• 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

针对小儿哮喘和慢性阻塞性肺疾病成人患者的鼻病毒表位组合疫苗免疫反应的体外特征:一项观察性和探索性研究方案

In Vitro Characterization of the Immune Response to an Epitope Ensemble Vaccine Against Rhinovirus in Pediatric Asthma and Adults With Chronic Obstructive Pulmonary Disease: Protocol for an Observational and Exploratory Study.

作者信息

Fernandez Sara Alonso, Reyes-Manzanas Raquel, Camara Susana, Mozas-Gutierrez Juan, Calle-Rubio Myriam, Rodriguez-Hermosa Juan, Bodas-Pinedo Andres, Rueda Esteban Santiago, Lafuente Esther M, Reiné Jesús, Reche Pedro A

机构信息

Department of Immunology, Ophthalmology and ORL, Faculty of Medicine, Universidad Complutense de Madrid, Madrid, Spain.

Department of Paediatrics, Oxford Vaccine Group, University of Oxford, Oxford, United Kingdom.

出版信息

JMIR Res Protoc. 2025 Jun 30;14:e73383. doi: 10.2196/73383.

DOI:10.2196/73383
PMID:40587183
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12260463/
Abstract

BACKGROUND

Human rhinoviruses (HRVs) are the leading cause of upper respiratory tract infections, responsible for over half of all such infections. Infection rates among young children can reach as high as 8-12 episodes per year. While HRV infections typically result in mild common colds, they can also lead to more severe respiratory conditions, often in conjunction with bacterial coinfections. In addition, HRVs are implicated in the exacerbation of obstructive respiratory diseases, including asthma and chronic obstructive pulmonary disease (COPD). T-cell responses play a crucial role in the immune defense against HRV. However, in patients with obstructive respiratory diseases, altered or dysregulated T-cell responses to HRV may not only fail to efficiently eliminate the virus but can also exacerbate inflammation and airway remodeling. Therefore, a deeper understanding of T-cell-mediated responses in the context of HRV infection, especially in vulnerable populations like those with COPD, is critical. It can provide new insights into mechanisms of both protection and disease exacerbation, potentially guiding the development of targeted therapies or vaccines that enhance protective immunity while minimizing harmful inflammation.

OBJECTIVE

This study aims to (1) determine the population-wide coverage of HRV-specific T-cell responses, (2) characterize HRV-specific T-cell recall responses in disease cohorts compared to age-match healthy controls, and (3) identify biomarkers of protection and susceptibility within disease cohorts through a comparative analysis.

METHODS

Participants with asthma and those with COPD, aged 5-15 and 40-70 years, respectively, will be recruited alongside healthy age-matched controls. Peripheral blood samples will be collected following informed consent from adult participants and from parents or guardians of minors, as applicable. Clinical, demographic, immunological, and genetic responses will be assessed both prior to and following in vitro stimulation with a pool of HRV-specific T-cell epitopes. Flow cytometry and functional assays will be used to analyze T-cell responses to HRV epitopes in the context of obstructive respiratory diseases.

RESULTS

This study was funded in January 2023 by the Ministry of Science and Innovation of Spain. The primary aim of the study was achieved within the same year. Recruitment for the secondary and tertiary aims is currently ongoing. Preliminary findings highlight the potential significance of HRV-specific T-cell responses in individuals with asthma and those with COPD. A detailed characterization of these immune responses will provide critical insights into host-pathogen interactions and may serve as a foundation for the development of effective T-cell-based vaccines or immunotherapies targeting HRV.

CONCLUSIONS

Here, we present an ethically approved study protocol for an observational and exploratory study investigating a novel epitope-based vaccine targeting HRV, with a focus on pediatric asthma and adult COPD cohort populations.

INTERNATIONAL REGISTERED REPORT IDENTIFIER (IRRID): DERR1-10.2196/73383.

