Zhang Lijia, Borish Larry, Smith Anna, Somerville Lindsay, Albon Dana
1University of Virginia School of Medicine, Charlottesville, VA 22908 USA.
2Department of Medicine, University of Virginia School of Medicine, PO Box 800546, Charlottesville, VA 22908 USA.
Allergy Asthma Clin Immunol. 2020 Jan 6;16:3. doi: 10.1186/s13223-019-0397-3. eCollection 2020.
Cystic fibrosis (CF) is characterized by inflammation, progressive lung disease, and respiratory failure. Although the relationship is not well understood, patients with CF are thought to have a higher prevalence of asthma than the general population. CF Foundation (CFF) annual registry data in 2017 reported a prevalence of asthma in CF of 32%. It is difficult to differentiate asthma from CF given similarities in symptoms and reversible obstructive lung function in both diseases. However, a specific asthma phenotype (type 2 inflammatory signature), is often identified in CF patients and this would suggest potential responsiveness to biologics targeting this asthma phenotype. A type 2 inflammatory condition is defined by the presence of an interleukin (IL)-4, IL-5, IL-13 state and is suggested by the presence of an elevated total IgE, specific IgE sensitization, or an elevated absolute eosinophil count (AEC). In this manuscript we report the effects of using mepolizumab in patients with CF and type 2 inflammation.
We present three patients with CF (63, 34 and 24 year of age) and personal history of asthma, who displayed significant eosinophilic inflammation and high total serum IgE concentrations (type 2 inflammation) who were treated with mepolizumab. All three patients were colonized with multiple organisms including and and tested positive for specific IgE to multiple allergens. We examined the effect of mepolizumab on patients' lung function (FEV1), blood markers of type 2 inflammation, systemic corticosteroid use and frequency of CF exacerbations. One patient had a substantial increase in lung function after starting mepolizumab and all three patients had a substantial benefit in regards to reduced oral CCS use. While none of the patients showed significant changes in the exacerbation rates there was markedly reduced requirements for oral CCS with exacerbations. In addition, mepolizumab had a positive effect on type 2 inflammatory markers, reducing markers of allergic inflammation in all 3 patients.
Mepolizumab appears to have a positive effect on clinical course in patients with CF presenting with a type 2 phenotype characterized by allergic sensitization and hyper-eosinophilia.
囊性纤维化(CF)的特征为炎症、进行性肺部疾病和呼吸衰竭。尽管两者关系尚不清楚,但CF患者被认为比普通人群哮喘患病率更高。囊性纤维化基金会(CFF)2017年年度登记数据报告CF患者中哮喘患病率为32%。鉴于两种疾病症状和可逆性阻塞性肺功能相似,很难将哮喘与CF区分开来。然而,CF患者中常可识别出一种特定的哮喘表型(2型炎症特征),这表明针对该哮喘表型的生物制剂可能有效。2型炎症状态由白细胞介素(IL)-4、IL-5、IL-13状态定义,并通过总IgE升高、特异性IgE致敏或绝对嗜酸性粒细胞计数(AEC)升高提示。在本手稿中,我们报告了美泊利珠单抗在CF和2型炎症患者中的应用效果。
我们展示了3例CF患者(年龄分别为63岁、34岁和24岁),有哮喘个人史,表现出显著的嗜酸性粒细胞炎症和高血清总IgE浓度(2型炎症),接受了美泊利珠单抗治疗。所有3例患者均定植有多种微生物,包括[具体微生物名称未给出],并且对多种过敏原的特异性IgE检测呈阳性。我们研究了美泊利珠单抗对患者肺功能(FEV1)、2型炎症血液标志物、全身皮质类固醇使用情况和CF急性加重频率的影响。1例患者开始使用美泊利珠单抗后肺功能大幅改善,所有3例患者在减少口服皮质类固醇使用方面均有显著获益。虽然患者的急性加重率均无显著变化,但急性加重时口服皮质类固醇的需求明显减少。此外,美泊利珠单抗对2型炎症标志物有积极影响,降低了所有3例患者的过敏炎症标志物。
美泊利珠单抗似乎对表现出以过敏致敏和嗜酸性粒细胞增多为特征的2型表型的CF患者的临床病程有积极影响。