A Granulocytic Signature Identifies COVID-19 and Its Severity. (17th September 2020)
- Record Type:
- Journal Article
- Title:
- A Granulocytic Signature Identifies COVID-19 and Its Severity. (17th September 2020)
- Main Title:
- A Granulocytic Signature Identifies COVID-19 and Its Severity
- Authors:
- Vitte, Joana
Diallo, Aïssatou Bailo
Boumaza, Asma
Lopez, Alexandre
Michel, Moïse
Allardet-Servent, Jérôme
Mezouar, Soraya
Sereme, Youssouf
Busnel, Jean-Marc
Miloud, Tewfik
Malergue, Fabrice
Morange, Pierre-Emmanuel
Halfon, Philippe
Olive, Daniel
Leone, Marc
Mege, Jean-Louis - Abstract:
- Abstract: Background: An unbiased approach to SARS-CoV-2–induced immune dysregulation has not been undertaken so far. We aimed to identify previously unreported immune markers able to discriminate COVID-19 patients from healthy controls and to predict mild and severe disease. Methods: An observational, prospective, multicentric study was conducted in patients with confirmed mild/moderate (n = 7) and severe (n = 19) COVID-19. Immunophenotyping of whole-blood leukocytes was performed in patients upon hospital ward or intensive care unit admission and in healthy controls (n = 25). Clinically relevant associations were identified through unsupervised analysis. Results: Granulocytic (neutrophil, eosinophil, and basophil) markers were enriched during COVID-19 and discriminated between patients with mild and severe disease. Increased counts of CD15 + CD16 + neutrophils, decreased granulocytic expression of integrin CD11b, and Th2-related CRTH2 downregulation in eosinophils and basophils established a COVID-19 signature. Severity was associated with emergence of PD-L1 checkpoint expression in basophils and eosinophils. This granulocytic signature was accompanied by monocyte and lymphocyte immunoparalysis. Correlation with validated clinical scores supported pathophysiological relevance. Conclusions: Phenotypic markers of circulating granulocytes are strong discriminators between infected and uninfected individuals as well as between severity stages. COVID-19 alters the frequency andAbstract: Background: An unbiased approach to SARS-CoV-2–induced immune dysregulation has not been undertaken so far. We aimed to identify previously unreported immune markers able to discriminate COVID-19 patients from healthy controls and to predict mild and severe disease. Methods: An observational, prospective, multicentric study was conducted in patients with confirmed mild/moderate (n = 7) and severe (n = 19) COVID-19. Immunophenotyping of whole-blood leukocytes was performed in patients upon hospital ward or intensive care unit admission and in healthy controls (n = 25). Clinically relevant associations were identified through unsupervised analysis. Results: Granulocytic (neutrophil, eosinophil, and basophil) markers were enriched during COVID-19 and discriminated between patients with mild and severe disease. Increased counts of CD15 + CD16 + neutrophils, decreased granulocytic expression of integrin CD11b, and Th2-related CRTH2 downregulation in eosinophils and basophils established a COVID-19 signature. Severity was associated with emergence of PD-L1 checkpoint expression in basophils and eosinophils. This granulocytic signature was accompanied by monocyte and lymphocyte immunoparalysis. Correlation with validated clinical scores supported pathophysiological relevance. Conclusions: Phenotypic markers of circulating granulocytes are strong discriminators between infected and uninfected individuals as well as between severity stages. COVID-19 alters the frequency and functional phenotypes of granulocyte subsets with emergence of CRTH2 as a disease biomarker. Abstract : Unsupervised mapping of leukocyte surface markers identified a granulocytic COVID-19 signature comprising eosinophil and basophil CRTH2 downregulation, increased counts of CD15 + CD16 + neutrophils, and decreased granulocytic CD11b expression, while PD-L1 checkpoint expression in basophils and eosinophils was associated with severity. … (more)
- Is Part Of:
- Journal of infectious diseases. Volume 222:Number 12(2020)
- Journal:
- Journal of infectious diseases
- Issue:
- Volume 222:Number 12(2020)
- Issue Display:
- Volume 222, Issue 12 (2020)
- Year:
- 2020
- Volume:
- 222
- Issue:
- 12
- Issue Sort Value:
- 2020-0222-0012-0000
- Page Start:
- 1985
- Page End:
- 1996
- Publication Date:
- 2020-09-17
- Subjects:
- SARS-CoV-2 -- COVID-19 -- neutrophil -- eosinophil -- basophil -- CRTH2 -- immune checkpoint -- CD11b -- CD16 -- PD-L1
Communicable diseases -- Periodicals
Diseases -- Causes and theories of causation -- Periodicals
Medicine -- Periodicals
Communicable Diseases -- Periodicals
Electronic journals
616.9 - Journal URLs:
- http://jid.oxfordjournals.org/content/by/year ↗
http://www.journals.uchicago.edu/JID/journal/ ↗
http://www.jstor.org/journals/00221899.html ↗
http://ukcatalogue.oup.com/ ↗ - DOI:
- 10.1093/infdis/jiaa591 ↗
- Languages:
- English
- ISSNs:
- 0022-1899
- Deposit Type:
- Legaldeposit
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- Available online (eLD content is only available in our Reading Rooms) ↗
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- British Library DSC - 5006.700000
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