• 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

血液类胰蛋白酶和胸腺基质淋巴细胞生成素水平可预测重度哮喘恶化的风险。

Blood tryptase and thymic stromal lymphopoietin levels predict the risk of exacerbation in severe asthma.

机构信息

Department of Chest Medicine, Taipei Veterans General Hospital, No. 201, Sec. 2, Shih-Pai Road, Taipei, 112, Taiwan, ROC.

School of Medicine, National Yang-Ming University, Taipei, Taiwan, ROC.

出版信息

Sci Rep. 2021 Apr 19;11(1):8425. doi: 10.1038/s41598-021-86179-1.

DOI:10.1038/s41598-021-86179-1
PMID:33875671
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8055991/
Abstract

Some patients with severe asthma experience exacerbations despite receiving multiple therapy. The risk of exacerbation and heterogeneous response to treatment may be associated with specific inflammatory molecules that are responsive or resistant to corticosteroids. We aimed to identify the independent factors predictive for the future risk of exacerbation in patients with severe asthma. In this multi-center prospective observational study, 132 patients with severe asthma were enrolled and divided into exacerbation (n = 52) and non-exacerbation (n = 80) groups on the basis of exacerbation rate after a 1-year follow-up period. We found that previous history of severe-to-serious exacerbation, baseline blood eosinophil counts (≥ 291cells/μL), and serum tryptase (≤ 1448 pg/mL) and thrymic stromal lymphopoietin (TSLP) levels (≥ 25 pg/mL) independently predicted the future development of exacerbation with adjusted odds ratios (AOR) of 3.27, 6.04, 2.53 and 8.67, respectively. Notably, the patients with high blood eosinophil counts and low tryptase levels were likely to have more exacerbations than those with low blood eosinophil counts and high tryptase levels (AOR 16.9). TSLP potentially played the pathogenic role across different asthma phenotypes. TSLP and tryptase levels may be implicated in steroid resistance and responsiveness in the asthma inflammatory process. High blood eosinophil counts and low serum tryptase levels predict a high probability of future asthma exacerbation.

摘要

一些严重哮喘患者尽管接受了多种治疗仍会出现恶化。恶化的风险和对治疗的异质性反应可能与对皮质类固醇有反应或耐药的特定炎症分子有关。我们旨在确定严重哮喘患者未来恶化风险的独立预测因素。在这项多中心前瞻性观察研究中,我们招募了 132 名严重哮喘患者,并根据 1 年随访期间的恶化率将其分为恶化组(n=52)和非恶化组(n=80)。我们发现,既往严重至严重恶化史、基线血嗜酸性粒细胞计数(≥291 个细胞/μL)以及血清胰蛋白酶(≤1448 pg/mL)和胸腺基质淋巴细胞生成素(TSLP)水平(≥25 pg/mL)可独立预测未来恶化的发展,调整后的优势比(AOR)分别为 3.27、6.04、2.53 和 8.67。值得注意的是,高血嗜酸性粒细胞计数和低胰蛋白酶水平的患者比低血嗜酸性粒细胞计数和高胰蛋白酶水平的患者更容易出现更多的恶化(AOR 16.9)。TSLP 可能在不同的哮喘表型中发挥致病作用。TSLP 和胰蛋白酶水平可能与哮喘炎症过程中的类固醇耐药性和反应性有关。高血嗜酸性粒细胞计数和低血清胰蛋白酶水平预示着未来发生哮喘恶化的可能性较大。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fe7/8055991/45de7d4c8596/41598_2021_86179_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fe7/8055991/0e843bdc0f56/41598_2021_86179_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fe7/8055991/45de7d4c8596/41598_2021_86179_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fe7/8055991/0e843bdc0f56/41598_2021_86179_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/8fe7/8055991/45de7d4c8596/41598_2021_86179_Fig2_HTML.jpg

