Plasma inflammatory cytokines and chemokines in severe acute respiratory syndrome

By C. Wong, C. Lam, A. Wu, W. Ip, N. Lee, I. Chan, L. Lit, D. Hui, M. Chan, S. Chung and 1 more. Clinical and Experimental Immunology, 2004

1,233 citations recorded by the source corpus.

Severe acute respiratory syndrome (SARS) is a recently emerged infectious disease caused by a novel coronavirus, but its immunopathological mechanisms have not yet been fully elucidated. We investigated changes in plasma T helper (Th) cell cytokines, inflammatory cytokines and chemokines in 20 patients diagnosed with SARS. Cytokine profile of SARS patients showed marked elevation of Th1 cytokine interferon (IFN)‐γ, inflammatory cytokines interleukin (IL)‐1, IL‐6 and IL‐12 for at least 2 weeks after disease onset, but there was no significant elevation of inflammatory cytokine tumour necrosis factor (TNF)‐α, anti‐inflammatory cytokine IL‐10, Th1 cytokine IL‐2 and Th2 cytokine IL‐4. The chemokine profile demonstrated significant elevation of neutrophil chemokine IL‐8, monocyte chemoattractant protein‐1 (MCP‐1), and Th1 chemokine IFN‐γ‐inducible protein‐10 (IP‐10). Corticosteroid reduced significantly IL‐8, MCP‐1 and IP‐10 concentrations from 5 to 8 days after treatment (all P < 0·001). Together, the elevation of Th1 cytokine IFN‐γ, inflammatory cytokines IL‐1, IL‐6 and IL‐12 and chemokines IL‐8, MCP‐1 and IP‐10 confirmed the activation of Th1 cell‐mediated immunity and hyperinnate inflammatory response in SARS through the accumulation of monocytes/macrophages and neutrophils.

View Paper: https://www.semanticscholar.org/paper/f9eee4c2021eabe3aa8d3102d5f8dc6000d0dcdf

How researchers see this paper

The researchers whose trusted networks rank it highest, strongest advocate first. Every researcher gets a different order.

  1. Jason Netland
  2. S. Weiss
  3. Susanna K. P. Lau
  4. V. Cheng
  5. Kwok-Yung Yuen
  6. Shasha Liu
  7. M. Iddir
  8. J. Leibowitz

Citations in the corpus