• 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

囊性纤维化气道炎症的非侵入性生物标志物

Noninvasive biomarkers of airway inflammation in cystic fibrosis.

作者信息

Sagel Scott D

机构信息

Departmentof Pediatrics, Children's Hospital, University of Colorado Health Sciences Center, Denver, 80218, USA.

出版信息

Curr Opin Pulm Med. 2003 Nov;9(6):516-21. doi: 10.1097/00063198-200311000-00012.

DOI:10.1097/00063198-200311000-00012
PMID:14534405
Abstract

PURPOSE OF REVIEW

Airway inflammation plays a central role in the lung disease of cystic fibrosis (CF). Biomarkers of inflammation may be useful for monitoring disease progression and evaluating response to therapy. Much of our knowledge of the chronic inflammatory process in the CF airway derives from studies of bronchoscopy and bronchoalveolar lavage. A number of noninvasive approaches have been recently developed to more readily assess airway inflammation including sputum induction, collection of exhaled air, analysis of systemic markers of inflammation, and computed tomography imaging.

RECENT FINDINGS

While measurements of biomarkers of inflammation continue to advance our understanding of the underlying disease process, there is as yet no established role for these markers in clinical practice. This review summarizes the current state of knowledge of various inflammatory markers relevant to CF lung disease, with an eye towards application as surrogate outcome measures in CF clinical trials.

SUMMARY

It is hoped that biomarkers obtained by noninvasive means will be useful in determining specific pathways of injury (ie, oxidative or proteolytic) in individual persons with CF and in assessing response to antiinflammatory treatments.

摘要

综述目的

气道炎症在囊性纤维化(CF)肺部疾病中起核心作用。炎症生物标志物可能有助于监测疾病进展并评估治疗反应。我们对CF气道慢性炎症过程的许多了解都来自支气管镜检查和支气管肺泡灌洗研究。最近已开发出多种非侵入性方法来更轻松地评估气道炎症,包括痰液诱导、呼出气收集、炎症系统标志物分析和计算机断层扫描成像。

最新发现

虽然炎症生物标志物的测量继续增进我们对潜在疾病过程的理解,但这些标志物在临床实践中尚未确立明确作用。本综述总结了与CF肺部疾病相关的各种炎症标志物的当前知识状态,着眼于在CF临床试验中作为替代结局指标的应用。

总结

希望通过非侵入性手段获得的生物标志物将有助于确定个体CF患者的特定损伤途径(即氧化或蛋白水解),并评估对抗炎治疗的反应。

相似文献

1
Noninvasive biomarkers of airway inflammation in cystic fibrosis.囊性纤维化气道炎症的非侵入性生物标志物
Curr Opin Pulm Med. 2003 Nov;9(6):516-21. doi: 10.1097/00063198-200311000-00012.
2
Extracellular purines are biomarkers of neutrophilic airway inflammation.细胞外嘌呤是嗜中性气道炎症的生物标志物。
Eur Respir J. 2008 May;31(5):949-56. doi: 10.1183/09031936.00089807. Epub 2008 Feb 6.
3
Sputum biomarkers of inflammation in cystic fibrosis lung disease.囊性纤维化肺病中炎症的痰液生物标志物
Proc Am Thorac Soc. 2007 Aug 1;4(4):406-17. doi: 10.1513/pats.200703-044BR.
4
Airway inflammation in mild cystic fibrosis.轻度囊性纤维化中的气道炎症
J Cyst Fibros. 2017 Jan;16(1):107-115. doi: 10.1016/j.jcf.2016.05.016. Epub 2016 Jun 11.
5
Analysis of inflammatory and immune response biomarkers in sputum and exhaled breath condensate by a multi-parametric biochip array in cystic fibrosis.囊性纤维化患者痰液和呼出气冷凝液中炎症和免疫反应生物标志物的多参数生物芯片阵列分析。
Int J Immunopathol Pharmacol. 2011 Apr-Jun;24(2):423-32. doi: 10.1177/039463201102400215.
6
The CF-Sputum Induction Trial (CF-SpIT) to assess lower airway bacterial sampling in young children with cystic fibrosis: a prospective internally controlled interventional trial.囊性纤维化患儿下呼吸道细菌采样评估的 CF-诱导痰试验(CF-SpIT):一项前瞻性内部对照干预性试验。
Lancet Respir Med. 2018 Jun;6(6):461-471. doi: 10.1016/S2213-2600(18)30171-1. Epub 2018 May 16.
7
Mechanisms and markers of airway inflammation in cystic fibrosis.
Eur Respir J. 2002 Feb;19(2):333-40. doi: 10.1183/09031936.02.00229202.
8
Oxidative stress and abnormal bioactive lipids in early cystic fibrosis lung disease.早期囊性纤维化肺病中的氧化应激和异常生物活性脂质。
J Cyst Fibros. 2019 Nov;18(6):781-789. doi: 10.1016/j.jcf.2019.04.011. Epub 2019 Apr 26.
9
Nebulized hypertonic saline decreases IL-8 in sputum of patients with cystic fibrosis.雾化高渗盐水可降低囊性纤维化患者痰液中的白细胞介素-8。
Am J Respir Crit Care Med. 2011 Jun 1;183(11):1517-23. doi: 10.1164/rccm.201101-0072OC. Epub 2011 Feb 17.
10
Biomarkers of inflammation in infants with cystic fibrosis.婴儿囊性纤维化炎症标志物。
Respir Res. 2018 Jan 8;19(1):6. doi: 10.1186/s12931-017-0713-8.