相似文献

1
Blood tryptase and thymic stromal lymphopoietin levels predict the risk of exacerbation in severe asthma.血液类胰蛋白酶和胸腺基质淋巴细胞生成素水平可预测重度哮喘恶化的风险。
Sci Rep. 2021 Apr 19;11(1):8425. doi: 10.1038/s41598-021-86179-1.
2
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.
3
Ability of Serum IgE Concentration to Predict Exacerbation Risk and Benralizumab Efficacy for Patients with Severe Eosinophilic Asthma.血清 IgE 浓度预测重度嗜酸性粒细胞性哮喘患者恶化风险和 benralizumab 疗效的能力。
Adv Ther. 2020 Feb;37(2):718-729. doi: 10.1007/s12325-019-01191-2. Epub 2019 Dec 14.
4
Severe asthma exacerbations in the United States:: Incidence, characteristics, predictors, and effects of biologic treatments.美国严重哮喘恶化情况:发生率、特征、预测因素和生物治疗的效果。
Ann Allergy Asthma Immunol. 2021 Nov;127(5):579-587.e1. doi: 10.1016/j.anai.2021.07.010. Epub 2021 Jul 15.
5
Sputum Type 2 Markers Could Predict Remission in Severe Asthma Treated With Anti-IL-5.抗白细胞介素-5 治疗重度哮喘时,痰 2 型标志物可预测缓解
Chest. 2023 Jun;163(6):1368-1379. doi: 10.1016/j.chest.2023.01.037. Epub 2023 Feb 3.
6
The association between blood eosinophil count and benralizumab efficacy for patients with severe, uncontrolled asthma: subanalyses of the Phase III SIROCCO and CALIMA studies.严重未控制哮喘患者血液嗜酸性粒细胞计数与贝那利珠单抗疗效之间的关联:III期SIROCCO和CALIMA研究的亚组分析
Curr Med Res Opin. 2017 Sep;33(9):1605-1613. doi: 10.1080/03007995.2017.1347091. Epub 2017 Jul 19.
7
Exacerbation Profile and Risk Factors in a Type-2-Low Enriched Severe Asthma Cohort: A Clinical Trial to Assess Asthma Exacerbation Phenotypes.2 低水平富集严重哮喘队列的加重特征和危险因素:评估哮喘加重表型的临床试验。
Am J Respir Crit Care Med. 2022 Sep 1;206(5):545-553. doi: 10.1164/rccm.202201-0129OC.
8
Association between Serum Levels of Interleukin-25/Thymic Stromal Lymphopoietin and the Risk of Exacerbation of Chronic Obstructive Pulmonary Disease.白细胞介素-25/胸腺基质淋巴细胞生成素与慢性阻塞性肺疾病加重风险的关系。
Biomolecules. 2023 Mar 20;13(3):564. doi: 10.3390/biom13030564.
9
Elevated serum OX40L is a biomarker for identifying corticosteroid resistance in pediatric asthmatic patients.血清 OX40L 水平升高可作为识别儿童哮喘患者糖皮质激素抵抗的生物标志物。
BMC Pulm Med. 2019 Mar 19;19(1):66. doi: 10.1186/s12890-019-0819-5.
10
Severe eosinophilic asthma treated with mepolizumab stratified by baseline eosinophil thresholds: a secondary analysis of the DREAM and MENSA studies.美泊利珠单抗治疗嗜酸粒细胞性哮喘的疗效分层:基于基线嗜酸粒细胞阈值的 DREAM 和 MENSA 研究的二次分析。
Lancet Respir Med. 2016 Jul;4(7):549-556. doi: 10.1016/S2213-2600(16)30031-5. Epub 2016 May 10.

引用本文的文献

1
Thymic stromal lymphopoietin in leukemia: A double-edged sword?白血病中的胸腺基质淋巴细胞生成素:一把双刃剑?
Leuk Res Rep. 2025 Jul 23;24:100530. doi: 10.1016/j.lrr.2025.100530. eCollection 2025.
2
Increased eosinophils after oral corticosteroid treatment for asthma exacerbation correlated with longer ER stays and persisting thymic stromal lymphopoietin and increased Park2.口服皮质类固醇治疗哮喘急性加重后嗜酸性粒细胞增多与急诊室停留时间延长、胸腺基质淋巴细胞生成素持续存在及Park2增加相关。
Sci Rep. 2025 Jul 3;15(1):23755. doi: 10.1038/s41598-025-07102-6.
3
Baseline type 2 biomarker levels and clinical remission predictors in children with asthma.

