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Increased production of interleukin-10 in children with Down syndrome upon ex vivo stimulation with Streptococcus pneumoniae
被引:10
作者:
Broers, Chantal J. M.
[1
]
Gemke, Reinoud J. B. J.
[1
]
Morre, Servaas A.
[2
,3
]
Weijerman, Michel E.
[1
]
van Furth, Anne Marceline
[4
]
机构:
[1] Vrije Univ Amsterdam, Med Ctr, Dept Pediat, Amsterdam, Netherlands
[2] Vrije Univ Amsterdam, Med Ctr, Dept Med Microbiol & Infect Control, Immunogenet Lab, Amsterdam, Netherlands
[3] Univ Maastricht, Fac Hlth Med & Life Sci, Res Inst GROW, Inst Publ Hlth Genom,Dept Genet & Cell Biol, Maastricht, Netherlands
[4] Vrije Univ Amsterdam, Med Ctr, Dept Pediat Infect Dis Immunol & Rheumatol, Amsterdam, Netherlands
关键词:
COMMUNITY-ACQUIRED PNEUMONIA;
RESPIRATORY-TRACT INFECTIONS;
SYSTEMIC CYTOKINE RESPONSE;
INTRINSIC DEFECT;
PNEUMOCOCCAL PNEUMONIA;
IMMUNE-SYSTEM;
VIRUS;
IMMUNODEFICIENCY;
PREVALENCE;
TRISOMY-21;
D O I:
10.1038/pr.2013.173
中图分类号:
R72 [儿科学];
学科分类号:
100202 ;
摘要:
BACKGROUND: Children with Down syndrome (DS) have an increased susceptibility to infections, due to altered humoral and/or cellular immunity. The aim of the study was to determine the cytokine production in whole blood of children with DS upon stimulation with heat-killed Streptococcus pneumoniae and lipopolysaccharide (LPS), in comparison with their healthy siblings. METHODS: Whole blood of 61 children with DS and 57 of their healthy siblings was stimulated with 200 ng/ml LPS and 4x10(7) colony-forming units/ml S. pneumoniae during 6, 24, and 48 h. Concentrations of pro- and anti-inflammatory cytokines, tumor necrosis factor (TNF)-alpha, interleukin (IL)-1 beta, IL-6, IL-8, IL-12p70, and IL-10 were determined at all time points. RESULTS: Children with DS show an increased IL-10 production upon stimulation with S. pneumoniae compared to their healthy siblings. At most time points, no significant differences were seen in cytokine production upon stimulation with LPS. CONCLUSION: Children with DS may be prone to a severe course of pneumococcal pneumonia, because of an increased anti-inflammatory response.
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页码:109 / 113
页数:5
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