Cytokines and their relationship with the severity and prognosis of coronavirus disease 2019 (COVID-19): a retrospective cohort study

BMJ Open. 2020 Nov 30;10(11):e041471. doi: 10.1136/bmjopen-2020-041471.

Abstract

Objective: To delineate the characteristics and clinical significance of plasma inflammatory cytokines altered in COVID-19.

Design: Retrospective, single-centre cohort study.

Setting: Tongji Hospital in Wuhan, China.

Participants: Among a cohort of 308 patients with a diagnosis of COVID-19, 138 patients died while 170 patients recovered and were discharged from the hospital. The data were collected until 27 February 2020.

Primary and secondary outcome measures: Clinical characteristics and laboratory findings were obtained from electronic medical records using data collection forms.

Results: The percentage of patients with elevated interleukin 2 receptor (IL-2R), IL-6, IL-8, IL-10 and tumour necrosis factor (TNF) increased with severity of disease (p<0.0001 for all). IL-2R (p<0.0001), IL-6 (p<0.0001), IL-8 (p=0.0001), IL-10 (p<0.0001) and TNF (p<0.0001) were also twofold to 20-fold higher in patients who died compared with those who recovered. Also, IL-6 and IL-10 increased in both the progressive patient groups: moderate (p=0.0026) and severe (p<0.0001). In multivariate analysis, higher levels of IL-2R (OR 1.001, 95% CI 1.000 to 1.002, p=0.031) and IL-6 (OR 1.013, 95% CI 1.003 to 1.024, p=0.015) on admission were associated with increasing odds of in-hospital death, independent of other covariates, including severity of disease and lymphocyte count.

Conclusion: Increased proinflammatory and anti-inflammatory cytokines, including IL-2R, IL-6, IL-8, TNF and IL-10, showed an obvious association with both COVID-19 severity and in-hospital mortality. Thus, our study indicates that cytokines are valuable in predicting the severity of COVID-19 and helps in distinguishing critically ill patients from the less affected ones.

Keywords: COVID-19; immunology; infection control; respiratory infections.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aged
  • COVID-19* / blood
  • COVID-19* / diagnosis
  • COVID-19* / mortality
  • China
  • Critical Illness*
  • Cytokines / blood*
  • Female
  • Hospital Mortality*
  • Hospitals
  • Humans
  • Inflammation / blood
  • Inflammation / etiology
  • Interleukin-10 / blood
  • Interleukin-2 Receptor alpha Subunit / blood
  • Lymphocyte Count
  • Male
  • Middle Aged
  • Pandemics
  • Prognosis
  • Retrospective Studies
  • SARS-CoV-2
  • Severity of Illness Index*
  • Tumor Necrosis Factor-alpha

Substances

  • Cytokines
  • IL10 protein, human
  • IL2RA protein, human
  • Interleukin-2 Receptor alpha Subunit
  • Tumor Necrosis Factor-alpha
  • Interleukin-10