本文引用的文献

1
Investigation of the relationship between IL-6 and type 2 biomarkers in patients with severe asthma.探讨严重哮喘患者中白细胞介素 6(IL-6)与 2 型生物标志物之间的关系。
J Allergy Clin Immunol. 2020 Jan;145(1):430-433. doi: 10.1016/j.jaci.2019.08.031. Epub 2019 Sep 9.
2
The emerging role of mast cell proteases in asthma.肥大细胞蛋白酶在哮喘中的新作用。
Eur Respir J. 2019 Oct 31;54(4). doi: 10.1183/13993003.00685-2019. Print 2019 Oct.
3
Diagnosis of severe asthma.严重哮喘的诊断。
哮喘患儿的基线2型生物标志物水平及临床缓解预测因素
Front Immunol. 2025 May 28;16:1492644. doi: 10.3389/fimmu.2025.1492644. eCollection 2025.
4
Innate Immunity and Asthma Exacerbations: Insights From Human Models.先天性免疫与哮喘急性发作:来自人体模型的见解
Immunol Rev. 2025 Mar;330(1):e70016. doi: 10.1111/imr.70016.
5
Vascular remodeling and TSLP/angiogenin overexpression in severe mixed asthma.重度混合性哮喘中的血管重塑及TSLP/血管生成素过表达
Respir Res. 2025 Feb 28;26(1):78. doi: 10.1186/s12931-025-03133-9.
6
and Expression Levels in Peripheral Blood as Potential Biomarkers in Patients with Chronic Rhinosinusitis with Nasal Polyps.以及外周血中的表达水平作为鼻息肉慢性鼻窦炎患者的潜在生物标志物。
Int J Mol Sci. 2025 Jan 30;26(3):1227. doi: 10.3390/ijms26031227.
7
Differences in the direct effects of various type 2 cytokines on functions of blood eosinophils from healthy subjects.各种2型细胞因子对健康受试者血液嗜酸性粒细胞功能的直接影响的差异。
Asia Pac Allergy. 2024 Dec;14(4):183-190. doi: 10.5415/apallergy.0000000000000157. Epub 2024 Aug 16.
8
House dust mites stimulate thymic stromal lymphopoietin production in human bronchial epithelial cells and promote airway remodeling through activation of PAR2 and ERK signaling pathway.屋尘螨通过激活 PAR2 和 ERK 信号通路刺激人支气管上皮细胞产生胸腺基质淋巴细胞生成素,并促进气道重塑。
Sci Rep. 2024 Nov 19;14(1):28649. doi: 10.1038/s41598-024-79226-0.
9
Regulation of Airway Epithelial-Derived Alarmins in Asthma: Perspectives for Therapeutic Targets.哮喘中气道上皮源性警报素的调控:治疗靶点展望
Biomedicines. 2024 Oct 11;12(10):2312. doi: 10.3390/biomedicines12102312.
10
Higher levels of basal serum tryptase are associated with sensitization, FeNO, allergic morbidity, and lower control of allergic asthma in teenagers from the PARIS birth cohort.在巴黎出生队列研究中的青少年中,基础血清类胰蛋白酶水平较高与致敏、呼出气一氧化氮(FeNO)、变应性疾病以及过敏性哮喘控制不佳相关。
Allergy. 2025 Feb;80(2):584-587. doi: 10.1111/all.16284. Epub 2024 Aug 19.
Med J Aust. 2018 Jul 16;209(S2):S3-S10. doi: 10.5694/mja18.00125.
4
TSLP promotes asthmatic airway remodeling via p38-STAT3 signaling pathway in human lung fibroblast.胸腺基质淋巴细胞生成素通过人肺成纤维细胞中的p38-信号转导子和转录激活子3信号通路促进哮喘气道重塑。
Exp Lung Res. 2018 Aug;44(6):288-301. doi: 10.1080/01902148.2018.1536175. Epub 2018 Nov 14.
5
Thymic Stromal Lymphopoietin Isoforms, Inflammatory Disorders, and Cancer.胸腺基质淋巴细胞生成素亚型、炎症性疾病与癌症
Front Immunol. 2018 Jul 13;9:1595. doi: 10.3389/fimmu.2018.01595. eCollection 2018.
6
Targeting cytokines to treat asthma and chronic obstructive pulmonary disease.针对细胞因子治疗哮喘和慢性阻塞性肺疾病。
Nat Rev Immunol. 2018 Jul;18(7):454-466. doi: 10.1038/s41577-018-0006-6.
7
Elevated Expression of IL-33 and TSLP in the Airways of Human Asthmatics In Vivo: A Potential Biomarker of Severe Refractory Disease.哮喘患者气道中 IL-33 和 TSLP 的表达升高:一种潜在的严重难治性疾病的生物标志物。
J Immunol. 2018 Apr 1;200(7):2253-2262. doi: 10.4049/jimmunol.1701455. Epub 2018 Feb 16.
8
Pathological Roles of Neutrophil-Mediated Inflammation in Asthma and Its Potential for Therapy as a Target.中性粒细胞介导致炎在哮喘中的病理作用及其作为治疗靶点的潜力。
J Immunol Res. 2017;2017:3743048. doi: 10.1155/2017/3743048. Epub 2017 Nov 22.
9
After asthma: redefining airways diseases.哮喘之后:重新定义气道疾病。
Lancet. 2018 Jan 27;391(10118):350-400. doi: 10.1016/S0140-6736(17)30879-6. Epub 2017 Sep 11.
10
Eosinophilic and Noneosinophilic Asthma.嗜酸性粒细胞性和非嗜酸性粒细胞性哮喘
Am J Respir Crit Care Med. 2018 Jan 1;197(1):22-37. doi: 10.1164/rccm.201611-2232PP.