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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.

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

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