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Peripheral blood T cells response in human parainfluenza virus-associated lower respiratory tract infection in children

Human Parainfluenza virus (HPIV) causes lower respiratory tract infections (LRTI) mostly in young children. Respiratory viral infections may decline T cells in circulation and display enhanced pathogenicity. This study is aimed to analyze T cells alterations due to HPIV in children with LRTIs. Child...

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Autores principales: Gul, Aisha, Khan, Sanaullah, Arshad, Muhammad, Anjum, Syed Ishtiaq, Attaullah, Sobia, Ali, Ijaz, Rauf, Abdur, Arshad, Abida, Alghanem, Suliman M., Khan, Shahid Niaz
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499292/
https://www.ncbi.nlm.nih.gov/pubmed/32994745
http://dx.doi.org/10.1016/j.sjbs.2020.07.005
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author Gul, Aisha
Khan, Sanaullah
Arshad, Muhammad
Anjum, Syed Ishtiaq
Attaullah, Sobia
Ali, Ijaz
Rauf, Abdur
Arshad, Abida
Alghanem, Suliman M.
Khan, Shahid Niaz
author_facet Gul, Aisha
Khan, Sanaullah
Arshad, Muhammad
Anjum, Syed Ishtiaq
Attaullah, Sobia
Ali, Ijaz
Rauf, Abdur
Arshad, Abida
Alghanem, Suliman M.
Khan, Shahid Niaz
author_sort Gul, Aisha
collection PubMed
description Human Parainfluenza virus (HPIV) causes lower respiratory tract infections (LRTI) mostly in young children. Respiratory viral infections may decline T cells in circulation and display enhanced pathogenicity. This study is aimed to analyze T cells alterations due to HPIV in children with LRTIs. Children (N = 152) with bronchitis or pneumonia, admitted in tertiary care hospitals were included in the study. Respiratory samples (throat or nasopharyngeal swabs) were taken and HPIV genotypes (1–4) were analyzed through RT-PCR. Peripheral blood T cells, CD3+, CD4+, CD8+, and CD19+, were analyzed in confirmed HPIV positive and healthy control group children through flow cytometry. The positivity rate of HPIV was 24.34% and the most prevalent genotype was HPIV-3 (20.40%). HPIV-1 and HPIV-2 were detected in 0.66% and 02% children respectively. The T lymphocyte counts were observed significantly reduced in children infected with HPIV-3. CD4+ cell (1580 ± 97.87) counts did not change significantly but the lowest CD8+ T cell counts (518.5 ± 74.00) were recorded. Similarly, CD3+ and CD19 cell ratios were also reduced. The CD4/CD8 ratio was significantly higher (3.12 ± 0.59) in the study population as compared to the control group (2.18 ± 0.654). Changes in the count of CD8+ T cells were more pronounced in patients with bronchiolitis and pneumonia. It is concluded that CD8+ T cells show a reduced response to HPIV-3 in children with severe LRTIs suggesting a strong association of these cells with disease severity.
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spelling pubmed-74992922020-09-28 Peripheral blood T cells response in human parainfluenza virus-associated lower respiratory tract infection in children Gul, Aisha Khan, Sanaullah Arshad, Muhammad Anjum, Syed Ishtiaq Attaullah, Sobia Ali, Ijaz Rauf, Abdur Arshad, Abida Alghanem, Suliman M. Khan, Shahid Niaz Saudi J Biol Sci Original Article Human Parainfluenza virus (HPIV) causes lower respiratory tract infections (LRTI) mostly in young children. Respiratory viral infections may decline T cells in circulation and display enhanced pathogenicity. This study is aimed to analyze T cells alterations due to HPIV in children with LRTIs. Children (N = 152) with bronchitis or pneumonia, admitted in tertiary care hospitals were included in the study. Respiratory samples (throat or nasopharyngeal swabs) were taken and HPIV genotypes (1–4) were analyzed through RT-PCR. Peripheral blood T cells, CD3+, CD4+, CD8+, and CD19+, were analyzed in confirmed HPIV positive and healthy control group children through flow cytometry. The positivity rate of HPIV was 24.34% and the most prevalent genotype was HPIV-3 (20.40%). HPIV-1 and HPIV-2 were detected in 0.66% and 02% children respectively. The T lymphocyte counts were observed significantly reduced in children infected with HPIV-3. CD4+ cell (1580 ± 97.87) counts did not change significantly but the lowest CD8+ T cell counts (518.5 ± 74.00) were recorded. Similarly, CD3+ and CD19 cell ratios were also reduced. The CD4/CD8 ratio was significantly higher (3.12 ± 0.59) in the study population as compared to the control group (2.18 ± 0.654). Changes in the count of CD8+ T cells were more pronounced in patients with bronchiolitis and pneumonia. It is concluded that CD8+ T cells show a reduced response to HPIV-3 in children with severe LRTIs suggesting a strong association of these cells with disease severity. Elsevier 2020-10 2020-07-10 /pmc/articles/PMC7499292/ /pubmed/32994745 http://dx.doi.org/10.1016/j.sjbs.2020.07.005 Text en © 2020 The Authors http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Gul, Aisha
Khan, Sanaullah
Arshad, Muhammad
Anjum, Syed Ishtiaq
Attaullah, Sobia
Ali, Ijaz
Rauf, Abdur
Arshad, Abida
Alghanem, Suliman M.
Khan, Shahid Niaz
Peripheral blood T cells response in human parainfluenza virus-associated lower respiratory tract infection in children
title Peripheral blood T cells response in human parainfluenza virus-associated lower respiratory tract infection in children
title_full Peripheral blood T cells response in human parainfluenza virus-associated lower respiratory tract infection in children
title_fullStr Peripheral blood T cells response in human parainfluenza virus-associated lower respiratory tract infection in children
title_full_unstemmed Peripheral blood T cells response in human parainfluenza virus-associated lower respiratory tract infection in children
title_short Peripheral blood T cells response in human parainfluenza virus-associated lower respiratory tract infection in children
title_sort peripheral blood t cells response in human parainfluenza virus-associated lower respiratory tract infection in children
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499292/
https://www.ncbi.nlm.nih.gov/pubmed/32994745
http://dx.doi.org/10.1016/j.sjbs.2020.07.005
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