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美泊利单抗可减少哮喘患者气道中的嗜酸性粒细胞数量,但不改变其功能表型。

Mepolizumab Attenuates Airway Eosinophil Numbers, but Not Their Functional Phenotype, in Asthma.

作者信息

Kelly Elizabeth A, Esnault Stephane, Liu Lin Ying, Evans Michael D, Johansson Mats W, Mathur Sameer, Mosher Deane F, Denlinger Loren C, Jarjour Nizar N

机构信息

1 Allergy, Pulmonary and Critical Care Medicine Division, Department of Medicine.

2 Department of Biostatistics and Medical Informatics, and.

出版信息

Am J Respir Crit Care Med. 2017 Dec 1;196(11):1385-1395. doi: 10.1164/rccm.201611-2234OC.

Abstract

RATIONALE

Mepolizumab, an IL-5-blocking antibody, reduces exacerbations in patients with severe eosinophilic asthma. Mepolizumab arrests eosinophil maturation; however, the functional phenotype of eosinophils that persist in the blood and airway after administration of IL-5 neutralizing antibodies has not been reported.

OBJECTIVES

To determine the effect of anti-IL-5 antibody on the numbers and phenotypes of allergen-induced circulating and airway eosinophils.

METHODS

Airway inflammation was elicited in participants with mild allergic asthma by segmental allergen challenge before and 1 month after a single intravenous 750-mg dose of mepolizumab. Eosinophils were examined in blood, bronchoalveolar lavage, and endobronchial biopsies 48 hours after challenge.

MEASUREMENTS AND MAIN RESULTS

Segmental challenge without mepolizumab induced a rise in circulating eosinophils, bronchoalveolar lavage eosinophilia, and eosinophil peroxidase deposition in bronchial mucosa. IL-5 neutralization before allergen challenge abolished the allergen-induced rise in circulating eosinophils and expression of IL-3 receptors, whereas airway eosinophilia and eosinophil peroxidase deposition were blunted but not eliminated. Before mepolizumab treatment, bronchoalveolar lavage eosinophils had more surface IL-3 and granulocyte-monocyte colony-stimulating factor receptors, CD69, CD44, and CD23 and decreased IL-5 and eotaxin receptors than blood eosinophils. This activation phenotype indicated by bronchoalveolar lavage eosinophil surface markers, as well as the release of eosinophil peroxidase by eosinophils in the bronchial mucosa, was maintained after mepolizumab.

CONCLUSIONS

Mepolizumab reduced airway eosinophil numbers but had a limited effect on airway eosinophil activation markers, suggesting that these cells retain functionality. This observation may explain why IL-5 neutralization reduces but does not completely eradicate asthma exacerbations. Clinical trial registered with www.clinicaltrials.gov (NCT00802438).

摘要

原理

美泊利单抗是一种抗白细胞介素-5(IL-5)抗体,可减少重度嗜酸性粒细胞性哮喘患者的病情加重。美泊利单抗可阻止嗜酸性粒细胞成熟;然而,在给予IL-5中和抗体后,血液和气道中持续存在的嗜酸性粒细胞的功能表型尚未见报道。

目的

确定抗IL-5抗体对变应原诱导的循环及气道嗜酸性粒细胞数量和表型的影响。

方法

在单次静脉注射750mg美泊利单抗前及注射后1个月,通过节段性变应原激发,使轻度过敏性哮喘参与者诱发气道炎症。激发后48小时,对血液、支气管肺泡灌洗及支气管活检组织中的嗜酸性粒细胞进行检查。

测量指标及主要结果

未使用美泊利单抗的节段性激发可导致循环嗜酸性粒细胞增多、支气管肺泡灌洗嗜酸性粒细胞增多及支气管黏膜嗜酸性粒细胞过氧化物酶沉积增加。变应原激发前进行IL-5中和可消除变应原诱导的循环嗜酸性粒细胞增多及IL-3受体表达,而气道嗜酸性粒细胞增多及嗜酸性粒细胞过氧化物酶沉积虽有所减轻但未消除。在美泊利单抗治疗前,支气管肺泡灌洗嗜酸性粒细胞比血液嗜酸性粒细胞具有更多表面IL-3和粒细胞-单核细胞集落刺激因子受体、CD69、CD44和CD23,而IL-5和嗜酸性粒细胞趋化因子受体减少。支气管肺泡灌洗嗜酸性粒细胞表面标志物所显示的这种活化表型,以及支气管黏膜中嗜酸性粒细胞释放嗜酸性粒细胞过氧化物酶的现象,在美泊利单抗治疗后仍持续存在。

结论

美泊利单抗可减少气道嗜酸性粒细胞数量,但对气道嗜酸性粒细胞活化标志物的影响有限,提示这些细胞仍保留功能。这一观察结果可能解释了为何IL-5中和可减少但不能完全消除哮喘病情加重。临床试验已在www.clinicaltrials.gov注册(NCT00802438)。

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