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About:
Immune alterations during SARS-CoV-2-related acute respiratory distress syndrome
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An Entity of Type :
schema:ScholarlyArticle
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covidontheweb.inria.fr
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Academic Article
research paper
schema:ScholarlyArticle
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type
Academic Article
research paper
schema:ScholarlyArticle
isDefinedBy
Covid-on-the-Web dataset
title
Immune alterations during SARS-CoV-2-related acute respiratory distress syndrome
Creator
Diehl, Jean-Luc
Bouadma, Lila
Thiébaut, Rodolphe
Hejblum, Boris
Wicky, Paul-Henri
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source
MedRxiv
abstract
We report a longitudinal analysis of the immune response associated with a fatal case of COVID-19. This patient exhibited a rapid evolution towards multiorgan failure. SARS-CoV-2 was detected in multiple nasopharyngeal, blood, and pleural samples, despite antiviral and immunomodulator treatment. Clinical evolution in the blood was marked by an increase (2-3 fold) in differentiated effector T cells expressing exhaustion (PD-1) and senescence (CD57) markers, an expansion of antibody-secreting cells, a 15-fold increase in {gamma}{delta} T-cell and proliferating NK-cell populations, and the total disappearance of monocytes, suggesting lung trafficking. In the serum, waves of a proinflammatory cytokine storm, Th1 and Th2 activation, and markers of T-cell exhaustion, apoptosis, cell cytotoxicity, and endothelial activation were observed until the fatal outcome. This case underscores the need for well-designed studies to investigate complementary approaches to control viral replication, the source of the hyperinflammatory status, and immunomodulation to target the pathophysiological response.
has issue date
2020-05-07
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bibo:doi
10.1101/2020.05.01.20087239
has license
medrxiv
sha1sum (hex)
cf267e85c23bd3786514713fc5ad29a03039d985
schema:url
https://doi.org/10.1101/2020.05.01.20087239
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Immune alterations during SARS-CoV-2-related acute respiratory distress syndrome
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covid:cf267e85c23bd3786514713fc5ad29a03039d985#body_text
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schema:about
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named entity 'cytotoxicity'
named entity 'Th1'
named entity 'ANTIVIRAL'
named entity 'IMMUNE RESPONSE'
named entity 'OBSERVED'
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