摘要

背景

人鼻病毒(HRV)是上呼吸道感染的主要病因,占所有此类感染的一半以上。幼儿的感染率每年可达8 - 12次。虽然HRV感染通常导致轻度普通感冒,但它们也可导致更严重的呼吸道疾病,通常与细菌合并感染有关。此外,HRV与阻塞性呼吸道疾病的加重有关,包括哮喘和慢性阻塞性肺疾病(COPD)。T细胞反应在针对HRV的免疫防御中起关键作用。然而,在阻塞性呼吸道疾病患者中,对HRV的T细胞反应改变或失调不仅可能无法有效清除病毒,还可能加剧炎症和气道重塑。因此,深入了解HRV感染情况下T细胞介导的反应,尤其是在像COPD患者这样的易感人群中,至关重要。这可以为保护和疾病加重的机制提供新的见解,有可能指导开发增强保护性免疫同时最小化有害炎症的靶向治疗或疫苗。

目的

本研究旨在(1)确定HRV特异性T细胞反应在全人群中的覆盖范围,(2)与年龄匹配的健康对照相比,描述疾病队列中HRV特异性T细胞回忆反应的特征,以及(3)通过比较分析确定疾病队列中保护和易感性的生物标志物。

方法

将分别招募年龄在5 - 15岁和40 - 70岁的哮喘患者和COPD患者,以及年龄匹配的健康对照。在获得成年参与者以及适用情况下未成年人的父母或监护人的知情同意后,采集外周血样本。在用人鼻病毒特异性T细胞表位池进行体外刺激之前和之后,评估临床、人口统计学、免疫学和基因反应。将使用流式细胞术和功能测定法分析阻塞性呼吸道疾病背景下T细胞对HRV表位的反应。

结果

本研究于2023年1月由西班牙科学与创新部资助。该研究的主要目标在同一年内实现。次要和第三目标的招募工作目前正在进行中。初步研究结果突出了HRV特异性T细胞反应在哮喘患者和COPD患者中的潜在重要性。对这些免疫反应的详细表征将为宿主 - 病原体相互作用提供关键见解,并可能为开发针对HRV的有效T细胞疫苗或免疫疗法奠定基础。

结论

在此,我们展示了一项经伦理批准的观察性和探索性研究方案,该研究调查一种针对HRV的新型表位疫苗,重点关注儿童哮喘和成人COPD队列人群。

国际注册报告识别码(IRRID):DERR1-10.2196/73383

相似文献

1
In Vitro Characterization of the Immune Response to an Epitope Ensemble Vaccine Against Rhinovirus in Pediatric Asthma and Adults With Chronic Obstructive Pulmonary Disease: Protocol for an Observational and Exploratory Study.针对小儿哮喘和慢性阻塞性肺疾病成人患者的鼻病毒表位组合疫苗免疫反应的体外特征:一项观察性和探索性研究方案
JMIR Res Protoc. 2025 Jun 30;14:e73383. doi: 10.2196/73383.
2
Sexual Harassment and Prevention Training性骚扰与预防培训
3
Comparison of the effectiveness of inhaler devices in asthma and chronic obstructive airways disease: a systematic review of the literature.吸入装置在哮喘和慢性阻塞性气道疾病中的有效性比较:文献系统评价
Health Technol Assess. 2001;5(26):1-149. doi: 10.3310/hta5260.
4
Immunostimulants versus placebo for preventing exacerbations in adults with chronic bronchitis or chronic obstructive pulmonary disease.免疫刺激剂与安慰剂在预防慢性支气管炎或慢性阻塞性肺疾病成人恶化中的比较。
Cochrane Database Syst Rev. 2022 Nov 14;11(11):CD013343. doi: 10.1002/14651858.CD013343.pub2.
5
Management of urinary stones by experts in stone disease (ESD 2025).结石病专家对尿路结石的管理(2025年结石病专家共识)
Arch Ital Urol Androl. 2025 Jun 30;97(2):14085. doi: 10.4081/aiua.2025.14085.
6
Sputum colour charts to guide antibiotic self-treatment of acute exacerbation of chronic obstructive pulmonary disease: the Colour-COPD RCT.用于指导慢性阻塞性肺疾病急性加重期抗生素自我治疗的痰液颜色图表:Colour-COPD随机对照试验
Health Technol Assess. 2025 May;29(28):1-42. doi: 10.3310/KPFD5558.
7
Systemic Inflammatory Response Syndrome全身炎症反应综合征
8
Haemophilus influenzae oral vaccination for preventing acute exacerbations of chronic bronchitis and chronic obstructive pulmonary disease.口服流感嗜血杆菌疫苗预防慢性支气管炎和慢性阻塞性肺疾病急性加重
Cochrane Database Syst Rev. 2017 Jun 19;6(6):CD010010. doi: 10.1002/14651858.CD010010.pub3.
9
The Black Book of Psychotropic Dosing and Monitoring.《精神药物剂量与监测黑皮书》
Psychopharmacol Bull. 2024 Jul 8;54(3):8-59.
10
Immunogenicity and seroefficacy of pneumococcal conjugate vaccines: a systematic review and network meta-analysis.肺炎球菌结合疫苗的免疫原性和血清效力:系统评价和网络荟萃分析。
Health Technol Assess. 2024 Jul;28(34):1-109. doi: 10.3310/YWHA3079.

