Dauletbaev Nurlan, Gropp Roswitha, Frye Michaela, Loitsch Stefan, Wagner Thomas-Otto-Friedrich, Bargon Joachim
Pulmonary Medicine, Second Department of Internal Medicine, University Hospital, Johann Wolfgang Goethe University, Frankfurt/Main, Germany.
Respiration. 2002;69(1):46-51. doi: 10.1159/000049369.
Lack or inactivation of defensins may facilitate chronic bacterial colonization in the cystic fibrosis (CF) lung. CF nasal epithelium exhibits typical biochemical abnormalities and can be used to study defensin expression in CF.
To evaluate the expression of beta defensin (HBD-1 and HBD-2) mRNA and the presence of inflammatory markers (percentage of neutrophils and IL-8 mRNA expression) in CF and non-CF nasal mucosa.
Case-control study. Nasal brushing samples were obtained from 22 stable adult CF patients and 32 non-CF controls (25 healthy individuals and 7 individuals with acute cold). Samples were subjected to analysis involving mRNA expression (semiquantitative RT-PCR) and differential cell counting.
Defensins and inflammatory markers were expressed at low levels in healthy individuals and at high levels in subjects with acute cold. In non-CF controls, defensin expression correlated significantly with inflammatory parameters (p < 0.001). In CF, defensin mRNA expression was comparable to healthy individuals (p = 0.2). In contrast to non-CF controls, in CF patients high levels of inflammatory markers did not correlate with defensin mRNA levels.
Defensin expression is not upregulated in CF epithelium in response to inflammatory stimuli. Further studies are necessary to elucidate whether this is a consequence of the CF gene mutation.
防御素的缺乏或失活可能会促进囊性纤维化(CF)患者肺部的慢性细菌定植。CF鼻上皮表现出典型的生化异常,可用于研究CF中防御素的表达。
评估CF和非CF鼻黏膜中β防御素(HBD-1和HBD-2)mRNA的表达以及炎症标志物的存在情况(中性粒细胞百分比和IL-8 mRNA表达)。
病例对照研究。从22名病情稳定的成年CF患者和32名非CF对照者(25名健康个体和7名患急性感冒的个体)获取鼻拭子样本。对样本进行mRNA表达分析(半定量逆转录聚合酶链反应)和细胞分类计数。
防御素和炎症标志物在健康个体中表达水平较低,在患急性感冒的个体中表达水平较高。在非CF对照者中,防御素表达与炎症参数显著相关(p < 0.001)。在CF患者中,防御素mRNA表达与健康个体相当(p = 0.2)。与非CF对照者不同,CF患者中高水平的炎症标志物与防御素mRNA水平不相关。
CF上皮中的防御素表达不会因炎症刺激而上调。有必要进一步研究这是否是CF基因突变的结果。