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Impact of genetic polymorphisms related to innate immune response on respiratory syncytial virus infection in children

Respiratory syncytial virus (RSV) causes lower respiratory tract infections and bronchiolitis, mainly affecting children under 2 years of age and immunocompromised patients. Currently, there are no available vaccines or efficient pharmacological treatments against RSV. In recent years, tremendous ef...

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Autores principales: Córdova-Dávalos, Laura Elena, Hernández-Mercado, Alicia, Barrón-García, Claudia Berenice, Rojas-Martínez, Augusto, Jiménez, Mariela, Salinas, Eva, Cervantes-García, Daniel
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer US 2022
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Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462631/
https://www.ncbi.nlm.nih.gov/pubmed/36085536
http://dx.doi.org/10.1007/s11262-022-01932-6
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author Córdova-Dávalos, Laura Elena
Hernández-Mercado, Alicia
Barrón-García, Claudia Berenice
Rojas-Martínez, Augusto
Jiménez, Mariela
Salinas, Eva
Cervantes-García, Daniel
author_facet Córdova-Dávalos, Laura Elena
Hernández-Mercado, Alicia
Barrón-García, Claudia Berenice
Rojas-Martínez, Augusto
Jiménez, Mariela
Salinas, Eva
Cervantes-García, Daniel
author_sort Córdova-Dávalos, Laura Elena
collection PubMed
description Respiratory syncytial virus (RSV) causes lower respiratory tract infections and bronchiolitis, mainly affecting children under 2 years of age and immunocompromised patients. Currently, there are no available vaccines or efficient pharmacological treatments against RSV. In recent years, tremendous efforts have been directed to understand the pathological mechanisms of the disease and generate a vaccine against RSV. Although RSV is highly infectious, not all the patients who get infected develop bronchiolitis and severe disease. Through various sequencing studies, single nucleotide polymorphisms (SNPs) have been discovered in diverse receptors, cytokines, and transcriptional regulators with crucial role in the activation of the innate immune response, which is implicated in the susceptibility to develop or protect from severe forms of the infection. In this review, we highlighted how variations in the key genes affect the development of innate immune response against RSV. This data would provide crucial information about the mechanisms of viral infection, and in the future, could help in generation of new strategies for vaccine development or generation of the pharmacological treatments.
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spelling pubmed-94626312022-09-10 Impact of genetic polymorphisms related to innate immune response on respiratory syncytial virus infection in children Córdova-Dávalos, Laura Elena Hernández-Mercado, Alicia Barrón-García, Claudia Berenice Rojas-Martínez, Augusto Jiménez, Mariela Salinas, Eva Cervantes-García, Daniel Virus Genes Review Paper Respiratory syncytial virus (RSV) causes lower respiratory tract infections and bronchiolitis, mainly affecting children under 2 years of age and immunocompromised patients. Currently, there are no available vaccines or efficient pharmacological treatments against RSV. In recent years, tremendous efforts have been directed to understand the pathological mechanisms of the disease and generate a vaccine against RSV. Although RSV is highly infectious, not all the patients who get infected develop bronchiolitis and severe disease. Through various sequencing studies, single nucleotide polymorphisms (SNPs) have been discovered in diverse receptors, cytokines, and transcriptional regulators with crucial role in the activation of the innate immune response, which is implicated in the susceptibility to develop or protect from severe forms of the infection. In this review, we highlighted how variations in the key genes affect the development of innate immune response against RSV. This data would provide crucial information about the mechanisms of viral infection, and in the future, could help in generation of new strategies for vaccine development or generation of the pharmacological treatments. Springer US 2022-09-09 2022 /pmc/articles/PMC9462631/ /pubmed/36085536 http://dx.doi.org/10.1007/s11262-022-01932-6 Text en © The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2022, Springer Nature or its licensor holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.
spellingShingle Review Paper
Córdova-Dávalos, Laura Elena
Hernández-Mercado, Alicia
Barrón-García, Claudia Berenice
Rojas-Martínez, Augusto
Jiménez, Mariela
Salinas, Eva
Cervantes-García, Daniel
Impact of genetic polymorphisms related to innate immune response on respiratory syncytial virus infection in children
title Impact of genetic polymorphisms related to innate immune response on respiratory syncytial virus infection in children
title_full Impact of genetic polymorphisms related to innate immune response on respiratory syncytial virus infection in children
title_fullStr Impact of genetic polymorphisms related to innate immune response on respiratory syncytial virus infection in children
title_full_unstemmed Impact of genetic polymorphisms related to innate immune response on respiratory syncytial virus infection in children
title_short Impact of genetic polymorphisms related to innate immune response on respiratory syncytial virus infection in children
title_sort impact of genetic polymorphisms related to innate immune response on respiratory syncytial virus infection in children
topic Review Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9462631/
https://www.ncbi.nlm.nih.gov/pubmed/36085536
http://dx.doi.org/10.1007/s11262-022-01932-6
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