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Eosinophil-mediated lung inflammation associated with elevated natural killer T cell response in COVID-19 patients

Authors :
Nam Hyuk Cho
Da Young Kim
Na Ra Yun
Yeon Sook Kim
Yong Sub Na
Dong-Min Kim
Hyoree Park
Na Young Ha
Choon-Mee Kim
Yuri Kim
Sung Ho Yoon
Sung-Chul Lim
Uni Park
Jun-Won Seo
Do Sik Moon
Source :
The Korean Journal of Internal Medicine, The Korean Journal of Internal Medicine, Vol 37, Iss 1, Pp 201-209 (2022)
Publication Year :
2021
Publisher :
Korean Association of Internal Medicine, 2021.

Abstract

Background/Aims: Coronavirus disease 2019 (COVID-19) is associated with acute respiratory syndrome. The mechanisms underlying the different degrees of pneumonia severity in patients with COVID-19 remain elusive. This study provides evidence that COVID-19 is associated with eosinophil-mediated inflammation.Methods: We performed a retrospective case series of three patients with laboratory and radiologically confirmed COVID-19 pneumonia admitted to Chosun University Hospital. Demographic and clinical data on inflammatory cell lung infiltration and cytokine levels in patients with COVID-19 were collected.Results: Cytological analysis of sputum, tracheal aspirates, and bronchoalveolar lavage fluid (BALF) samples from all three patients revealed massive infiltration of polymorphonuclear cells (PMNs), such as eosinophils and neutrophils. All sputum and BALF specimens contained high levels of eosinophil cationic proteins. The infiltration of PMNs into the lungs, together with elevated levels of natural killer T (NKT) cells in BALF and peripheral blood samples from patients with severe pneumonia in the acute phase was confirmed by flow cytometry.Conclusions: These results suggest that the lungs of COVID-19 patients can exhibit eosinophil-mediated inflammation, together with an elevated NKT cell response, which is associated with COVID-19 pneumonia.

Details

Language :
English
ISSN :
20056648 and 12263303
Volume :
37
Issue :
1
Database :
OpenAIRE
Journal :
The Korean Journal of Internal Medicine
Accession number :
edsair.doi.dedup.....45086f3b88a7e12c6a934dee1640316c