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一种用于检测急性钩端螺旋体病血清抗钩端螺旋体脂多糖 IgM 的免疫层析检测法的研制与评价。

Development and evaluation of an immunochromatographic assay to detect serum anti-leptospiral lipopolysaccharide IgM in acute leptospirosis.

机构信息

Department of Pathobiology, Faculty of Science, Mahidol University, Bangkok, Thailand.

Thawangpha Hospital, Nan, Thailand.

出版信息

Sci Rep. 2017 May 23;7(1):2309. doi: 10.1038/s41598-017-02654-8.

Abstract

Leptospirosis is a common life-threatening disease worldwide. However, its diagnosis is frequently ineffective because the gold standard bacterial culture and microscopic agglutination test (MAT) are usually positive 1-2 weeks after the disease onset. We thus developed an immunochromatographic assay (LEPkit) to detect serum anti-leptospiral lipopolysaccharide (LPS) IgM for rapid diagnosis of acute leptospirosis. Using referenced sera of 77 leptospirosis and 91 non-leptospirosis cases, LEPkit yielded 97.4% sensitivity, 94.5% specificity, 93.8 positive predictive value (PPV), 97.7% negative predictive value (NPV), and 95.8% accuracy. The stability of this kit stored for up to 18 months and its reproducibility were confirmed. Testing in 74 new cases using samples at admission-phase and subsequent paired samples (total n = 135), overall sensitivity was 98.5%, whereas that of culture and single MAT (≥1:400) was 15.6% and 35.6%, respectively. When only the samples at admission-phase were used (n = 74), the sensitivity remained at 98.7%, whereas that of culture and single MAT (≥1:400) was 28.4% and 13.5%, respectively. In summary, our LEPkit was far more effective than any conventional methods for the diagnosis of acute leptospirosis, especially within the first few days after the disease onset. The ease of use, stability and reproducibility further enhance its feasibility for clinical use on-site.

摘要

钩端螺旋体病是一种全球性的常见危及生命的疾病。然而,由于金标准的细菌培养和显微镜凝集试验(MAT)通常在疾病发病后 1-2 周才呈阳性,因此其诊断常常无效。我们因此开发了一种免疫层析检测试剂盒(LEPkit),用于检测血清抗钩端螺旋体脂多糖(LPS)IgM,以快速诊断急性钩端螺旋体病。使用 77 份钩端螺旋体病和 91 份非钩端螺旋体病参考血清,LEPkit 的灵敏度为 97.4%,特异性为 94.5%,阳性预测值(PPV)为 93.8%,阴性预测值(NPV)为 97.7%,准确率为 95.8%。该试剂盒的稳定性在储存长达 18 个月后得到了确认,其重现性也得到了验证。在 74 例新发病例中,使用入院期样本和随后的配对样本(总 n=135)进行检测,总体灵敏度为 98.5%,而培养和单次 MAT(≥1:400)的灵敏度分别为 15.6%和 35.6%。当仅使用入院期样本(n=74)时,灵敏度仍保持在 98.7%,而培养和单次 MAT(≥1:400)的灵敏度分别为 28.4%和 13.5%。总之,我们的 LEPkit 比任何传统方法都更有效地诊断急性钩端螺旋体病,尤其是在疾病发病后的头几天。其易于使用、稳定性和重现性进一步增强了其在现场临床使用的可行性。

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