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首页> 外文期刊>BMC Infectious Diseases >Quantitative investigation of factors relevant to the T cell spot test for tuberculosis infection in active tuberculosis
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Quantitative investigation of factors relevant to the T cell spot test for tuberculosis infection in active tuberculosis

机译:定量调查有关结核病患者结核病感染T细胞斑点试验的因素

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摘要

Previous qualitative studies suggested that the false negative rate of the T cell spot test for tuberculosis infection (T-SPOT.TB) is associated with many risk factors in tuberculosis patients. However, more precise quantitative studies are lacking. The purpose of this study was to investigate the factors affecting quantified spot-forming cells (SFCs) to early secreted antigenic target 6?kDa (ESAT-6) or culture filtrate protein 10?kDa (CFP-10) in patients with active tuberculosis. We retrospectively analyzed the data of 360 patients who met the inclusion criteria. Using the SFCs to ESAT-6 or CFP-10 levels as dependent variables, variables with statistical significance in the univariate analysis were subjected to optimal scaling regression analysis. The combination of ESAT-6 and CFP-10 (i.e., T-SPOT.TB) was analyzed by the exact logistic regression model. The results showed that the SFCs to ESAT-6 regression model had statistical significance (P??0.001) and that previous treatment and CD4+ and platelet counts were its independent risk factors (all P??0.05). Their importance levels were 0.095, 0.596 and 0.100, respectively, with a total of 0.791. The SFCs to CFP-10 regression model also had statistical significance (P??0.001); platelet distribution width and alpha-2 globulin were its independent risk factors (all P??0.05). Their importance levels were 0.287 and 0.247, respectively, with a total of 0.534. The quantification graph showed that quantified SFCs to ESAT-6 or CFP-10 grading had a linear correlation with risk factors. Albumin-globulin ratio, CD4+ and CD8+ were independent risk factors for false negative T-SPOT.TB (all P??0.05). In T-SPOT.TB-assisted diagnosis of patients with active tuberculosis, previous treatment, decreased CD4+ and platelet count might lead to the decreased SFCs to ESAT-6, decreased alpha-2 globulin and high platelet distribution width might lead to the decreased SFCs to CFP-10, decreased albumin-globulin ratio, CD4+ and CD8+ might lead to an increase in the false negative rate of the T-SPOT.TB.
机译:以前的定性研究表明,结核病感染的T细胞点测试(T-Spot.tb)的假阴性率与结核病患者的许多风险因素有关。然而,缺乏更精确的定量研究。本研究的目的是研究影响定量的点状细胞(SFC)至早期分泌的抗原靶6?KDA(ESAT-6)或培养滤液蛋白10的因素在有源结核病患者中KDA(CFP-10)。我们回顾性地分析了符合纳入标准的360名患者的数据。使用SFC作为ESAT-6或CFP-10级别作为依赖变量,对单变量分析中具有统计显着性的变量进行了最佳的缩放回归分析。通过确切的逻辑回归模型分析ESAT-6和CFP-10(即T-Spot.tb)的组合。结果表明,SFC对ESAT-6回归模型的统计学意义(P?<0.001),其先前的治疗和CD4 +和血小板计数是其独立的危险因素(所有P?<?0.05)。它们的重要性水平分别为0.095,0.596和0.100,共为0.791。 CFP-10回归模型的SFC也具有统计学意义(P?<0.001);血小板分布宽度和α-2球蛋白是其独立的危险因素(所有P?<?0.05)。它们的重要性水平分别为0.287和0.247,总共0.534。定量图表表明,定量的SFC与ESAT-6或CFP-10等级具有与风险因素的线性相关性。白蛋白 - 球蛋白比率,CD4 +和CD8 +是假阴性T-Spot的独立危险因素.Tb(所有P?<β05)。在T-Spot.TB辅助诊断患有活性结核病患者的诊断,先前治疗,降低CD4 +和血小板计数可能导致SFC减少到ESAT-6,降低α-2球蛋白和高血小板分布宽度可能导致SFC减少对于CFP-10,白蛋白 - 球蛋白比例降低,CD4 +和CD8 +可能导致T-Spot.tb的假负速率增加。

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