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本文引用的文献

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Benralizumab versus Mepolizumab for Eosinophilic Granulomatosis with Polyangiitis.贝那鲁肽对比美泊利珠单抗用于嗜酸性肉芽肿伴多血管炎。
N Engl J Med. 2024 Mar 7;390(10):911-921. doi: 10.1056/NEJMoa2311155. Epub 2024 Feb 23.
2
Mepolizumab has clinical benefits including oral corticosteroid sparing irrespective of baseline EGPA characteristics.美泊利单抗具有临床益处,包括减少口服糖皮质激素用量,且与基线嗜酸性肉芽肿性多血管炎(EGPA)特征无关。
ERJ Open Res. 2024 Jan 8;10(1). doi: 10.1183/23120541.00509-2023. eCollection 2024 Jan.
3
Eosinophilic granulomatosis with polyangiitis after treatment with dupilumab.使用度普利尤单抗治疗后发生的嗜酸性肉芽肿性多血管炎。
J Allergy Clin Immunol Glob. 2022 Apr 30;1(3):180-182. doi: 10.1016/j.jacig.2022.03.006. eCollection 2022 Aug.
4
Dupilumab for relapsing or refractory sinonasal and/or asthma manifestations in eosinophilic granulomatosis with polyangiitis: a European retrospective study.度普利尤单抗用于治疗嗜酸性肉芽肿性多血管炎的复发性或难治性鼻窦和/或哮喘表现:一项欧洲回顾性研究。
Ann Rheum Dis. 2023 Dec;82(12):1587-1593. doi: 10.1136/ard-2023-224756. Epub 2023 Sep 21.
5
Successful switching from mepolizumab to dupilumab in a patient with EGPA in remission phase and persistent nasal polyposis.一名处于缓解期且患有持续性鼻息肉的嗜酸性肉芽肿性多血管炎(EGPA)患者成功从美泊利单抗转换为度普利尤单抗治疗。
Rheumatology (Oxford). 2024 Mar 1;63(3):e96-e98. doi: 10.1093/rheumatology/kead479.
6
Eosinophilic granulomatosis polyangiitis (EGPA) complicated with periaortitis, precipitating role of dupilumab? A case report a review of the literature.嗜酸性肉芽肿性多血管炎(EGPA)并发大动脉炎,度普利尤单抗的诱发作用?病例报告及文献复习。
RMD Open. 2023 Sep;9(3). doi: 10.1136/rmdopen-2023-003300.
7
Clinical Benefit of Mepolizumab in Eosinophilic Granulomatosis With Polyangiitis for Patients With and Without a Vasculitic Phenotype.美泊利珠单抗治疗伴有或不伴有血管炎表型的嗜酸性肉芽肿性多血管炎患者的临床获益
ACR Open Rheumatol. 2023 Jul;5(7):354-363. doi: 10.1002/acr2.11571. Epub 2023 Jun 13.
8
Eosinophilic granulomatosis with polyangiitis developed after dupilumab administration in patients with eosinophilic chronic rhinosinusitis and asthma: a case report.在患有嗜酸性慢性鼻-鼻窦炎和哮喘的患者中,使用度普利尤单抗治疗后发生嗜酸性肉芽肿伴多血管炎:病例报告。
BMC Pulm Med. 2023 Apr 19;23(1):130. doi: 10.1186/s12890-023-02415-6.
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Mepolizumab therapy improves the most bothersome symptoms in patients with hypereosinophilic syndrome.美泊利珠单抗治疗可改善高嗜酸性粒细胞综合征患者最困扰的症状。
Front Med (Lausanne). 2023 Mar 29;10:1035250. doi: 10.3389/fmed.2023.1035250. eCollection 2023.
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EULAR recommendations for the management of ANCA-associated vasculitis: 2022 update.EULAR 推荐的抗中性粒细胞胞浆抗体相关性血管炎治疗:2022 年更新。
Ann Rheum Dis. 2024 Jan 2;83(1):30-47. doi: 10.1136/ard-2022-223764.

生物制剂在高嗜酸性粒细胞综合征和嗜酸性粒细胞肉芽肿性多血管炎中的应用。

Biologics in Hypereosinophilic Syndrome and Eosinophilic Granulomatosis with Polyangiitis.

机构信息

Human Eosinophil Section, Laboratory of Parasitic Diseases, National Institute of Allergy and Infectious Diseases, National Institutes of Health, Building 4, Room B1-28, 4 Memorial Drive, Bethesda, MD 20892, USA.

National Capital Consortium Allergy & Immunology ellowship, Department of Medicine, Allergy & Immunology Service, Walter Reed National Military Medical Center, Bethesda, MD, USA.

出版信息

Immunol Allergy Clin North Am. 2024 Nov;44(4):629-644. doi: 10.1016/j.iac.2024.07.003. Epub 2024 Aug 16.

DOI:10.1016/j.iac.2024.07.003
PMID:39389714
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11467439/
Abstract

Hypereosinophilic syndrome (HES) and eosinophilic granulomatosis with polyangiitis (EGPA) are complex disorders defined by blood and tissue eosinophilia and heterogeneous clinical manifestations. Historically, the mainstay of therapy for both conditions has been systemic glucocorticoids. However, recent availability of biologics that directly or indirectly target eosinophils has provided new avenues to pursue improved outcomes with decreased toxicity. In this article, we summarize the evidence supporting the use of specific biologics in HES and/or EGPA and provide a framework for their clinical use in patients.

摘要

嗜酸性粒细胞增多综合征(HES)和嗜酸性粒细胞性肉芽肿伴多血管炎(EGPA)是由血液和组织嗜酸性粒细胞增多以及异质性临床表现定义的复杂疾病。历史上,这两种疾病的主要治疗方法都是全身性糖皮质激素。然而,最近可直接或间接靶向嗜酸性粒细胞的生物制剂的出现,为降低毒性的同时改善预后提供了新的途径。本文总结了支持在 HES 和/或 EGPA 中使用特定生物制剂的证据,并为其在患者中的临床应用提供了框架。