本文引用的文献

1
Designing a multi-epitope vaccine candidate against human rhinovirus C utilizing immunoinformatics approach.利用免疫信息学方法设计针对人鼻病毒C的多表位疫苗候选物。
Front Immunol. 2025 Jan 7;15:1364129. doi: 10.3389/fimmu.2024.1364129. eCollection 2024.
2
Comparison of Rhinovirus A-, B-, and C-Associated Respiratory Tract Illness Severity Based on the 5'-Untranslated Region Among Children Younger Than 5 Years.基于5'非翻译区对5岁以下儿童中与A、B、C型鼻病毒相关的呼吸道疾病严重程度的比较
Open Forum Infect Dis. 2022 Oct 19;9(10):ofac387. doi: 10.1093/ofid/ofac387. eCollection 2022 Oct.
3
Characterization of Conserved and Promiscuous Human Rhinovirus CD4 T Cell Epitopes.
鉴定保守和多功能的人鼻病毒 CD4 T 细胞表位。
Cells. 2021 Sep 2;10(9):2294. doi: 10.3390/cells10092294.
4
Genetic diversity and epidemiology of human rhinovirus among children with severe acute respiratory tract infection in Guangzhou, China.中国广州重症急性呼吸道感染患儿中人类鼻病毒的遗传多样性和流行病学。
Virol J. 2021 Aug 23;18(1):174. doi: 10.1186/s12985-021-01645-6.
5
Human rhinovirus-specific CD8 T cell responses target conserved and unusual epitopes.人鼻病毒特异性 CD8 T 细胞应答针对保守和非保守表位。
FASEB J. 2021 Jan;35(1):e21208. doi: 10.1096/fj.202002165R. Epub 2020 Nov 23.
6
Rhinovirus and Asthma Exacerbations.鼻病毒与哮喘恶化。
Immunol Allergy Clin North Am. 2019 Aug;39(3):335-344. doi: 10.1016/j.iac.2019.03.003. Epub 2019 May 15.
7
Rhinovirus and COPD airway epithelium.鼻病毒与慢性阻塞性肺疾病气道上皮
Pulm Crit Care Med. 2017 Oct;2(3). doi: 10.15761/PCCM.1000139. Epub 2017 Sep 7.
8
The CD8 T Cell Response to Respiratory Virus Infections.CD8 T 细胞对呼吸道病毒感染的免疫反应
Front Immunol. 2018 Apr 9;9:678. doi: 10.3389/fimmu.2018.00678. eCollection 2018.
9
Fundamentals and Methods for T- and B-Cell Epitope Prediction.T 细胞和 B 细胞表位预测的基础与方法。
J Immunol Res. 2017;2017:2680160. doi: 10.1155/2017/2680160. Epub 2017 Dec 28.
10
Rhinovirus Biology, Antigenic Diversity, and Advancements in the Design of a Human Rhinovirus Vaccine.鼻病毒生物学、抗原多样性及人鼻病毒疫苗设计进展
Front Microbiol. 2017 Dec 5;8:2412. doi: 10.3389/fmicb.2017.02412. eCollection 2017.