• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

表型驱动的重症哮喘治疗策略。

Phenotype-Driven Therapeutics in Severe Asthma.

机构信息

Department of Pulmonary, Critical Care, Allergy, and Immunologic Diseases, Wake Forest School of Medicine, Medical Center Blvd, Winston-Salem, NC, 27157, USA.

出版信息

Curr Allergy Asthma Rep. 2017 Feb;17(2):10. doi: 10.1007/s11882-017-0678-1.

DOI:10.1007/s11882-017-0678-1
PMID:28233153
Abstract

Inhaled corticosteroids are the mainstay of asthma treatment using a step-up approach with incremental dosing and additional controller medications in order to achieve symptom control and prevent exacerbations. While most patients respond well to this treatment approach, some patients remain refractory despite high doses of inhaled corticosteroids and a long-acting β-agonist. The problem lies in the heterogeneity of severe asthma, which is further supported by the emergence of severe asthma phenotypes. This heterogeneity contributes to the variability in treatment response. Randomized controlled trials involving add-on therapies in poorly controlled asthma have challenged the idea of a "one size fits all" approach targeting specific phenotypes in their subject selection. This review discusses severe asthma phenotypes from unbiased clustering approaches and the most recent scientific evidence on novel treatments to provide a guide in personalizing severe asthma treatment.

摘要

吸入性皮质类固醇是哮喘治疗的主要方法,采用逐步递增剂量的方法,并使用额外的控制器药物,以实现症状控制和预防恶化。虽然大多数患者对这种治疗方法反应良好,但有些患者尽管使用了高剂量的吸入性皮质类固醇和长效β-激动剂仍无法控制病情。问题在于严重哮喘的异质性,这进一步得到了严重哮喘表型的出现的支持。这种异质性导致了治疗反应的可变性。涉及添加治疗药物的对控制不佳的哮喘的随机对照试验挑战了针对特定表型的“一刀切”方法的理念。这篇综述从无偏聚类方法讨论了严重哮喘表型,并讨论了最新的关于新型治疗方法的科学证据,以在个性化严重哮喘治疗方面提供指导。

相似文献

1
Phenotype-Driven Therapeutics in Severe Asthma.表型驱动的重症哮喘治疗策略。
Curr Allergy Asthma Rep. 2017 Feb;17(2):10. doi: 10.1007/s11882-017-0678-1.
2
Long-acting beta2-agonists versus placebo in addition to inhaled corticosteroids in children and adults with chronic asthma.长效β2受体激动剂与安慰剂用于慢性哮喘儿童和成人并联合吸入性糖皮质激素的比较
Cochrane Database Syst Rev. 2005 Oct 19(4):CD005535. doi: 10.1002/14651858.CD005535.
3
Corticosteroids: still at the frontline in asthma treatment?皮质类固醇:在哮喘治疗中仍处于前沿地位?
Clin Chest Med. 2012 Sep;33(3):531-41. doi: 10.1016/j.ccm.2012.05.004. Epub 2012 Jul 12.
4
Controlling the Risk Domain in Pediatric Asthma through Personalized Care.通过个性化护理控制儿科哮喘的风险领域。
Semin Respir Crit Care Med. 2018 Feb;39(1):36-44. doi: 10.1055/s-0037-1608707. Epub 2018 Feb 10.
5
A randomized, open labeled, comparative study to assess the efficacy and safety of controller medications as add on to inhaled corticosteroid and long-acting β2 agonist in the treatment of moderate-to-severe persistent asthma.一项随机、开放标签、对照研究,旨在评估作为吸入性糖皮质激素和长效β2受体激动剂附加治疗药物的控制药物在治疗中重度持续性哮喘中的疗效和安全性。
J Postgrad Med. 2010 Oct-Dec;56(4):270-4. doi: 10.4103/0022-3859.70937.
6
Long-acting beta-agonist treatment in patients with persistent asthma already receiving inhaled corticosteroids.长效β受体激动剂对已接受吸入性糖皮质激素治疗的持续性哮喘患者的治疗作用
BioDrugs. 2001;15(1):11-24. doi: 10.2165/00063030-200115010-00002.
7
Second-line controller therapy for persistent asthma uncontrolled on inhaled corticosteroids: the step 3 dilemma.吸入性糖皮质激素治疗后仍未控制的持续性哮喘的二线控制疗法:第3步困境。
Drugs. 2002;62(16):2315-32. doi: 10.2165/00003495-200262160-00001.
8
Strategies to prevent exacerbations of childhood asthma.预防儿童哮喘恶化的策略。
Curr Opin Pulm Med. 2019 Jan;25(1):27-33. doi: 10.1097/MCP.0000000000000539.
9
Dual components of optimal asthma therapy: scientific and clinical rationale for the use of long-acting beta-agonists with inhaled corticosteroids.最佳哮喘治疗的双重成分:联合使用长效β受体激动剂与吸入性糖皮质激素的科学及临床依据
J Am Osteopath Assoc. 2001 Sep;101(9):526-33.
10
Benefits of omalizumab as add-on therapy in patients with severe persistent asthma who are inadequately controlled despite best available therapy (GINA 2002 step 4 treatment): INNOVATE.对于重度持续性哮喘患者,尽管接受了最佳可用治疗(《全球哮喘防治创议》2002版第4步治疗)但控制不佳时,奥马珠单抗作为附加治疗的益处:INNOVATE研究。
Allergy. 2005 Mar;60(3):309-16. doi: 10.1111/j.1398-9995.2004.00772.x.

