Frontiers in Immunology (Apr 2023)

Different degree of cytokinemia and T-cell activation according to serum IL-6 levels in critical COVID-19

  • Chan Mi Lee,
  • Minji Kim,
  • Minji Kim,
  • Minji Kim,
  • Chang Kyung Kang,
  • Pyoeng Gyun Choe,
  • Nam Joong Kim,
  • Hyeeun Bang,
  • Taeeun Cho,
  • Hyun Mu Shin,
  • Hyun Mu Shin,
  • Hyun Mu Shin,
  • Hang-Rae Kim,
  • Hang-Rae Kim,
  • Hang-Rae Kim,
  • Hang-Rae Kim,
  • Hang-Rae Kim,
  • Wan Beom Park,
  • Myoung-don Oh

DOI
https://doi.org/10.3389/fimmu.2023.1110874
Journal volume & issue
Vol. 14

Abstract

Read online

IntroductionTocilizumab, a humanized anti-interleukin-6 receptor (IL-6R) antibody, is recommended for the treatment of severe to critical coronavirus diseases 2019 (COVID-19). However, there were conflicting results on the efficacy of tocilizumab. Therefore, we hypothesized that the differences in tocilizumab efficacy may stem from the different immune responses of critical COVID-19 patients. In this study, we described two groups of immunologically distinct COVID-19 patients, based on their IL-6 response.MethodsWe prospectively enrolled critical COVID-19 patients, requiring oxygen support with a high flow nasal cannula or a mechanical ventilator, and analyzed their serial samples. An enzyme-linked immunosorbent assay and flow cytometry were used to evaluate the cytokine kinetics and cellular immune responses, respectively.ResultsA total of nine patients with critical COVID-19 were included. The high (n = 5) and low IL-6 (n = 4) groups were distinguished by their peak serum IL-6 levels, using 400 pg/mL as the cut-off value. Although the difference of flow cytometric data did not reach the level of statistical significance, the levels of pro-inflammatory cytokines and the frequencies of intermediate monocytes (CD14+CD16+), IFN-γ+ CD4+ or CD8+ T cells, and HLA-DR+PD-1+ CD4+ T cells were higher in the high IL-6 group than in the low IL-6 group.ConclusionThere were distinctive two groups of critical COVID-19 according to serum IL-6 levels having different degrees of cytokinemia and T-cell responses. Our results indicate that the use of immune modulators should be more tailored in patients with critical COVID-19.

Keywords