physiology, Albany Medical College, Albany, New York, USA.

Department of Pathology, Albany Medical Center, Albany, New York, USA.

出版信息

BMJ Case Rep. 2017 May 24;2017:bcr-2016-218992. doi: 10.1136/bcr-2016-218992.

DOI:10.1136/bcr-2016-218992
PMID:28546236
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5753700/
Abstract

Eosinophilic myocarditis (EM) is a rare myocardial disease that results from various eosinophilic diseases, such as idiopathic hypereosinophilic syndrome, helminth infection, medications and vasculitis. Patients with EM may present with different severities, ranging from mild symptoms to a life-threatening condition. Diagnosis of EM is a challenge and requires an extensive workup, including endomyocardial biopsy. Treatment options are limited because EM is rare and there is a lack of randomised controlled trials. We report a case of EM that presented as cardiac tamponade, which was initially treated with high-dose prednisone and immunosuppressant medications without significant improvement. Mepolizumab (anti-interleukin (IL)-5 antibody) was then applied, leading to an increased ejection fraction and stabilised cardiac function. This case report shows, for the first time, that mepolizumab has novel effects in treating EM. Our findings suggest that mepolizumab can be used as a steroid-sparing agent for treating EM.

摘要

嗜酸性粒细胞性心肌炎(EM)是一种罕见的心肌疾病,由各种嗜酸性粒细胞疾病引起,如特发性高嗜酸性粒细胞综合征、蠕虫感染、药物和血管炎。EM患者可能表现出不同的严重程度,从轻微症状到危及生命的状况。EM的诊断具有挑战性,需要进行全面检查,包括心内膜心肌活检。由于EM罕见且缺乏随机对照试验,治疗选择有限。我们报告一例以心脏压塞为表现的EM病例,最初用大剂量泼尼松和免疫抑制药物治疗,但无明显改善。随后应用美泊利单抗(抗白细胞介素(IL)-5抗体),导致射血分数增加和心功能稳定。本病例报告首次表明美泊利单抗在治疗EM方面具有新的作用。我们的研究结果表明,美泊利单抗可作为治疗EM的类固醇替代药物。