引用本文的文献

1
Identification of Sputum Biomarkers Predictive of Pulmonary Exacerbations in COPD.识别预测 COPD 肺部恶化的痰液生物标志物。
Chest. 2022 May;161(5):1239-1249. doi: 10.1016/j.chest.2021.10.049. Epub 2021 Nov 18.
2
Biomarkers of inflammation in infants with cystic fibrosis.婴儿囊性纤维化炎症标志物。
Respir Res. 2018 Jan 8;19(1):6. doi: 10.1186/s12931-017-0713-8.
3
An IL-8 Transiently Transgenized Mouse Model for the In Vivo Long-term Monitoring of Inflammatory Responses.一种用于体内长期监测炎症反应的白细胞介素-8瞬时转基因小鼠模型。
J Vis Exp. 2017 Jul 7(125):55499. doi: 10.3791/55499.
4
Mapping targetable inflammation and outcomes with cystic fibrosis biomarkers.利用囊性纤维化生物标志物绘制可靶向的炎症图谱及研究结果
Pediatr Pulmonol. 2017 Nov;52(S48):S21-S28. doi: 10.1002/ppul.23768. Epub 2017 Jul 17.
5
Pro-resolving lipid mediator Resolvin D1 serves as a marker of lung disease in cystic fibrosis.促消退脂质介质解炎素D1作为囊性纤维化肺病的一个标志物。
PLoS One. 2017 Feb 3;12(2):e0171249. doi: 10.1371/journal.pone.0171249. eCollection 2017.
6
Current Concepts and Controversies in Innate Immunity of Cystic Fibrosis Lung Disease.囊性纤维化肺病固有免疫的当前概念与争议
J Innate Immun. 2016;8(6):531-540. doi: 10.1159/000446840. Epub 2016 Jul 1.
7
In vivo imaging of the lung inflammatory response to Pseudomonas aeruginosa and its modulation by azithromycin.铜绿假单胞菌引起的肺部炎症反应的体内成像及其受阿奇霉素的调节作用
J Transl Med. 2015 Aug 4;13:251. doi: 10.1186/s12967-015-0615-9.
8
Metabolomic Evaluation of Neutrophilic Airway Inflammation in Cystic Fibrosis.囊性纤维化中性粒细胞气道炎症的代谢组学评估
Chest. 2015 Aug;148(2):507-515. doi: 10.1378/chest.14-1800.
9
Evaluation of genome-wide expression profiles of blood and sputum neutrophils in cystic fibrosis patients before and after antibiotic therapy.囊性纤维化患者抗生素治疗前后血液和痰液中性粒细胞全基因组表达谱的评估。
PLoS One. 2014 Aug 1;9(8):e104080. doi: 10.1371/journal.pone.0104080. eCollection 2014.
10
Exhaled breath condensate adenosine tracks lung function changes in cystic fibrosis.呼出气冷凝液中的腺苷可追踪囊性纤维化患者的肺功能变化。
Am J Physiol Lung Cell Mol Physiol. 2013 Apr 1;304(7):L504-9. doi: 10.1152/ajplung.00344.2012. Epub 2013 Jan 25.