Evidence map›Paper›PMID 40587183›Full record

ArticleJMIR research protocols2025

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.

Sara Alonso Fernandez, Raquel Reyes-Manzanas, Susana Camara, Juan Mozas-Gutierrez, Myriam Calle-Rubio, Juan Rodriguez-Hermosa, Andres Bodas-Pinedo, Santiago Rueda Esteban, Esther M Lafuente, Jesús Reiné and 1 more

Abstract read
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Article in JMIR research protocols, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Sara Alonso Fernandez *Department of Immunology, Ophthalmology and ORL, Faculty of Medicine, Universidad Complutense de Madrid, Madrid, Spain.ORCID 0009-0007-0018-8997
Raquel Reyes-Manzanas *Department of Immunology, Ophthalmology and ORL, Faculty of Medicine, Universidad Complutense de Madrid, Madrid, Spain.ORCID 0000-0002-5339-8185
Susana CamaraDepartment of Paediatrics, Oxford Vaccine Group, University of Oxford, Oxford, United Kingdom.ORCID 0000-0002-3154-5834
Juan Mozas-GutierrezDepartment of Immunology, Ophthalmology and ORL, Faculty of Medicine, Universidad Complutense de Madrid, Madrid, Spain.ORCID 0009-0004-7267-5581
Myriam Calle-RubioUnit of Pulmonology, Hospital Clínico San Carlos, Madrid, Spain.ORCID 0000-0002-3890-2742
Juan Rodriguez-HermosaUnit of Pulmonology, Hospital Clínico San Carlos, Madrid, Spain.ORCID 0000-0003-0552-2484
Andres Bodas-PinedoDepartment of Medicine, School of Medicine, Universidad Complutense de Madrid, Madrid, Spain.ORCID 0000-0002-0720-8678
Santiago Rueda EstebanPaediatrics Unit, Hospital Clínico San Carlos, Madrid, Spain.ORCID 0000-0001-8630-3210
Esther M LafuenteDepartment of Immunology, Ophthalmology and ORL, Faculty of Medicine, Universidad Complutense de Madrid, Madrid, Spain.ORCID 0000-0001-8466-1022
Jesús Reiné *Department of Immunology, Ophthalmology and ORL, Faculty of Medicine, Universidad Complutense de Madrid, Madrid, Spain.ORCID 0000-0001-7462-2054
Pedro A Reche *Department of Immunology, Ophthalmology and ORL, Faculty of Medicine, Universidad Complutense de Madrid, Madrid, Spain.ORCID 0000-0003-3966-5838

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundHuman 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.

objectiveThis 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.

methodsParticipants 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.

resultsThis 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.

conclusionsHere, 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.

Indexed as

AsthmaObservational Studies as TopicPicornaviridae InfectionsPulmonary Disease, Chronic ObstructiveRhinovirusViral VaccinesAdolescentAdultChildEpitopesFemaleHumansMaleMiddle AgedT-LymphocytesEpitopesViral Vaccinesasthmachronic obstructive pulmonary disease rhinovirusCOPDepitopesexploratoryobservational study.protocolstudy designvaccine

Identifiers

PMID40587183
PMCPMC12260463

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.