Genetic variation in pro-inflammatory cytokines and meningococcal sepsis

被引:14
作者
Deasy, Alice [1 ]
Read, Robert C. [1 ]
机构
[1] Royal Hallamshire Hosp, Dept Infect & Immun, Sheffield Sch Med & Biomed Sci, Sheffield S10 3JF, S Yorkshire, England
关键词
cytokines; interleukin-1; meningococcal disease; polymorphism; single nucleotide; tumour necrosis factor; TUMOR-NECROSIS-FACTOR; FACTOR-ALPHA PROMOTER; RECEPTOR ANTAGONIST; SEPTIC SHOCK; DISEASE; INTERLEUKIN-1; POLYMORPHISM; SUSCEPTIBILITY; ASSOCIATION; SEVERITY;
D O I
10.1097/QCO.0b013e32833939de
中图分类号
R51 [传染病];
学科分类号
100201 [内科学];
摘要
Purpose of review Pro-inflammatory cytokines are an essential component of host defence in patients who are susceptible to meningococcal disease. This review summarizes what is currently known about genetic variations in genes encoding these defensive proteins and focuses on recent work investigating the potential role polymorphisms may play in susceptibility and severity of the disease. Recent findings A recently developed porcine model revealed significant cytokine derangement early in severe meningococcal sepsis raising the suggestion of a causative role for maladaptive cytokine release in the disease course. In patients who survive septic shock caused by the meningococcus there is a low innate production capacity for interleukin-1 beta. Several polymorphisms have been identified in genes encoding for pro-inflammatory cytokines, and recently studies have shown association with susceptibility to infection in polymorphism at both IL-1RA (+2018) and TNF (-308). Summary Recent work is adding to the growing evidence that genetic variation in pro-inflammatory cytokines has a role in susceptibility and survival in meningococcal disease. However, data need to be interpreted with caution as there are many confounding factors, sample sizes are often small and there are challenges in identifying suitable control groups.
引用
收藏
页码:255 / 258
页数:4
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