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Long-term infection of SARS-CoV-2 changed the body's immune status
The outbreak of SARS-CoV-2-associated pneumonia, a disease called COVID-19, has caused a pandemic worldwide. To investigate the immune responses after infection of SARS-CoV-2 in non-critical patients may help to better understand the disease progression. We collected 334 confirmed COVID-19 cases inc...
Autores principales: | , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Published by Elsevier Inc.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351676/ https://www.ncbi.nlm.nih.gov/pubmed/32659373 http://dx.doi.org/10.1016/j.clim.2020.108524 |
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author | Lin, Lan Luo, Shanshan Qin, Renjie Yang, Mengling Wang, Xiaobei Yang, Qianqian Zhang, Yang Wang, Quansheng Zhu, Rui Fan, Heng Wang, Haijun Hu, Yu Wang, Lin Hu, Desheng |
author_facet | Lin, Lan Luo, Shanshan Qin, Renjie Yang, Mengling Wang, Xiaobei Yang, Qianqian Zhang, Yang Wang, Quansheng Zhu, Rui Fan, Heng Wang, Haijun Hu, Yu Wang, Lin Hu, Desheng |
author_sort | Lin, Lan |
collection | PubMed |
description | The outbreak of SARS-CoV-2-associated pneumonia, a disease called COVID-19, has caused a pandemic worldwide. To investigate the immune responses after infection of SARS-CoV-2 in non-critical patients may help to better understand the disease progression. We collected 334 confirmed COVID-19 cases including 212 still in hospital with nucleic acid test positive on halfway for SARS-CoV-2 and 122 discharged from hospital, compared specific antibodies, immune cells, and cytokine changes between the hospitalized and discharged patients. The hospitalized patients had a longer illness time compared with discharged patients. Analysis of viral loads explained long-term or persistent infection of SARS-CoV-2, which existed with the median time of 18.5 days of the positive nucleic acid test. Serum analysis showed that the specific anti-N IgG antibody was positive in all detected patients after infection of two weeks. Neutrophils, Monocytes, NK cells, and CD4(+) T cells significantly increased, while total lymphocytes and CD8(+) T cells decreased from non-critical hospitalized patients after longer-term infection. Further analysis of the cytokines showed that IL-6, TNF-α, IFN-γ, IL-2, IL-4, and IL-10 from the hospitalized patients were significantly higher, indicating a potential of the increased CD4(+) T cell differentiation. |
format | Online Article Text |
id | pubmed-7351676 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Published by Elsevier Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-73516762020-07-13 Long-term infection of SARS-CoV-2 changed the body's immune status Lin, Lan Luo, Shanshan Qin, Renjie Yang, Mengling Wang, Xiaobei Yang, Qianqian Zhang, Yang Wang, Quansheng Zhu, Rui Fan, Heng Wang, Haijun Hu, Yu Wang, Lin Hu, Desheng Clin Immunol Article The outbreak of SARS-CoV-2-associated pneumonia, a disease called COVID-19, has caused a pandemic worldwide. To investigate the immune responses after infection of SARS-CoV-2 in non-critical patients may help to better understand the disease progression. We collected 334 confirmed COVID-19 cases including 212 still in hospital with nucleic acid test positive on halfway for SARS-CoV-2 and 122 discharged from hospital, compared specific antibodies, immune cells, and cytokine changes between the hospitalized and discharged patients. The hospitalized patients had a longer illness time compared with discharged patients. Analysis of viral loads explained long-term or persistent infection of SARS-CoV-2, which existed with the median time of 18.5 days of the positive nucleic acid test. Serum analysis showed that the specific anti-N IgG antibody was positive in all detected patients after infection of two weeks. Neutrophils, Monocytes, NK cells, and CD4(+) T cells significantly increased, while total lymphocytes and CD8(+) T cells decreased from non-critical hospitalized patients after longer-term infection. Further analysis of the cytokines showed that IL-6, TNF-α, IFN-γ, IL-2, IL-4, and IL-10 from the hospitalized patients were significantly higher, indicating a potential of the increased CD4(+) T cell differentiation. Published by Elsevier Inc. 2020-09 2020-07-11 /pmc/articles/PMC7351676/ /pubmed/32659373 http://dx.doi.org/10.1016/j.clim.2020.108524 Text en © 2020 Published by Elsevier Inc. Since January 2020 Elsevier has created a COVID-19 resource centre with free information in English and Mandarin on the novel coronavirus COVID-19. The COVID-19 resource centre is hosted on Elsevier Connect, the company's public news and information website. Elsevier hereby grants permission to make all its COVID-19-related research that is available on the COVID-19 resource centre - including this research content - immediately available in PubMed Central and other publicly funded repositories, such as the WHO COVID database with rights for unrestricted research re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for free by Elsevier for as long as the COVID-19 resource centre remains active. |
spellingShingle | Article Lin, Lan Luo, Shanshan Qin, Renjie Yang, Mengling Wang, Xiaobei Yang, Qianqian Zhang, Yang Wang, Quansheng Zhu, Rui Fan, Heng Wang, Haijun Hu, Yu Wang, Lin Hu, Desheng Long-term infection of SARS-CoV-2 changed the body's immune status |
title | Long-term infection of SARS-CoV-2 changed the body's immune status |
title_full | Long-term infection of SARS-CoV-2 changed the body's immune status |
title_fullStr | Long-term infection of SARS-CoV-2 changed the body's immune status |
title_full_unstemmed | Long-term infection of SARS-CoV-2 changed the body's immune status |
title_short | Long-term infection of SARS-CoV-2 changed the body's immune status |
title_sort | long-term infection of sars-cov-2 changed the body's immune status |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7351676/ https://www.ncbi.nlm.nih.gov/pubmed/32659373 http://dx.doi.org/10.1016/j.clim.2020.108524 |
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