Mepolizumab在嗜酸性肉芽肿合并多血管炎患者中的安全性和有效性。

IF 2 Q3 RESPIRATORY SYSTEM Pulmonary Medicine Pub Date : 2019-03-03 eCollection Date: 2019-01-01 DOI:10.1155/2019/4376380
Ravi Ranjan Pradhan, Gaurav Nepal, Shobha Mandal
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引用次数: 8

摘要

嗜酸性肉芽肿病合并多血管炎(EGPA)是一种罕见的血管炎疾病,累及多器官系统,以哮喘、肺浸润、鼻窦炎、神经病变和周围嗜酸性粒细胞增多为特征。它对心脏、皮肤、肾脏和胃肠道也有影响。白细胞介素-5 (IL-5)参与嗜酸性粒细胞的成熟和激活,其产生在EGPA中增加。EGPA的治疗仅限于全身皮质类固醇和免疫调节剂。这些药物都有明显的副作用。除此之外,患者对这些药物的反应可能令人失望。频繁复发,需要长期中至高剂量糖皮质激素治疗,以及未能达到缓解并不罕见的发现。需要一种能够减少复发频率和全身糖皮质激素剂量并维持持续缓解而无明显副作用的药物。Mepolizumab是IL-5拮抗剂,可能对治疗EGPA患者有价值。因此,我们对mepolizumab在EGPA患者中的疗效和安全性进行了系统评价。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Safety and Efficacy of Mepolizumab in Patients with Eosinophilic Granulomatosis with Polyangiitis.

Eosinophilic granulomatosis with polyangiitis (EGPA) is a rare form of vasculitis disorder which involves multiple organ systems and is characterized by asthma, pulmonary infiltrates, sinusitis, neuropathy, and peripheral eosinophilia. It also has an effect on the heart, skin, kidneys, and gastrointestinal tract. Interlukin-5 (IL-5) is involved in maturation and activation of eosinophil, the production of which is increased in the EGPA. Treatments of EGPA are limited to systemic corticosteroids and immunomodulators. These drugs are associated with significant side effects. Besides this, the response of patients to these drugs may be disappointing. Frequent relapses, the need for long-term medium-to-high-dose glucocorticoid therapy, and failure to achieve remission are not uncommon findings. There is a need for noble agents that could reduce frequent relapses and the dose of systemic glucocorticoids and maintain a sustained remission without significant side effects. Mepolizumab is IL-5 antagonist and may have value in treating patients with EGPA. Therefore, we did a systematic review to evaluate the efficacy and safety of mepolizumab in patients with EGPA.

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来源期刊
Pulmonary Medicine
Pulmonary Medicine RESPIRATORY SYSTEM-
CiteScore
10.20
自引率
0.00%
发文量
4
审稿时长
14 weeks
期刊最新文献
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