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Eosinophil-mediated lung inflammation associated with elevated natural killer T cell response in COVID-19 patients.
Kim, Dong-Min; Seo, Jun-Won; Kim, Yuri; Park, Uni; Ha, Na-Young; Park, Hyoree; Yun, Na Ra; Kim, Da Young; Yoon, Sung Ho; Na, Yong Sub; Moon, Do Sik; Lim, Sung-Chul; Kim, Choon-Mee; Kim, Yeon-Sook; Cho, Nam-Hyuk.
  • Kim DM; Department of Internal Medicine, Chosun University College of Medicine, Gwangju, Korea.
  • Seo JW; Department of Internal Medicine, Chosun University College of Medicine, Gwangju, Korea.
  • Kim Y; Department of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, Korea.
  • Park U; Department of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, Korea.
  • Ha NY; Department of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, Korea.
  • Park H; Department of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, Korea.
  • Yun NR; Department of Internal Medicine, Chosun University College of Medicine, Gwangju, Korea.
  • Kim DY; Department of Internal Medicine, Chosun University College of Medicine, Gwangju, Korea.
  • Yoon SH; Department of Internal Medicine, Chosun University College of Medicine, Gwangju, Korea.
  • Na YS; Department of Internal Medicine, Chosun University College of Medicine, Gwangju, Korea.
  • Moon DS; Department of Internal Medicine, Chosun University College of Medicine, Gwangju, Korea.
  • Lim SC; Department of Pathology, Chosun University College of Medicine, Gwangju, Korea.
  • Kim CM; Department of Premedical Science, Chosun University College of Medicine, Gwangju, Korea.
  • Kim YS; Department of Internal Medicine, Chungnam National University College of Medicine, Daejeon, Korea.
  • Cho NH; Department of Microbiology and Immunology, Seoul National University College of Medicine, Seoul, Korea.
Korean J Intern Med ; 37(1): 201-209, 2022 01.
Article in English | MEDLINE | ID: covidwho-1441243
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.

CONCLUSION:

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.
Subject(s)
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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pulmonary Eosinophilia / Natural Killer T-Cells / COVID-19 Type of study: Diagnostic study / Observational study / Prognostic study Limits: Humans Language: English Journal: Korean J Intern Med Journal subject: Internal Medicine Year: 2022 Document Type: Article

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Full text: Available Collection: International databases Database: MEDLINE Main subject: Pulmonary Eosinophilia / Natural Killer T-Cells / COVID-19 Type of study: Diagnostic study / Observational study / Prognostic study Limits: Humans Language: English Journal: Korean J Intern Med Journal subject: Internal Medicine Year: 2022 Document Type: Article