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机构地区:[1]北京解放军第309医院全军结核病研究所,全军结核病防治重点实验室,100091
出 处:《临床肺科杂志》2015年第2期195-198,共4页Journal of Clinical Pulmonary Medicine
基 金:国家自然科学基金资助(No 81071318)
摘 要:目的通过测定外周血单个核细胞(PBMCs)中单核细胞趋化蛋白(MCP-1)的表达水平,探讨其对结核诊断的意义。方法收集活动性肺结核患者、结核潜伏感染(latent tuberculosis infection,LTBI)及非结核感染健康对照个体的全血并提取PBMCs,经结核特异性抗原肽刺激后,采用基因芯片分析方法和酶联免疫吸附试验(ELISA)比较各组MCP-1表达情况。结果基因芯片分析发现活动期肺结核患者MCP-1表达(4460±3154)明显高于LTBI组(951.8±641.5,P=0.0043)。ELISA分析结果发现刺激前三组MCP-1浓度无差异(P=0.4747),而刺激后只有活动期肺结核患者组(37112±3790 pg/ml)和非结核感染健康对照组(15546±3143 pg/ml)之间的MCP-1浓度相比有显著差异(P<0.0001)。结论高表达的MCP-1有可能作为诊断结核及监测结核严重程度的指标之一,但是无法区分潜伏感染和活动期感染病例。Objective To evaluate the diagnostic value of MCP-1 for tuberculosis by assaying its expression level in PBMCs.Methods The peripheral blood was collected from pulmonary tuberculosis patients,latent tubercu-losis infection (LTBI)and non-tuberculosis infection healthy individuals.Then MCP-1 level in PBMCs stimulated with Mtb-specific antigens was detected using microarray analysis methods and enzyme-linked immunosorbent assay (ELISA).Results Microarray analysis showed that MCP-1 level in patients with active tuberculosis (4460 ±31 54) was significantly higher than that in the LTBI group (951.8 ±641.5,P=0.0043).ELISA analysis revealed no difference in MCP-1 concentration in PBMCs culture supernatants among the three groups before stimulation (P=0.4747),but there was significant difference in MCP-1 concentration between the active tuberculosis patients group (371 1 2 ±3790 pg/ml)and the healthy control group (1 5546 ±31 43 pg/ml)after stimulation (P〈0.0001 ).Con-clusion The high expression of MCP-1 can be used as an indicator for diagnosis of tuberculosis and monitor the dis-ease severity,but it can't distinguish latent infection from active infection.
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