Cargando…
Using IL‐2R/lymphocytes for predicting the clinical progression of patients with COVID‐19
Effective laboratory markers for the estimation of disease severity and predicting the clinical progression of coronavirus disease‐2019 (COVID‐19) is urgently needed. Laboratory tests, including blood routine, cytokine profiles and infection markers, were collected from 389 confirmed COVID‐19 patien...
Autores principales: | , , , , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7267633/ https://www.ncbi.nlm.nih.gov/pubmed/32365221 http://dx.doi.org/10.1111/cei.13450 |
_version_ | 1783541452111872000 |
---|---|
author | Hou, H. Zhang, B. Huang, H. Luo, Y. Wu, S. Tang, G. Liu, W. Mao, L. Mao, L. Wang, F. Sun, Z. |
author_facet | Hou, H. Zhang, B. Huang, H. Luo, Y. Wu, S. Tang, G. Liu, W. Mao, L. Mao, L. Wang, F. Sun, Z. |
author_sort | Hou, H. |
collection | PubMed |
description | Effective laboratory markers for the estimation of disease severity and predicting the clinical progression of coronavirus disease‐2019 (COVID‐19) is urgently needed. Laboratory tests, including blood routine, cytokine profiles and infection markers, were collected from 389 confirmed COVID‐19 patients. The included patients were classified into mild (n = 168), severe (n = 169) and critical groups (n = 52). The leukocytes, neutrophils, infection biomarkers [such as C‐reactive protein (CRP), procalcitonin (PCT) and ferritin] and the concentrations of cytokines [interleukin (IL)‐2R, IL‐6, IL‐8, IL‐10 and tumor necrosis factor (TNF)‐α] were significantly increased, while lymphocytes were significantly decreased with increased severity of illness. The amount of IL‐2R was positively correlated with the other cytokines and negatively correlated with lymphocyte number. The ratio of IL‐2R to lymphocytes was found to be remarkably increased in severe and critical patients. IL‐2R/lymphocytes were superior compared with other markers for the identification of COVID‐19 with critical illness, not only from mild but also from severe illness. Moreover, the cytokine profiles and IL‐2R/lymphocytes were significantly decreased in recovered patients, but further increased in disease‐deteriorated patients, which might be correlated with the outcome of COVID‐19. Lymphopenia and increased levels of cytokines were closely associated with disease severity. The IL‐2R/lymphocyte was a prominent biomarker for early identification of severe COVID‐19 and predicting the clinical progression of the disease. |
format | Online Article Text |
id | pubmed-7267633 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72676332020-06-03 Using IL‐2R/lymphocytes for predicting the clinical progression of patients with COVID‐19 Hou, H. Zhang, B. Huang, H. Luo, Y. Wu, S. Tang, G. Liu, W. Mao, L. Mao, L. Wang, F. Sun, Z. Clin Exp Immunol Original Articles Effective laboratory markers for the estimation of disease severity and predicting the clinical progression of coronavirus disease‐2019 (COVID‐19) is urgently needed. Laboratory tests, including blood routine, cytokine profiles and infection markers, were collected from 389 confirmed COVID‐19 patients. The included patients were classified into mild (n = 168), severe (n = 169) and critical groups (n = 52). The leukocytes, neutrophils, infection biomarkers [such as C‐reactive protein (CRP), procalcitonin (PCT) and ferritin] and the concentrations of cytokines [interleukin (IL)‐2R, IL‐6, IL‐8, IL‐10 and tumor necrosis factor (TNF)‐α] were significantly increased, while lymphocytes were significantly decreased with increased severity of illness. The amount of IL‐2R was positively correlated with the other cytokines and negatively correlated with lymphocyte number. The ratio of IL‐2R to lymphocytes was found to be remarkably increased in severe and critical patients. IL‐2R/lymphocytes were superior compared with other markers for the identification of COVID‐19 with critical illness, not only from mild but also from severe illness. Moreover, the cytokine profiles and IL‐2R/lymphocytes were significantly decreased in recovered patients, but further increased in disease‐deteriorated patients, which might be correlated with the outcome of COVID‐19. Lymphopenia and increased levels of cytokines were closely associated with disease severity. The IL‐2R/lymphocyte was a prominent biomarker for early identification of severe COVID‐19 and predicting the clinical progression of the disease. John Wiley and Sons Inc. 2020-05-15 2020-07 /pmc/articles/PMC7267633/ /pubmed/32365221 http://dx.doi.org/10.1111/cei.13450 Text en © 2020 British Society for Immunology |
spellingShingle | Original Articles Hou, H. Zhang, B. Huang, H. Luo, Y. Wu, S. Tang, G. Liu, W. Mao, L. Mao, L. Wang, F. Sun, Z. Using IL‐2R/lymphocytes for predicting the clinical progression of patients with COVID‐19 |
title | Using IL‐2R/lymphocytes for predicting the clinical progression of patients with COVID‐19 |
title_full | Using IL‐2R/lymphocytes for predicting the clinical progression of patients with COVID‐19 |
title_fullStr | Using IL‐2R/lymphocytes for predicting the clinical progression of patients with COVID‐19 |
title_full_unstemmed | Using IL‐2R/lymphocytes for predicting the clinical progression of patients with COVID‐19 |
title_short | Using IL‐2R/lymphocytes for predicting the clinical progression of patients with COVID‐19 |
title_sort | using il‐2r/lymphocytes for predicting the clinical progression of patients with covid‐19 |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7267633/ https://www.ncbi.nlm.nih.gov/pubmed/32365221 http://dx.doi.org/10.1111/cei.13450 |
work_keys_str_mv | AT houh usingil2rlymphocytesforpredictingtheclinicalprogressionofpatientswithcovid19 AT zhangb usingil2rlymphocytesforpredictingtheclinicalprogressionofpatientswithcovid19 AT huangh usingil2rlymphocytesforpredictingtheclinicalprogressionofpatientswithcovid19 AT luoy usingil2rlymphocytesforpredictingtheclinicalprogressionofpatientswithcovid19 AT wus usingil2rlymphocytesforpredictingtheclinicalprogressionofpatientswithcovid19 AT tangg usingil2rlymphocytesforpredictingtheclinicalprogressionofpatientswithcovid19 AT liuw usingil2rlymphocytesforpredictingtheclinicalprogressionofpatientswithcovid19 AT maol usingil2rlymphocytesforpredictingtheclinicalprogressionofpatientswithcovid19 AT maol usingil2rlymphocytesforpredictingtheclinicalprogressionofpatientswithcovid19 AT wangf usingil2rlymphocytesforpredictingtheclinicalprogressionofpatientswithcovid19 AT sunz usingil2rlymphocytesforpredictingtheclinicalprogressionofpatientswithcovid19 |