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Chemokines and eicosanoids fuel the hyperinflammation within the lungs of patients with severe COVID-19.
Zaid, Younes; Doré, Étienne; Dubuc, Isabelle; Archambault, Anne-Sophie; Flamand, Olivier; Laviolette, Michel; Flamand, Nicolas; Boilard, Éric; Flamand, Louis.
Affiliation
  • Zaid Y; Biology Department, Faculty of Sciences, Mohammed V University in Rabat, Morocco; Cheikh Zaïd Hospital, Abulcasis University of Health Sciences, Rabat, Morocco.
  • Doré É; Axe Maladies Infectieuses et Immunitaires, Centre de Recherche du Centre Hospitalier Universitaire de Québec-Université Laval, Canada; Centre de Recherche Arthrite, Université Laval, Québec, Canada.
  • Dubuc I; Axe Maladies Infectieuses et Immunitaires, Centre de Recherche du Centre Hospitalier Universitaire de Québec-Université Laval, Canada.
  • Archambault AS; Centre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Québec, Faculté de Médecine, Département de Médecine, Université Laval, Québec City, Québec, Canada; Canada Research Excellence Chair in the Microbiome-Endocannabinoidome Axis in Metabolic Health, Université Laval, Q
  • Flamand O; Axe Maladies Infectieuses et Immunitaires, Centre de Recherche du Centre Hospitalier Universitaire de Québec-Université Laval, Canada.
  • Laviolette M; Centre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Québec, Faculté de Médecine, Département de Médecine, Université Laval, Québec City, Québec, Canada.
  • Flamand N; Centre de Recherche de l'Institut Universitaire de Cardiologie et de Pneumologie de Québec, Faculté de Médecine, Département de Médecine, Université Laval, Québec City, Québec, Canada; Canada Research Excellence Chair in the Microbiome-Endocannabinoidome Axis in Metabolic Health, Université Laval, Q
  • Boilard É; Axe Maladies Infectieuses et Immunitaires, Centre de Recherche du Centre Hospitalier Universitaire de Québec-Université Laval, Canada; Centre de Recherche Arthrite, Université Laval, Québec, Canada; Département de Microbiologie-Infectiologie et d'Immunologie, Université Laval, Québec City, Canada.
  • Flamand L; Axe Maladies Infectieuses et Immunitaires, Centre de Recherche du Centre Hospitalier Universitaire de Québec-Université Laval, Canada; Département de Microbiologie-Infectiologie et d'Immunologie, Université Laval, Québec City, Canada. Electronic address: louis.flamand@crchudequebec.ulaval.ca.
J Allergy Clin Immunol ; 148(2): 368-380.e3, 2021 08.
Article in En | MEDLINE | ID: mdl-34111453
ABSTRACT

BACKGROUND:

Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection can lead to a variety of clinical outcomes, ranging from the absence of symptoms to severe acute respiratory disease and ultimately death. A feature of patients with severe coronavirus disease 2019 (COVID-19) is the abundance of inflammatory cytokines in the blood. Elevated levels of cytokines are predictive of infection severity and clinical outcome. In contrast, studies aimed at defining the driving forces behind the inflammation in lungs of subjects with severe COVID-19 remain scarce.

OBJECTIVE:

Our aim was to analyze and compare the plasma and bronchoalveolar lavage (BAL) fluids of patients with severe COVID-19 (n = 45) for the presence of cytokines and lipid mediators of inflammation (LMIs).

METHODS:

Cytokines were measured by using Luminex multiplex assay, and LMIs were measured by using liquid chromatography-tandem mass spectrometry.

RESULTS:

We revealed high concentrations of numerous cytokines, chemokines, and LMIs in the BAL fluid of patients with severe COVID-19. Of the 13 most abundant mediators in BAL fluid, 11 were chemokines, with CXCL1 and CXCL8 being 200 times more abundant than IL-6 and TNF-α. Eicosanoid levels were also elevated in the lungs of subjects with severe COVID-19. Consistent with the presence chemotactic molecules, BAL fluid samples were enriched for neutrophils, lymphocytes, and eosinophils. Inflammatory cytokines and LMIs in plasma showed limited correlations with those present in BAL fluid, arguing that circulating inflammatory molecules may not be a reliable proxy of the inflammation occurring in the lungs of patients with severe COVID-19.

CONCLUSIONS:

Our findings indicate that hyperinflammation of the lungs of patients with severe COVID-19 is fueled by excessive production of chemokines and eicosanoids. Therapeutic strategies to dampen inflammation in patients with COVID-19 should be tailored accordingly.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Eicosanoids / Cytokines / SARS-CoV-2 / COVID-19 / Inflammation / Lung Type of study: Prognostic_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: J Allergy Clin Immunol Year: 2021 Document type: Article Affiliation country:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Eicosanoids / Cytokines / SARS-CoV-2 / COVID-19 / Inflammation / Lung Type of study: Prognostic_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Language: En Journal: J Allergy Clin Immunol Year: 2021 Document type: Article Affiliation country:
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