Cytokine response in pediatric patients with pandemic influenza H1N1 2009 virus infection and pneumonia: comparison with pediatric pneumonia without H1N1 2009 infection
- Author(s)
- Yeo Hyang Kim; Jung-Eun Kim; Myung Chul Hyun
- Keimyung Author(s)
- Kim, Yeo Hyang
- Department
- Dept. of Pediatrics (소아청소년학)
- Journal Title
- Pediatric Pulmonology
- Issued Date
- 2011
- Volume
- 46
- Issue
- 12
- Keyword
- children; influenza A virus; H1N1 subtype; pneumonia; cytokine; immunity; innate
- Abstract
- Objectives: We investigated serum cytokine levels in pediatric patients with pandemic
influenza H1N1 2009 virus (H1N1) infection-pneumonia and in pediatric patients with
pneumonia but without H1N1 infection, and examined correlations between cytokine levels and
clinical/laboratory findings. Methods: Fifty-seven cases of infection by H1N1 were confirmed by
RT-PCR and enrolled. Of these 57 cases, 26 had a severe H1N1 infection (group 1), and 31
had a mild H1N1 infection (group 2). Sera from 18 cases with pneumonia without H1N1 infection
(group 3) were used as controls. The serum levels of 10 cytokines were determined by
multiplex assay. Results: The serum levels of IFN-a, IL-6, and IP-10 were significantly higher in
H1N1 infected cases than in group 3, and levels of IL-6 and IP-10 were significantly higher
in group 1 than in group 2. The level of IL-10 was significantly higher in groups 1 and 3 than in
group 2. However, levels of IFN-g and IL-17 were not significantly different between the three
groups. IL-1b, IL-4, and MIP-1a were not detectable in most patients. IP-10 and IL-6 levels
were found to show negative correlations with lymphocyte count and oxygen saturation. Conclusions:
We found higher levels of cytokines (IFN-a, IL-6, IP-10) of innate immunity than those
of acquired immunity in pediatric H1N1 infection. Of the cytokines found to be increased in
cases with H1N1 infection, IP-10 and IL-6 were found to be correlated with disease severity
(lymphopenia and hypoxia). IP-10 and IL-6 may be important markers in pediatric H1N1 infection.
Pediatr Pulmonol. 2011;46:1233–1239. 2011 Wiley Periodicals,Inc.
Key words: children; influenza A virus; H1N1 subtype; pneumonia; cytokine; immunity;
innate.
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