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Circulating Cytokines and Lymphocyte Subsets in Patients Who Have Recovered from COVID-19
To investigate the immune status of people who previously had COVID-19 infections, we recruited two-week postrecovery patients and analyzed circulating cytokine and lymphocyte subsets. We measured levels of total lymphocytes, CD3(+) T cells, CD4(+) T cells, CD8(+) T cells, CD19(+) B cells, and CD56(...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7695995/ https://www.ncbi.nlm.nih.gov/pubmed/33274223 http://dx.doi.org/10.1155/2020/7570981 |
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author | Hasichaolu, Zhang, Xinri Li, Xin Li, Xin Li, Dongyan |
author_facet | Hasichaolu, Zhang, Xinri Li, Xin Li, Xin Li, Dongyan |
author_sort | Hasichaolu, |
collection | PubMed |
description | To investigate the immune status of people who previously had COVID-19 infections, we recruited two-week postrecovery patients and analyzed circulating cytokine and lymphocyte subsets. We measured levels of total lymphocytes, CD3(+) T cells, CD4(+) T cells, CD8(+) T cells, CD19(+) B cells, and CD56(+) NK cells and the serum concentrations of interleukin- (IL-) 1, IL-4, IL-6, IL-8, IL-10, transforming growth factor beta (TGF-β), tumor necrosis factor alpha (TNF-α), and interferon gamma (IFN-γ) by flow cytometry. We found that in most postrecovery patients, levels of total lymphocytes (66.67%), CD3(+) T cells (54.55%), CD4(+) T cells (54.55%), CD8(+) T cells (81.82%), CD19(+) B cells (69.70%), and CD56(+) NK cells (51.52%) remained lower than normal, whereas most patients showed normal levels of IL-2 (100%), IL-4 (80.88%), IL-6 (79.41%), IL-10 (98.53%), TNF-α (89.71%), IFN-γ (100%), and IL-17 (97.06%). Compared to healthy controls, two-week postrecovery patients had significantly lower absolute numbers of total lymphocytes, CD3(+) T cells, CD4(+) T cells, CD8(+) T cells, CD19(+) B cells, and CD56(+) NK cells, along with significantly higher levels of IL-2, IL-4, IL-6, IL-10, TNF-α, IFN-γ, and IL-17. Among postrecovery patients, T cells, particularly CD4(+) T cells, were positively correlated with CD19(+) B cell counts. Additionally, CD8(+) T cells were positively correlated with CD4(+) T cells and IL-2 levels, and IL-6 positively correlated with TNF-α and IFN-γ. These correlations were not observed in healthy controls. By ROC curve analysis, postrecovery decreases in lymphocyte subsets and increases in cytokines were identified as independent predictors of rehabilitation efficacy. These findings indicate that the immune system gradually recovers following COVID-19 infection; however, the sustained hyperinflammatory response for more than 14 days suggests a need to continue medical observation following discharge from the hospital. Longitudinal studies of a larger cohort of recovered patients are needed to fully understand the consequences of the infection. |
format | Online Article Text |
id | pubmed-7695995 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Hindawi |
record_format | MEDLINE/PubMed |
spelling | pubmed-76959952020-12-02 Circulating Cytokines and Lymphocyte Subsets in Patients Who Have Recovered from COVID-19 Hasichaolu, Zhang, Xinri Li, Xin Li, Xin Li, Dongyan Biomed Res Int Research Article To investigate the immune status of people who previously had COVID-19 infections, we recruited two-week postrecovery patients and analyzed circulating cytokine and lymphocyte subsets. We measured levels of total lymphocytes, CD3(+) T cells, CD4(+) T cells, CD8(+) T cells, CD19(+) B cells, and CD56(+) NK cells and the serum concentrations of interleukin- (IL-) 1, IL-4, IL-6, IL-8, IL-10, transforming growth factor beta (TGF-β), tumor necrosis factor alpha (TNF-α), and interferon gamma (IFN-γ) by flow cytometry. We found that in most postrecovery patients, levels of total lymphocytes (66.67%), CD3(+) T cells (54.55%), CD4(+) T cells (54.55%), CD8(+) T cells (81.82%), CD19(+) B cells (69.70%), and CD56(+) NK cells (51.52%) remained lower than normal, whereas most patients showed normal levels of IL-2 (100%), IL-4 (80.88%), IL-6 (79.41%), IL-10 (98.53%), TNF-α (89.71%), IFN-γ (100%), and IL-17 (97.06%). Compared to healthy controls, two-week postrecovery patients had significantly lower absolute numbers of total lymphocytes, CD3(+) T cells, CD4(+) T cells, CD8(+) T cells, CD19(+) B cells, and CD56(+) NK cells, along with significantly higher levels of IL-2, IL-4, IL-6, IL-10, TNF-α, IFN-γ, and IL-17. Among postrecovery patients, T cells, particularly CD4(+) T cells, were positively correlated with CD19(+) B cell counts. Additionally, CD8(+) T cells were positively correlated with CD4(+) T cells and IL-2 levels, and IL-6 positively correlated with TNF-α and IFN-γ. These correlations were not observed in healthy controls. By ROC curve analysis, postrecovery decreases in lymphocyte subsets and increases in cytokines were identified as independent predictors of rehabilitation efficacy. These findings indicate that the immune system gradually recovers following COVID-19 infection; however, the sustained hyperinflammatory response for more than 14 days suggests a need to continue medical observation following discharge from the hospital. Longitudinal studies of a larger cohort of recovered patients are needed to fully understand the consequences of the infection. Hindawi 2020-11-26 /pmc/articles/PMC7695995/ /pubmed/33274223 http://dx.doi.org/10.1155/2020/7570981 Text en Copyright © 2020 Hasichaolu et al. https://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Article Hasichaolu, Zhang, Xinri Li, Xin Li, Xin Li, Dongyan Circulating Cytokines and Lymphocyte Subsets in Patients Who Have Recovered from COVID-19 |
title | Circulating Cytokines and Lymphocyte Subsets in Patients Who Have Recovered from COVID-19 |
title_full | Circulating Cytokines and Lymphocyte Subsets in Patients Who Have Recovered from COVID-19 |
title_fullStr | Circulating Cytokines and Lymphocyte Subsets in Patients Who Have Recovered from COVID-19 |
title_full_unstemmed | Circulating Cytokines and Lymphocyte Subsets in Patients Who Have Recovered from COVID-19 |
title_short | Circulating Cytokines and Lymphocyte Subsets in Patients Who Have Recovered from COVID-19 |
title_sort | circulating cytokines and lymphocyte subsets in patients who have recovered from covid-19 |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7695995/ https://www.ncbi.nlm.nih.gov/pubmed/33274223 http://dx.doi.org/10.1155/2020/7570981 |
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