Dexamethasone Downregulates the Systemic Cytokine Response in Patients with Community-Acquired Pneumonia

Author:

Remmelts Hilde H. F.123,Meijvis Sabine C. A.1,Biesma Douwe H.14,van Velzen-Blad Heleen5,Voorn G. Paul5,Grutters Jan C.67,Bos Willem Jan W.1,Rijkers Ger T.58

Affiliation:

1. Department of Internal Medicine, St. Antonius Hospital, Nieuwegein, The Netherlands

2. Department of Internal Medicine, Gelderse Vallei, Ede, The Netherlands

3. Department of Internal Medicine and Infectious Diseases, University Medical Center Utrecht, Utrecht, The Netherlands

4. Department of Internal Medicine, University Medical Center Utrecht, Utrecht, The Netherlands

5. Department of Medical Microbiology and Immunology, St. Antonius Hospital, Nieuwegein, The Netherlands

6. Department of Pulmonology, St. Antonius Hospital, Nieuwegein, The Netherlands

7. Division of Heart & Lungs, University Medical Center Utrecht, Utrecht, The Netherlands

8. Department of Sciences, Roosevelt Academy, Middelburg, The Netherlands

Abstract

ABSTRACT The influence of adjunctive corticosteroids on the cytokine response in community-acquired pneumonia (CAP) is largely unknown. In this study, we analyzed the effect of dexamethasone on the cytokine response in patients with CAP and evaluated whether this effect is dependent on the causative microorganism. We hypothesized that dexamethasone has a larger effect on the cytokine response in patients with pneumococcal pneumonia than in patients with pneumonia caused by an atypical bacterium. A total of 304 hospitalized, nonimmunocompromised patients with CAP were randomized to an adjunctive 4-day course of 5 mg dexamethasone once a day ( n = 151) or a placebo ( n = 153). Serum concentrations of interleukin-1 receptor antagonist (IL-1Ra), IL-6, IL-8, IL-10, IL-17, tumor necrosis factor alpha (TNF-α), gamma interferon (IFN-γ), macrophage inflammatory protein-1 alpha (MIP-1α), and monocyte chemotactic protein-1 (MCP-1) were measured on days 0, 1, 2, and 4 and at a control visit. Overall, the concentrations of IL-6 ( P < 0.01), IL-8 ( P < 0.01), MCP-1 ( P < 0.01), and TNF-α ( P < 0.01) were significantly lower on day 2 in the dexamethasone group than in the placebo group. In patients with pneumococcal pneumonia ( n = 72), both treatment groups showed a rapid decrease of cytokine concentrations; only the concentration of TNF-α ( P = 0.05) was significantly lower in the dexamethasone group on day 2. In patients with CAP caused by an atypical pathogen ( Legionella pneumophila , Chlamydophila species, Coxiella burnetii , or Mycoplasma pneumoniae ; n = 58), IL-1Ra ( P < 0.01), IL-6 ( P < 0.01), and MCP-1 ( P = 0.03) decreased more rapidly in the dexamethasone group than in the placebo group. In conclusion, dexamethasone downregulates the cytokine response during CAP. This effect seems to be dependent on the causative microorganism. This study provides insight into which patients with CAP might benefit most from adjunctive dexamethasone.

Publisher

American Society for Microbiology

Subject

Microbiology (medical),Clinical Biochemistry,Immunology,Immunology and Allergy

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