[Control de asma grave predominantemente eosinofílica con el uso de anti IL-5].

Martha Alicia Ruiz-Peñaloza, José Jesús López-Tiro, Zayra Estefania Ortíz-Monteón, Carolina García-Rosas
{"title":"[Control de asma grave predominantemente eosinofílica con el uso de anti IL-5].","authors":"Martha Alicia Ruiz-Peñaloza, José Jesús López-Tiro, Zayra Estefania Ortíz-Monteón, Carolina García-Rosas","doi":"10.29262/ram.v70i3.1269","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Asthma is a chronic inflammatory disease of the airways, caused by inflammatory cells and mediators, associated with smooth muscle dysfunction, causing variable airflow obstruction. With high, low and mixed type 2 immunoinflammatory mechanisms (endotypes). Severe asthma is that which requires step 4 or 5 of treatment (GINA 2023). The TH2 High phenotype, non-allergic with eosinophilia and FENO, is the second most common. It affects 300 million people around the world.</p><p><strong>Objetive: </strong>Describe asthma biomarkers after the use of antiinterleukin 5, Benralizumab, in adults with severe asthma.</p><p><strong>Methods: </strong>Case report, descriptive study. Patients with severe eosinophilic asthma and chronic polyposis rhinosinusitis under treatment with anti-IL5 were included, evaluating inflammatory biomarkers.</p><p><strong>Results: </strong>Serum eosinophils, FENO, ACT, spirometry, and exacerbations were measured in 8 patients at baseline and 6 months after treatment. The FEV1-FVC was 51% with improvement up to 95% later. 5 patients had FENO > 45 ppm subsequently only 3 continued to be inflamed. Eosinophilia 150 cells and subsequently only 1 patient persisted with eosinophilia 200 cells. Initial ACT < 19 in 7 patients Final ACT >19 in 7 patients. Exacerbations 8 patients with 2 or more exacerba- tions subsequently only 1 patient presented exacerbation.</p><p><strong>Conclusion: </strong>The use of anti-interleukin 5 (benralizumab) does reduce inflammatory markers, improves control and number of exacerbations in the short term. Monoclonal antibodies (Anti IL-5), if they improve inflammatory biomarkers, if clinical characteristics and inflammatory biomarkers are taken into account, it favors adequate asthma control.</p>","PeriodicalId":101421,"journal":{"name":"Revista alergia Mexico (Tecamachalco, Puebla, Mexico : 1993)","volume":"70 4","pages":"199"},"PeriodicalIF":0.0000,"publicationDate":"2023-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Revista alergia Mexico (Tecamachalco, Puebla, Mexico : 1993)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.29262/ram.v70i3.1269","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

Background: Asthma is a chronic inflammatory disease of the airways, caused by inflammatory cells and mediators, associated with smooth muscle dysfunction, causing variable airflow obstruction. With high, low and mixed type 2 immunoinflammatory mechanisms (endotypes). Severe asthma is that which requires step 4 or 5 of treatment (GINA 2023). The TH2 High phenotype, non-allergic with eosinophilia and FENO, is the second most common. It affects 300 million people around the world.

Objetive: Describe asthma biomarkers after the use of antiinterleukin 5, Benralizumab, in adults with severe asthma.

Methods: Case report, descriptive study. Patients with severe eosinophilic asthma and chronic polyposis rhinosinusitis under treatment with anti-IL5 were included, evaluating inflammatory biomarkers.

Results: Serum eosinophils, FENO, ACT, spirometry, and exacerbations were measured in 8 patients at baseline and 6 months after treatment. The FEV1-FVC was 51% with improvement up to 95% later. 5 patients had FENO > 45 ppm subsequently only 3 continued to be inflamed. Eosinophilia 150 cells and subsequently only 1 patient persisted with eosinophilia 200 cells. Initial ACT < 19 in 7 patients Final ACT >19 in 7 patients. Exacerbations 8 patients with 2 or more exacerba- tions subsequently only 1 patient presented exacerbation.

Conclusion: The use of anti-interleukin 5 (benralizumab) does reduce inflammatory markers, improves control and number of exacerbations in the short term. Monoclonal antibodies (Anti IL-5), if they improve inflammatory biomarkers, if clinical characteristics and inflammatory biomarkers are taken into account, it favors adequate asthma control.

查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
[使用抗IL-5控制以嗜酸性粒细胞为主的严重哮喘]。
背景:哮喘是一种由炎症细胞和介质引起的气道慢性炎症性疾病,与平滑肌功能障碍有关,导致可变的气流阻塞。具有高、低和混合的2型免疫炎症机制(内型)。严重哮喘是指需要第4或第5步治疗的哮喘(GINA 2023)。TH2高表型,伴有嗜酸性粒细胞增多和FENO的非过敏性,是第二常见的。它影响着全世界3亿人。目的:描述成人严重哮喘患者使用抗白细胞介素5(Benralizumab)后的哮喘生物标志物。方法:病例报告、描述性研究。纳入接受抗IL5治疗的严重嗜酸性粒细胞性哮喘和慢性息肉病性鼻窦炎患者,评估炎症生物标志物。结果:在基线和治疗后6个月,对8名患者的血清嗜酸性粒细胞、FENO、ACT、肺活量测定和急性加重进行了测量。FEV1-FVC为51%,改善率达95%。5名患者的FENO>45ppm,随后只有3名患者继续发炎。嗜酸性粒细胞增多症150个细胞,随后只有1名患者持续嗜酸性粒增多症200个细胞。7例患者初始ACT<19例,7例患者最终ACT>19例。加重8名患者出现2次或2次以上加重,随后只有1名患者出现加重。结论:在短期内使用抗白细胞介素5(benralizumab)确实可以降低炎症标志物,改善病情控制和恶化次数。单克隆抗体(抗IL-5),如果它们能改善炎症生物标志物,如果考虑到临床特征和炎症生物标志,则有利于充分控制哮喘。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
[Adenovirus-related acute liver failure treated with intravenous immunoglobulin]. [Allergic contact dermatitis due to Furacin®]. [Chronic urticaria as an atypical reaction after a vespid bite]. [Epidemiological profile of allergic respiratory disease in Mexican children]. [Knowledge of mothers of children under 5 years of age about vaccination schedule].
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1