• 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

哮喘的抗细胞因子治疗进展。

Update on anticytokine treatment for asthma.

机构信息

Department of Health Science, University Magna Græcia of Catanzaro, Catanzaro, Italy.

出版信息

Biomed Res Int. 2013;2013:104315. doi: 10.1155/2013/104315. Epub 2013 Jun 18.

DOI:10.1155/2013/104315
PMID:23853765
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC3703384/
Abstract

Current advances in the knowledge of asthma pathobiology suggest that anticytokine therapies can be potentially useful for the treatment of this complex and heterogeneous airway disease. Recent evidence is accumulating in support of the efficacy of anti-IL-4, anti-IL-5, and anti-IL-13 drugs. Therefore, these new developments are now changing the global scenario of antiasthma therapies, especially with regard to more severe disease. Current findings referring to variability of individual therapeutic responses highlight that the different asthma subtypes need to be well characterized, in order to implement phenotype-targeted treatments which in the near future will hopefully be mainly based on cytokine-directed biologics.

摘要

目前,哮喘病理生物学知识的进展表明,细胞因子疗法可能对治疗这种复杂和异质性的气道疾病具有潜在的作用。越来越多的证据支持抗 IL-4、抗 IL-5 和抗 IL-13 药物的疗效。因此,这些新的发展正在改变全球的哮喘治疗方案,尤其是在更严重的疾病方面。目前关于个体治疗反应变异性的研究结果表明,不同的哮喘亚型需要进行充分的特征描述,以便实施针对表型的治疗,在不久的将来,希望主要基于细胞因子导向的生物制剂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/362a/3703384/b910f6131b90/BMRI2013-104315.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/362a/3703384/b910f6131b90/BMRI2013-104315.001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/362a/3703384/b910f6131b90/BMRI2013-104315.001.jpg

相似文献

1
Update on anticytokine treatment for asthma.哮喘的抗细胞因子治疗进展。
Biomed Res Int. 2013;2013:104315. doi: 10.1155/2013/104315. Epub 2013 Jun 18.
2
The potential of biologics for the treatment of asthma.生物制剂治疗哮喘的潜力。
Nat Rev Drug Discov. 2012 Dec;11(12):958-72. doi: 10.1038/nrd3792.
3
Biologics in Asthma: Emerging Biologics.哮喘中的生物制剂:新兴的生物制剂。
Immunol Allergy Clin North Am. 2024 Nov;44(4):751-763. doi: 10.1016/j.iac.2024.07.008. Epub 2024 Aug 22.
4
Emerging Biologics in Severe Asthma.重度哮喘中的新兴生物制剂
Immunol Allergy Clin North Am. 2016 Aug;36(3):609-23. doi: 10.1016/j.iac.2016.04.001.
5
Promises and challenges of biologics for severe asthma.生物制剂治疗重度哮喘的前景与挑战。
Biochem Pharmacol. 2020 Sep;179:114012. doi: 10.1016/j.bcp.2020.114012. Epub 2020 May 8.
6
Biologic and New Therapies in Asthma.哮喘的生物制剂及新疗法
Immunol Allergy Clin North Am. 2017 May;37(2):329-343. doi: 10.1016/j.iac.2017.01.007.
7
Personalized medicine with biologics for severe type 2 asthma: current status and future prospects.生物制品个体化医学治疗严重 2 型哮喘:现状与展望。
MAbs. 2018 Jan;10(1):34-45. doi: 10.1080/19420862.2017.1392425. Epub 2017 Nov 14.
8
Biologics or immunotherapeutics for asthma?哮喘的生物制剂或免疫疗法?
Pharmacol Res. 2020 Aug;158:104782. doi: 10.1016/j.phrs.2020.104782. Epub 2020 Apr 8.
9
What has been learned by cytokine targeting of asthma?哮喘的细胞因子靶向治疗有哪些新认识?
J Allergy Clin Immunol. 2022 Aug;150(2):235-249. doi: 10.1016/j.jaci.2022.06.010.
10
Biologics and airway remodeling in severe asthma.生物制剂与重症哮喘中的气道重塑。
Allergy. 2022 Dec;77(12):3538-3552. doi: 10.1111/all.15473. Epub 2022 Aug 23.

引用本文的文献

1
Targeting TSLP in Asthma.靶向哮喘中的胸腺基质淋巴细胞生成素(TSLP)
J Asthma Allergy. 2022 Jun 3;15:749-765. doi: 10.2147/JAA.S275039. eCollection 2022.
2
Effect of Src tyrosine kinase on a rat model of asthma.Src酪氨酸激酶对大鼠哮喘模型的影响。
Exp Ther Med. 2022 Feb;23(2):172. doi: 10.3892/etm.2021.11095. Epub 2021 Dec 27.
3
Targeting Inflammatory Cytokines to Improve Type 2 Diabetes Control.靶向炎症细胞因子以改善 2 型糖尿病控制。

