Severe COVID-19 patients display hyper-activated NK cells and NK cell-platelet aggregates.
Humans
Granzymes
/ metabolism
COVID-19
Perforin
/ metabolism
Interleukin-15
/ metabolism
Interleukin-18
/ metabolism
SARS-CoV-2
Tumor Necrosis Factor-alpha
/ metabolism
Blood Platelets
/ metabolism
Integrin alpha1
/ metabolism
Killer Cells, Natural
Cytokines
/ metabolism
Chemokines
/ metabolism
Interleukin-12
/ metabolism
Antiviral Agents
/ metabolism
RNA
/ metabolism
COVID-19
NK cells
cytokines
cytotoxicity
platelet aggregates
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2022
2022
Historique:
received:
24
01
2022
accepted:
15
08
2022
entrez:
24
10
2022
pubmed:
25
10
2022
medline:
26
10
2022
Statut:
epublish
Résumé
COVID-19 is characterised by a broad spectrum of clinical and pathological features. Natural killer (NK) cells play an important role in innate immune responses to viral infections. Here, we analysed the phenotype and activity of NK cells in the blood of COVID-19 patients using flow cytometry, single-cell RNA-sequencing (scRNA-seq), and a cytotoxic killing assay. In the plasma of patients, we quantified the main cytokines and chemokines. Our cohort comprises COVID-19 patients hospitalised in a low-care ward unit (WARD), patients with severe COVID-19 disease symptoms hospitalised in intensive care units (ICU), and post-COVID-19 patients, who were discharged from hospital six weeks earlier. NK cells from hospitalised COVID-19 patients displayed an activated phenotype with substantial differences between WARD and ICU patients and the timing when samples were taken post-onset of symptoms. While NK cells from COVID-19 patients at an early stage of infection showed increased expression of the cytotoxic molecules perforin and granzyme A and B, NK cells from patients at later stages of COVID-19 presented enhanced levels of IFN-γ and TNF-α which were measured
Identifiants
pubmed: 36275702
doi: 10.3389/fimmu.2022.861251
pmc: PMC9581751
doi:
Substances chimiques
Granzymes
EC 3.4.21.-
Perforin
126465-35-8
Interleukin-15
0
Interleukin-18
0
Tumor Necrosis Factor-alpha
0
Integrin alpha1
0
Cytokines
0
Chemokines
0
Interleukin-12
187348-17-0
Antiviral Agents
0
RNA
63231-63-0
Types de publication
Journal Article
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
861251Informations de copyright
Copyright © 2022 Malengier-Devlies, Filtjens, Ahmadzadeh, Boeckx, Vandenhaute, De Visscher, Bernaerts, Mitera, Jacobs, Vanderbeke, Van Mol, Van Herck, Hermans, Meersseman, Wilmer, Gouwy, Garg, Humblet-Baron, De Smet, Martinod, Wauters, Proost, Wouters, Leclercq, Lambrechts, Wauters and Matthys.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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