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American journal of respiratory and critical care medicine · 2020

Characterization of the Inflammatory Response to Severe COVID-19 Illness.

СтатьяНазвание и аннотация: Перевод пока не подготовлен
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McElvaney Oliver J, McEvoy Natalie L, McElvaney Oisín F, Carroll Tomás P, Murphy Mark P, Dunlea Danielle M, Ní Choileáin Orna, Clarke Jennifer, O'Connor Eoin, Hogan Grace, Ryan Daniel, Sulaiman Imran, Gunaratnam Cedric, Branagan Peter, O'Brien Michael E, Morgan Ross K, Costello Richard W, Hurley Killian, Walsh Seán, de Barra Eoghan, McNally Cora, McConkey Samuel, Boland Fiona, Galvin Sinead, Kiernan Fiona, O'Rourke James, Dwyer Rory, Power Michael, Geoghegan Pierce, Larkin Caroline, O'Leary Ruth Aoibheann, Freeman James, Gaffney Alan, Marsh Brian, Curley Gerard F, McElvaney Noel G

Аннотация

Rationale: Coronavirus disease (COVID-19) is a global threat to health. Its inflammatory characteristics are incompletely understood.Objectives: To define the cytokine profile of COVID-19 and to identify evidence of immunometabolic alterations in those with severe illness.Methods: Levels of IL-1β, IL-6, IL-8, IL-10, and sTNFR1 (soluble tumor necrosis factor receptor 1) were assessed in plasma from healthy volunteers, hospitalized but stable patients with COVID-19 (COVIDstable patients), patients with COVID-19 requiring ICU admission (COVIDICU patients), and patients with severe community-acquired pneumonia requiring ICU support (CAPICU patients). Immunometabolic markers were measured in circulating neutrophils from patients with severe COVID-19. The acute phase response of AAT (alpha-1 antitrypsin) to COVID-19 was also evaluated.Measurements and Main Results: IL-1β, IL-6, IL-8, and sTNFR1 were all increased in patients with COVID-19. COVIDICU patients could be clearly differentiated from COVIDstable patients, and demonstrated higher levels of IL-1β, IL-6, and sTNFR1 but lower IL-10 than CAPICU patients. COVID-19 neutrophils displayed altered immunometabolism, with increased cytosolic PKM2 (pyruvate kinase M2), phosphorylated PKM2, HIF-1α (hypoxia-inducible factor-1α), and lactate. The production and sialylation of AAT increased in COVID-19, but this antiinflammatory response was overwhelmed in severe illness, with the IL-6:AAT ratio markedly higher in patients requiring ICU admission (P < 0.0001). In critically unwell patients with COVID-19, increases in IL-6:AAT predicted prolonged ICU stay and mortality, whereas improvement in IL-6:AAT was associated with clinical resolution (P < 0.0001).Conclusions: The COVID-19 cytokinemia is distinct from that of other types of pneumonia, leading to organ failure and ICU need. Neutrophils undergo immunometabolic reprogramming in severe COVID-19 illness. Cytokine ratios may predict outcomes in this population.

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