引用本文的文献

1
Targeted Biologic Therapies in Severe Asthma: Mechanisms, Biomarkers, and Clinical Applications.重度哮喘的靶向生物疗法:作用机制、生物标志物及临床应用
Pharmaceuticals (Basel). 2025 Jul 10;18(7):1021. doi: 10.3390/ph18071021.
2
Evidence-Based Approach of Biologic Therapy in Bronchial Asthma.支气管哮喘生物治疗的循证方法
J Clin Med. 2023 Jun 27;12(13):4321. doi: 10.3390/jcm12134321.
3
Critical evaluation of asthma biomarkers in clinical practice.临床实践中哮喘生物标志物的批判性评估。

本文引用的文献

1
Blood eosinophil count and prospective annual asthma disease burden: a UK cohort study.血液嗜酸性粒细胞计数与未来年度哮喘疾病负担:一项英国队列研究。
Lancet Respir Med. 2015 Nov;3(11):849-58. doi: 10.1016/S2213-2600(15)00367-7. Epub 2015 Oct 19.
2
Clinical and inflammatory characteristics of the European U-BIOPRED adult severe asthma cohort.欧洲 U-BIOPRED 成人严重哮喘队列的临床和炎症特征。
Eur Respir J. 2015 Nov;46(5):1308-21. doi: 10.1183/13993003.00779-2015. Epub 2015 Sep 10.
3
Efficacy and safety of tralokinumab in patients with severe uncontrolled asthma: a randomised, double-blind, placebo-controlled, phase 2b trial.
Front Med (Lausanne). 2022 Oct 10;9:969243. doi: 10.3389/fmed.2022.969243. eCollection 2022.
4
Effects of Different Intervention Factors on Vascular Endothelial Growth Factor-Induced Human Airway Smooth Muscle Cell Migration.不同干预因素对血管内皮生长因子诱导的人气道平滑肌细胞迁移的影响。
Can Respir J. 2022 Oct 10;2022:6879539. doi: 10.1155/2022/6879539. eCollection 2022.
5
Human bone marrow-mesenchymal stem cell-derived exosomal microRNA-188 reduces bronchial smooth muscle cell proliferation in asthma through suppressing the JARID2/Wnt/β-catenin axis.人骨髓间充质干细胞来源的外泌体 microRNA-188 通过抑制 JARID2/Wnt/β-连环蛋白轴减少哮喘中的支气管平滑肌细胞增殖。
Cell Cycle. 2022 Feb;21(4):352-367. doi: 10.1080/15384101.2021.2020432. Epub 2022 Jan 2.
6
Classification of Distinct Endotypes in Human Skin Scarring: S.C.A.R.-A Novel Perspective on Dermal Fibrosis.人类皮肤瘢痕的独特表型分类:S.C.A.R.——真皮纤维化的新视角。
Adv Wound Care (New Rochelle). 2022 Mar;11(3):109-120. doi: 10.1089/wound.2020.1364. Epub 2021 Apr 20.
7
miR-135a inhibits airway inflammatory response in asthmatic mice via regulating JAK/STAT signaling pathway.miR-135a 通过调控 JAK/STAT 信号通路抑制哮喘小鼠气道炎症反应。
Braz J Med Biol Res. 2021 Jan 15;54(3):e10023. doi: 10.1590/1414-431X202010023. eCollection 2021.
8
Six gene and TH2 signature expression in endobronchial biopsies of participants with asthma.哮喘患者支气管内膜活检中 6 种基因和 TH2 特征表达。
