Department of Infectious Diseases and Clinical Microbiology, Kırıkkale University School of Medicine, Kırıkkale, Turkey.
J Microbiol Immunol Infect. 2013 Jun;46(3):158-63. doi: 10.1016/j.jmii.2012.05.008. Epub 2012 Oct 1.
CD14 is expressed principally by cells of monocyte/macrophage lineage and plays a pivotal role in the innate immunity to intracellular infections. Recent research findings have revealed an association between the CD14 gene promoter polymorphism and several major infectious diseases.
The aim of the present study was to investigate the association between the CD14-159C/T polymorphism and tuberculosis in a Turkish population.
For this purpose, 88 consecutive patients with tuberculosis (63 pulmonary, 25 extrapulmonary) and 116 control subjects were enrolled into a prospective study. We determined CD14-159 genotypes by polymerase chain reaction - restriction fragment length polymorphism analysis and also measured serum concentrations of soluble CD14 (sCD14) by using a quantitative sandwich enzyme immunoassay technique.
There was no significant difference in terms of genotype distribution between patients with tuberculosis (CC 18.2%, CT 48.9%, TT 33.0%) and controls (CC 12.9%, CT 50.9%, TT 36.2%) or between patients with pulmonary and extrapulmonary tuberculosis. Serum levels of sCD14 were significantly increased in patients with active tuberculosis compared to those with inactive tuberculosis and healthy controls (p<0.001). However, levels of sCD14 were not associated with any genotypes of CD14-159.
The genotyping findings of the present study do not support a role for the CD14-159C/T polymorphism in the development of tuberculosis, at least in the geographical region of central Anatolia. Significantly elevated serum sCD14 levels in patients with active disease reflect the importance of the mononuclear phagocytic system activation in tuberculosis.
CD14 主要表达于单核/巨噬细胞谱系细胞,在固有免疫针对细胞内感染中发挥关键作用。最近的研究发现 CD14 基因启动子多态性与多种主要传染病之间存在关联。
本研究旨在探讨土耳其人群中 CD14-159C/T 多态性与结核病之间的关系。
为此,前瞻性纳入 88 例连续结核病患者(63 例肺部,25 例肺外)和 116 例对照。我们通过聚合酶链反应-限制性片段长度多态性分析确定 CD14-159 基因型,并使用定量夹心酶免疫测定技术测定可溶性 CD14(sCD14)的血清浓度。
结核病患者(CC 18.2%,CT 48.9%,TT 33.0%)和对照组(CC 12.9%,CT 50.9%,TT 36.2%)之间基因型分布无显著差异,也无肺部和肺外结核病患者之间的差异。与非活动期结核病患者和健康对照组相比,活动期结核病患者的血清 sCD14 水平显著升高(p<0.001)。然而,sCD14 水平与 CD14-159 的任何基因型均无关。
本研究的基因分型结果不支持 CD14-159C/T 多态性在结核病发展中的作用,至少在安纳托利亚中部地区是如此。活动期疾病患者血清 sCD14 水平显著升高,反映了单核吞噬细胞系统激活在结核病中的重要性。