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Selected RD1 Peptides for Active Tuberculosis Diagnosis: Comparison of a Gamma Interferon Whole-Blood Enzyme-Linked Immunosorbent Assay and an Enzyme-Linked Immunospot Assay

机译:选定的RD1肽用于主动性肺结核诊断:γ干扰素全血酶联免疫吸附测定法和酶联免疫斑点测定法的比较

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We recently set up a gamma interferon (IFN-γ) enzyme-linked immunospot assay (ELISPOT), using selected early secreted antigenic target 6 (ESAT-6) peptides, that appears specific for active tuberculosis (A-TB). However, ELISPOT is difficult to automate. Thus, the objective of this study was to determine if the same selected peptides may be used in a technique more suitable for routine work in clinical laboratories, such as whole-blood enzyme-linked immunosorbent assay (WBE). For this purpose, 27 patients with A-TB and 41 control patients were enrolled. Our WBE, using the already described selected peptides from ESAT-6 plus three new ones from culture filtrate protein 10, was performed, and data were compared with those obtained by ELISPOT. Using our selected peptides, IFN-γ production, evaluated by both WBE and ELISPOT, was significantly higher in patients with A-TB than in controls (P < 0.0001). Statistical analysis showed a good correlation between the results obtained by WBE and ELISPOT (r = 0.80, P < 0.001). To substantiate our data, we compared our WBE results with those obtained by QuantiFERON-TB Gold, a whole-blood assay based on region of difference 1 (RD1) overlapping peptides approved for TB infection diagnosis. We observed a slightly higher sensitivity with QuantiFERON-TB Gold than with our WBE (89% versus 81%); however, our test provided a better specificity result (90% versus 68%). In conclusion, results obtained by WBE based on selected RD1 peptides significantly correlate with those generated by ELISPOT. Moreover, our assay appears more specific for A-TB diagnosis than QuantiFERON-TB Gold, and thus it may represent a complementary tool for A-TB diagnosis for routine use in clinical laboratories.
机译:我们最近使用选定的早期分泌性抗原靶标6(ESAT-6)肽建立了伽玛干扰素(IFN-γ)酶联免疫斑点测定(ELISPOT),该肽对活动性肺结核(A-TB)具特异性。但是,ELISPOT很难实现自动化。因此,本研究的目的是确定是否可以将相同选择的肽用于更适合临床实验室常规工作的技术,例如全血酶联免疫吸附测定(WBE)。为此,招募了27例A-TB患者和41例对照患者。使用已经描述过的ESAT-6选定的肽加上培养滤液蛋白10中的三个新肽进行了我们的WBE,并将数据与ELISPOT获得的数据进行了比较。使用我们选择的肽,通过WBE和ELISPOT评估的A-TB患者的IFN-γ产生显着高于对照组( P <0.0001)。统计分析表明,WBE与ELISPOT获得的结果之间具有良好的相关性( r = 0.80, P <0.001)。为了证实我们的数据,我们将WBE结果与QuantiFERON-TB Gold获得的结果进行了比较,QuantiFERON-TB Gold是基于被批准用于TB感染诊断的差异1(RD1)重叠肽区域的全血检测方法。我们发现QuantiFERON-TB Gold的敏感性比WBE略高(89%比81%);但是,我们的测试提供了更好的特异性结果(90%比68%)。总之,WBE基于选定的RD1肽获得的结果与ELISPOT产生的结果显着相关。此外,我们的检测方法似乎比QuantiFERON-TB Gold更能特异性地诊断A-TB,因此它可能代表临床实验室常规使用的A-TB诊断的补充工具。

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