Immun Inflamm Dis. 2020 Mar;8(1):40-49. doi: 10.1002/iid3.282. Epub 2020 Jan 5.
9
Inhibition of airway remodeling and inflammatory response by Icariin in asthma.淫羊藿苷抑制哮喘气道重塑和炎症反应。
BMC Complement Altern Med. 2019 Nov 19;19(1):316. doi: 10.1186/s12906-019-2743-x.
10
The Effects of Obesity in Asthma.肥胖对哮喘的影响。
Curr Allergy Asthma Rep. 2019 Sep 10;19(10):49. doi: 10.1007/s11882-019-0877-z.
特利鲁单抗治疗重症未控制哮喘患者的疗效和安全性:一项随机、双盲、安慰剂对照、2b 期临床试验。
Lancet Respir Med. 2015 Sep;3(9):692-701. doi: 10.1016/S2213-2600(15)00197-6. Epub 2015 Jul 28.
4
A summary of the new GINA strategy: a roadmap to asthma control.新全球哮喘防治创议(GINA)策略总结:哮喘控制路线图
Eur Respir J. 2015 Sep;46(3):622-39. doi: 10.1183/13993003.00853-2015. Epub 2015 Jul 23.
5
Reslizumab for inadequately controlled asthma with elevated blood eosinophil counts: results from two multicentre, parallel, double-blind, randomised, placebo-controlled, phase 3 trials.瑞利珠单抗治疗血嗜酸性粒细胞计数升高的哮喘控制不佳:两项多中心、平行、双盲、随机、安慰剂对照、3 期临床试验结果。
Lancet Respir Med. 2015 May;3(5):355-66. doi: 10.1016/S2213-2600(15)00042-9. Epub 2015 Feb 23.
6
High blood eosinophil count is a risk factor for future asthma exacerbations in adult persistent asthma.血液嗜酸性粒细胞计数高是成人持续性哮喘未来哮喘加重的一个危险因素。
J Allergy Clin Immunol Pract. 2014 Nov-Dec;2(6):741-50. doi: 10.1016/j.jaip.2014.06.005. Epub 2014 Aug 29.
7
External validation of blood eosinophils, FE(NO) and serum periostin as surrogates for sputum eosinophils in asthma.血液嗜酸性粒细胞、FE(NO)和血清嗜酸性粒细胞阳离子蛋白在外周血替代诱导痰嗜酸性粒细胞在哮喘中的验证。
Thorax. 2015 Feb;70(2):115-20. doi: 10.1136/thoraxjnl-2014-205634. Epub 2014 Nov 24.
8
Identification of asthma phenotypes in a tertiary care medical center.三级医疗中心哮喘表型的识别
Am J Med Sci. 2014 Dec;348(6):480-5. doi: 10.1097/MAJ.0000000000000346.
9
Benralizumab, an anti-interleukin 5 receptor α monoclonal antibody, versus placebo for uncontrolled eosinophilic asthma: a phase 2b randomised dose-ranging study.贝那利珠单抗,一种抗白细胞介素 5 受体 α 单克隆抗体,与安慰剂相比用于治疗未控制的嗜酸性粒细胞性哮喘:一项 2b 期随机剂量范围研究。
Lancet Respir Med. 2014 Nov;2(11):879-890. doi: 10.1016/S2213-2600(14)70201-2. Epub 2014 Oct 8.
10
Oral glucocorticoid-sparing effect of mepolizumab in eosinophilic asthma.美泊利珠单抗在嗜酸性粒细胞性哮喘中的口服糖皮质激素节省作用。
N Engl J Med. 2014 Sep 25;371(13):1189-97. doi: 10.1056/NEJMoa1403291. Epub 2014 Sep 8.