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About:
Suppressed T cell-mediated immunity in patients with COVID-19: a clinical retrospective study in Wuhan, China
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schema:ScholarlyArticle
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covidontheweb.inria.fr
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Type:
Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
title
Suppressed T cell-mediated immunity in patients with COVID-19: a clinical retrospective study in Wuhan, China
Creator
Miao, Qing
Xu, Bo
Cong, He△
Fan, Cun-Yu
Fan△, Cun-Yu
He, Cong
Miao☆, Qing
Other, ;
Wang, An-Lu
Wang☆, An-Lu
Xia, Wen-Guang
Xia△, Wen-Guang
Xu△, Bo
Yu, Yi-Han
Yu△, Yi-Han
Zhang, Ji-Xian
Zhang△, Ji-Xian
Zou, Yi-Long
Zou△, Yi-Long
source
Elsevier; Medline; PMC
abstract
Abstract Importance An ongoing outbreak of COVID-19 has exhibited significant threats around the world. We found a significant decrease of T lymphocyte subsets and an increase of inflammatory cytokines of hospitalized patients with COVID-19 in clinical practice. Methods We conducted a retrospective, single-center observational study of in-hospital adult patients with confirmed COVID-19 in Hubei Provincial Hospital of traditional Chinese and Western medicine (Wuhan, China) by Mar 1, 2020. Demographic, clinical, laboratory information, especially T lymphocyte subsets and inflammatory cytokines were reported. For patients who died or discharge from hospital, the associations of T lymphocyte subsets on admission were evaluated by univariate logistic regression with odds ratios (ORs) and 95% confidence intervals (CIs), warning values to predict in-hospital death were assessed by Receiver Operator Characteristic (ROC) curves. Results A total of 187 patients were enrolled in our study from Dec 26, 2019 to Mar 1, 2020, of whom 145 were survivors (discharge= 117) or non-survivors (in-hospital death=28). All patients exhibited a significant drop of T lymphocyte subsets counts with remarkably increasing concentrations of SAA, CRP, IL-6, and IL-10 compared to normal values. The median concentrations of SAA and CRP in critically-ill patients were nearly 4- and 10-fold than those of mild-ill patients, respectively. As the severity of COVID-19 getting worse, the counts of T lymphocyte drop lower.28 patients died in hospital, the median lymphocyte, CD3+ T-cell, CD4+ T-cell, CD8+ T-cell and B-cell were significantly lower than other patients. Lower counts (/uL) of T lymphocyte subsets lymphocyte (<500), CD3+T-cell (<200), CD4+ T-cell (<100), CD8+ T-cell (<100) and B-cell (<50) were associated with higher risks of in-hospital death of CIVID-19. The warning values to predict in-hospital death of lymphocyte, CD3+ T-cell, CD4+ T-cell, CD8+ T-cell, and B-cell were 559, 235, 104, 85 and 82, respectively. Conclusion We find a significant decrease of T lymphocyte subset is positively correlated with in-hospital death and severity of illness. The decreased levels of T lymphocyte subsets reported in our study were similar with SARS but not common among other virus infection, which may be possible biomarkers for early diagnosis of COVID-19. Our findings may shed light on early warning of high risks of mortality and help early intervention and treatment of COVID-19.
has issue date
2020-04-18
(
xsd:dateTime
)
bibo:doi
10.1016/j.jinf.2020.04.012
bibo:pmid
32315725
has license
els-covid
sha1sum (hex)
34bb7c0b70a65346092067f7c0983de1f92ef5e2
schema:url
https://doi.org/10.1016/j.jinf.2020.04.012
resource representing a document's title
Suppressed T cell-mediated immunity in patients with COVID-19: a clinical retrospective study in Wuhan, China
has PubMed Central identifier
PMC7166040
has PubMed identifier
32315725
schema:publication
J Infect
resource representing a document's body
covid:34bb7c0b70a65346092067f7c0983de1f92ef5e2#body_text
is
schema:about
of
named entity 'lymphocyte subsets'
named entity 'cell-mediated immunity'
named entity 'FOUND'
named entity 'WORLD'
named entity 'COVID-19'
named entity 'Suppressed'
named entity 'Wuhan'
named entity 'Wuhan'
named entity 'CRP'
named entity 'T-cell'
named entity 'yu FAN'
named entity 'COVID'
named entity 'coronavirus disease'
named entity 'coronavirus infection'
named entity 'B-cell'
named entity 'Center for Disease Control and Prevention'
named entity 'T lymphocyte'
named entity 'lymphocyte'
named entity 'Hubei'
named entity 'B-cell'
named entity 'clinical symptoms'
named entity 'clinical outcomes'
named entity 'clinical studies'
named entity 'laboratory tests'
named entity 'virus infection'
named entity 'China'
named entity 'IL-10'
named entity 'sample size'
named entity 'SAA'
named entity 'complete blood count'
named entity 'infection'
named entity 'CD4 +'
named entity 'CD3'
named entity 'creatine kinase'
named entity 'COVID'
named entity 'ROC curve'
named entity 'cytokines'
named entity 'yu FAN'
named entity 'CD19'
named entity 'Middle East'
named entity 'flow cytometry'
named entity 'respiratory support'
named entity 'SAA'
named entity 'CD3'
named entity 'CD8 +'
named entity 'COVID'
named entity 'computed tomographic'
named entity 'CD4+ T-cell'
named entity 'CD8+ T-cell'
named entity 'observational study'
named entity 'lymphocyte subsets'
named entity 'virus'
named entity 'IL-6'
named entity 'lymphocyte subsets'
named entity 'T lymphocyte'
named entity 'liver function'
named entity 'risk factors'
named entity 'virus'
named entity 'CD8+ T-cell'
named entity 'amyloid'
named entity 'intensive care unit'
named entity 'logistic regression'
named entity 'COVID'
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