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Cytokine and chemokine profiles in the sera of COVID-19 patients with different stages of severity.

Authors :
Bourhis, Maryam
Idir, Abderrazak
Machraoui, Safa
Hachimi, Abdelhamid
Elouardi, Youssef
Jamil, Oumayma
Khallouki, Mohammed
Zahlane, Kawtar
Guennouni, Morad
Hazime, Raja
Essaadouni, Lamiaa
Lourhlam, Bouchra
Ennaji, Moulay Mustapha
Mouse, Hassan Ait
Admou, Brahim
Zyad, Abdelmajid
Source :
Cytokine. Aug2024, Vol. 180, pN.PAG-N.PAG. 1p.
Publication Year :
2024

Abstract

• COVID-19 asymptomatic patients had high levels of IL-8. • IL-12, IL-2, IL-13, IL-17 and GM-CSF were undetectable in COVID-19 asymptomatic patients. • IL-6, IL-10, MIP-1α, MCP-1 and IP-10 are associated with COVID-19 disease progression. • IL-4 tends to decrease with COVID-19 disease progression. • SARS-CoV-2 is associated with the cytokine storm. COVID-19 is a viral infection that disturbs the host's immune system and causes an overproduction of cytokines leading to a cytokine storm. The present study aimed to evaluate the serum levels of 27 protein biomarkers to determine their association with COVID-19 disease severity. The serum levels of 89 patients with different degrees of COVID-19 disease severity [asymptomatic (n = 14), moderate (n = 14), severe (n = 30), and critical (n = 31)] and 14 healthy individuals were tested for a panel of 27 cytokines and chemokines using Luminex assay (27 Bio‑Plex Pro Human Cytokine, Bio-rad™). IL-12, IL-2 and IL-13, as well as IL-17 and GM-CSF were clearly undetectable in asymptomatic patients. IL-8 levels were higher in asymptomatic compared with other groups. Very high levels of IL-6, IL-10 and the chemokines MIP-1α, MCP-1 and IP10 were associated with disease progression, while IL-4 tends to decrease with disease severity. Our study provides more evidence that excessive cytokine synthesis is linked to the disease progression. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
10434666
Volume :
180
Database :
Academic Search Index
Journal :
Cytokine
Publication Type :
Academic Journal
Accession number :
177908257
Full Text :
https://doi.org/10.1016/j.cyto.2024.156653