本文引用的文献

1
Dupilumab in persistent asthma with elevated eosinophil levels.度普利尤单抗治疗嗜酸性粒细胞水平升高的持续性哮喘。
N Engl J Med. 2013 Jun 27;368(26):2455-66. doi: 10.1056/NEJMoa1304048. Epub 2013 May 21.
2
Targeting eosinophils in allergy, inflammation and beyond.靶向嗜酸性粒细胞治疗过敏、炎症及其他疾病。
Nat Rev Drug Discov. 2013 Feb;12(2):117-29. doi: 10.1038/nrd3838. Epub 2013 Jan 21.
3
Disabling inflammatory pathways with biologics and resulting clinical outcomes in severe asthma.用生物制剂阻断炎症通路和由此产生的严重哮喘的临床结果。
Biomed Res Int. 2021 Sep 13;2021:7297419. doi: 10.1155/2021/7297419. eCollection 2021.
4
Sevoflurane modulates AQPs (1,5) expression and endoplasmic reticulum stress in mice lung with allergic airway inflammation.七氟醚调控变应性气道炎症小鼠肺水通道蛋白(1,5)表达和内质网应激
Biosci Rep. 2019 Nov 29;39(11). doi: 10.1042/BSR20193282.
5
HSP90 inhibitor geldanamycin reverts IL-13- and IL-17-induced airway goblet cell metaplasia.热休克蛋白 90 抑制剂格尔德霉素逆转白细胞介素-13 和白细胞介素-17 诱导的气道杯状细胞化生。
J Clin Invest. 2019 Feb 1;129(2):744-758. doi: 10.1172/JCI123524. Epub 2019 Jan 14.
6
Potential new targets for drug development in severe asthma.重度哮喘药物研发的潜在新靶点
World Allergy Organ J. 2018 Oct 25;11(1):30. doi: 10.1186/s40413-018-0208-1. eCollection 2018.
7
Benralizumab: From the Basic Mechanism of Action to the Potential Use in the Biological Therapy of Severe Eosinophilic Asthma.贝那鲁肽:从基本作用机制到在严重嗜酸性粒细胞性哮喘的生物治疗中的潜在应用。
Biomed Res Int. 2018 May 10;2018:4839230. doi: 10.1155/2018/4839230. eCollection 2018.
8
Benralizumab in the treatment of severe asthma: design, development and potential place in therapy.倍利珠单抗治疗重度哮喘:设计、研发及在治疗中的潜在地位
Drug Des Devel Ther. 2018 Mar 21;12:619-628. doi: 10.2147/DDDT.S155307. eCollection 2018.
9
Severe eosinophilic asthma: from the pathogenic role of interleukin-5 to the therapeutic action of mepolizumab.重度嗜酸性粒细胞性哮喘:从白细胞介素-5的致病作用到美泊利珠单抗的治疗作用
Drug Des Devel Ther. 2017 Oct 30;11:3137-3144. doi: 10.2147/DDDT.S150656. eCollection 2017.
10
Overlapping Effects of New Monoclonal Antibodies for Severe Asthma.新单克隆抗体治疗严重哮喘的重叠作用。
Drugs. 2017 Oct;77(16):1769-1787. doi: 10.1007/s40265-017-0810-5.
Expert Opin Biol Ther. 2013 Mar;13(3):393-402. doi: 10.1517/14712598.2013.743989. Epub 2013 Jan 7.
4
The potential of biologics for the treatment of asthma.生物制剂治疗哮喘的潜力。
Nat Rev Drug Discov. 2012 Dec;11(12):958-72. doi: 10.1038/nrd3792.
5
Th2 cytokine antagonists: potential treatments for severe asthma.Th2 细胞因子拮抗剂:重度哮喘的潜在治疗方法。
Expert Opin Investig Drugs. 2013 Jan;22(1):49-69. doi: 10.1517/13543784.2013.732997. Epub 2012 Nov 5.
6
The expanding role(s) of eosinophils in health and disease.嗜酸性粒细胞在健康和疾病中的作用不断扩大。
Blood. 2012 Nov 8;120(19):3882-90. doi: 10.1182/blood-2012-06-330845. Epub 2012 Aug 30.
7
Mepolizumab for severe eosinophilic asthma (DREAM): a multicentre, double-blind, placebo-controlled trial.美泊利单抗治疗严重嗜酸性粒细胞性哮喘(DREAM):一项多中心、双盲、安慰剂对照试验。
Lancet. 2012 Aug 18;380(9842):651-9. doi: 10.1016/S0140-6736(12)60988-X.
8
A phase II placebo-controlled study of tralokinumab in moderate-to-severe asthma.一项关于特拉利珠单抗治疗中重度哮喘的 II 期安慰剂对照研究。
Eur Respir J. 2013 Feb;41(2):330-8. doi: 10.1183/09031936.00223411. Epub 2012 Jun 27.
9
IL-4 receptor polymorphisms predict reduction in asthma exacerbations during response to an anti-IL-4 receptor α antagonist.白细胞介素-4 受体多态性可预测抗白细胞介素-4 受体 α 拮抗剂治疗后哮喘恶化的减少。
J Allergy Clin Immunol. 2012 Aug;130(2):516-22.e4. doi: 10.1016/j.jaci.2012.03.030. Epub 2012 Apr 26.
10
Interleukin-33 induces interleukin-17F in bronchial epithelial cells.白细胞介素-33 诱导支气管上皮细胞产生白细胞介素-17F。
Allergy. 2012 Jun;67(6):744-50. doi: 10.1111/j.1398-9995.2012.02825.x. Epub 2012 Apr 28.