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Published on: August 7, 2017
Decreased interleukin-18 response in asthmatic children with severe Mycoplasma pneumoniae pneumonia
Hai Lee Chung1, Jin Young Shin, Mi Ju
1Department of Pediatrics, School of Medicine, Catholic University of Taegu, Taegu, South Korea. hlchung@cu.ac.kr
Purpose:
Mycoplasma pneumoniae (M. pneumoniae) is a common causative agent of pneumonia in children. The aim of this study is to determine whether there is any difference in selected cytokine or chemokines response in asthmatic children compared to non-asthmatic children during acute M. pneumoniae pneumonia.
Methods:
Seventy-five children, 6-12 years of age, admitted with M. pneumoniae pneumonia were enrolled. Two patient groups were defined: the children with known asthma (N=40) and non-asthmatic children (N=35). Interleukin (IL)-18 and selected chemokines, IL-8, CXCL9, CXCL10, and regulation upon activation normal T-cell expressed and secreted (RANTES) were measured by means of ELISA in the plasma samples of the patients collected on admission. We investigated the values of these mediators in relation to the asthma status and symptom severity of the patients. Twenty age-matched, non-infected controls were also studied.
Results:
Plasma levels of IL-18 and the chemokines increased significantly in the patients with M. pneumoniae pneumonia compared to non-infected, age-matched controls (P<0.01). However, the asthmatic patients showed significantly reduced IL-18 and CXCL10 responses (P<0.01, <0.05, respectively) and had more severe pneumonia symptoms (P<0.01) compared to non-asthmatic patients. IL-18 was significantly lower in severe pneumonia group than in non-severe group (P<0.05).
Conclusions:
Our study suggests that IL-18 and the chemokines are importantly involved in the pathogenesis of M. pneumoniae pneumonia. It also indicates that some asthmatic children have deficient IL-18 response when affected by M. pneumoniae pneumonia, which might be associated with more severe pneumonia observed in this group of patients.
Insights
Asthmatic children with Mycoplasma pneumoniae pneumonia showed reduced Interleukin-18 (IL-18) and CXCL10 responses, correlating with more severe symptoms. This suggests a deficient IL-18 response may contribute to worse outcomes in these patients.
Area of Science:
- Pediatric Infectious Diseases
- Immunology
- Respiratory Medicine
Background:
- Mycoplasma pneumoniae is a frequent cause of childhood pneumonia.
- Asthma is a common chronic respiratory condition in children.
- Understanding immune responses in pediatric pneumonia is crucial for effective treatment.
Purpose of the Study:
- To compare cytokine and chemokine responses in asthmatic versus non-asthmatic children with acute M. pneumoniae pneumonia.
- To investigate the relationship between immune mediators and symptom severity in pediatric M. pneumoniae pneumonia.
- To identify potential differences in immune profiles that could explain varied clinical outcomes.
Main Methods:
- Seventy-five children (6-12 years) with M. pneumoniae pneumonia were divided into asthmatic (N=40) and non-asthmatic (N=35) groups.
- Plasma levels of Interleukin-18 (IL-18) and chemokines (IL-8, CXCL9, CXCL10, RANTES) were measured using ELISA.
- Comparison of mediator levels and symptom severity between asthmatic and non-asthmatic patients, with 20 controls.
Main Results:
- Patients with M. pneumoniae pneumonia had significantly elevated IL-18 and chemokines compared to controls.
- Asthmatic children exhibited significantly lower IL-18 and CXCL10 levels.
- Asthmatic patients presented with more severe pneumonia symptoms, and lower IL-18 levels correlated with severity.
Conclusions:
- IL-18 and chemokines play a role in the pathogenesis of M. pneumoniae pneumonia.
- Asthmatic children may have a deficient IL-18 response during M. pneumoniae infection.
- This deficient response could be linked to the increased pneumonia severity observed in asthmatic children.
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