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Clinical correlation of influenza and respiratory syncytial virus load measured by digital PCR
Acute respiratory tract infections are a major cause of respiratory morbidity and mortality in pediatric patients worldwide. However, accurate viral and immunologic markers to predict clinical outcomes of this patient population are still lacking. Droplet digital PCR assays for influenza and respira...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720028/ https://www.ncbi.nlm.nih.gov/pubmed/31479459 http://dx.doi.org/10.1371/journal.pone.0220908 |
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author | Hijano, Diego R. Brazelton de Cardenas, Jessica Maron, Gabriela Garner, Cherilyn D. Ferrolino, Jose A. Dallas, Ronald H. Gu, Zhengming Hayden, Randall T. |
author_facet | Hijano, Diego R. Brazelton de Cardenas, Jessica Maron, Gabriela Garner, Cherilyn D. Ferrolino, Jose A. Dallas, Ronald H. Gu, Zhengming Hayden, Randall T. |
author_sort | Hijano, Diego R. |
collection | PubMed |
description | Acute respiratory tract infections are a major cause of respiratory morbidity and mortality in pediatric patients worldwide. However, accurate viral and immunologic markers to predict clinical outcomes of this patient population are still lacking. Droplet digital PCR assays for influenza and respiratory syncytial virus (RSV) were designed and performed in 64 respiratory samples from 23 patients with influenza virus infection and 73 samples from 19 patients with RSV infection. Samples of patients with hematologic malignancies, solid tumors, or sickle cell disease were included. Clinical information from institutional medical records was reviewed to assess disease severity. Samples from patients with fever or respiratory symptoms had a significantly higher viral loads than those from asymptomatic patients. Samples from patients with influenza virus and RSV infection collected at presentation had significantly higher viral loads than those collected from patients after completing a course of oseltamivir or ribavirin, respectively. RSV loads correlated positively with clinical symptoms in patients ≤5 years of age, whereas influenza viral loads were associated with clinical symptoms, irrespective of age. Patients receiving antivirals for influenza and RSV had a significant reduction in viral loads after completing therapy. Digital PCR offers an effective method to monitor the efficacy of antiviral treatment for respiratory tract infections in immunocompromised hosts. |
format | Online Article Text |
id | pubmed-6720028 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-67200282019-09-16 Clinical correlation of influenza and respiratory syncytial virus load measured by digital PCR Hijano, Diego R. Brazelton de Cardenas, Jessica Maron, Gabriela Garner, Cherilyn D. Ferrolino, Jose A. Dallas, Ronald H. Gu, Zhengming Hayden, Randall T. PLoS One Research Article Acute respiratory tract infections are a major cause of respiratory morbidity and mortality in pediatric patients worldwide. However, accurate viral and immunologic markers to predict clinical outcomes of this patient population are still lacking. Droplet digital PCR assays for influenza and respiratory syncytial virus (RSV) were designed and performed in 64 respiratory samples from 23 patients with influenza virus infection and 73 samples from 19 patients with RSV infection. Samples of patients with hematologic malignancies, solid tumors, or sickle cell disease were included. Clinical information from institutional medical records was reviewed to assess disease severity. Samples from patients with fever or respiratory symptoms had a significantly higher viral loads than those from asymptomatic patients. Samples from patients with influenza virus and RSV infection collected at presentation had significantly higher viral loads than those collected from patients after completing a course of oseltamivir or ribavirin, respectively. RSV loads correlated positively with clinical symptoms in patients ≤5 years of age, whereas influenza viral loads were associated with clinical symptoms, irrespective of age. Patients receiving antivirals for influenza and RSV had a significant reduction in viral loads after completing therapy. Digital PCR offers an effective method to monitor the efficacy of antiviral treatment for respiratory tract infections in immunocompromised hosts. Public Library of Science 2019-09-03 /pmc/articles/PMC6720028/ /pubmed/31479459 http://dx.doi.org/10.1371/journal.pone.0220908 Text en © 2019 Hijano et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Article Hijano, Diego R. Brazelton de Cardenas, Jessica Maron, Gabriela Garner, Cherilyn D. Ferrolino, Jose A. Dallas, Ronald H. Gu, Zhengming Hayden, Randall T. Clinical correlation of influenza and respiratory syncytial virus load measured by digital PCR |
title | Clinical correlation of influenza and respiratory syncytial virus load measured by digital PCR |
title_full | Clinical correlation of influenza and respiratory syncytial virus load measured by digital PCR |
title_fullStr | Clinical correlation of influenza and respiratory syncytial virus load measured by digital PCR |
title_full_unstemmed | Clinical correlation of influenza and respiratory syncytial virus load measured by digital PCR |
title_short | Clinical correlation of influenza and respiratory syncytial virus load measured by digital PCR |
title_sort | clinical correlation of influenza and respiratory syncytial virus load measured by digital pcr |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6720028/ https://www.ncbi.nlm.nih.gov/pubmed/31479459 http://dx.doi.org/10.1371/journal.pone.0220908 |
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