SYNLAB MVZ Augsburg GmbH, Gubener Straße 39, 86156, Augsburg, Germany.
Eur J Clin Microbiol Infect Dis. 2019 Mar;38(3):529-539. doi: 10.1007/s10096-018-03455-1. Epub 2019 Feb 4.
Case-control study for the evaluation of innovative test formats for second-tier testing for the serodiagnosis of Lyme borreliosis (LB). A head-to-head comparison was performed with the test systems ViraStripe, SeraSpot, ViraChip, and recomBead. Serum samples from 62 patients (21 erythema migrans, 33 Lyme neuroborreliosis, 8 late LB) and 91 controls (including 29 potentially cross-reacting sera) were tested. For ViraChip and recomBead, optimised interpretation criteria were developed for both IgG and IgM. The most important modification for the proposed interpretation criteria for ViraChip is the interpretation of strong (> 2.5-fold above cutoff) singular IgG reactions against VlsE as positive. This significantly improves sensitivity (32 to 85%, p < 0.0001) without significant changes in specificity (borderline reactions interpreted as negative). By application of our modified rules, specificity of ViraChip IgM is significantly increased (89 to 97%, p < 0.05; borderline results included to negatives), and sensitivities of recomBead IgG and IgM are also significantly improved (69 to 87%, p < 0.01, and 57 to 74%, p < 0.01, respectively; borderline results included to positives). Further improvement of sensitivity by the rating of strong singular IgG reactions against VlsE as positive can also be shown for recomBead. IgG/IgM result combinations must be interpreted as a function of the assumed disease stage, and the best combinations differ for the various assays. Application of our proposed interpretation criteria significantly improve the discriminatory abilities of two assays; however, this must be confirmed with other data sets. Recommendations from Scientific Societies should be updated as may be necessary.
用于评价莱姆病(LB)血清学二级检测创新检测方法的病例对照研究。对 ViraStripe、SeraSpot、ViraChip 和 recomBead 检测系统进行了头对头比较。检测了 62 例患者(21 例游走性红斑、33 例莱姆神经Borreliosis、8 例晚期 LB)和 91 例对照(包括 29 例可能的交叉反应血清)的血清样本。针对 ViraChip 和 recomBead,为 IgG 和 IgM 分别开发了优化的解释标准。对于 ViraChip 建议的解释标准最重要的修改是,将针对 VlsE 的强烈(高于临界值 2.5 倍以上)单一 IgG 反应解释为阳性。这显著提高了敏感性(32%至 85%,p<0.0001),特异性无明显变化(边界反应解释为阴性)。应用我们的修改规则,ViraChip IgM 的特异性显著提高(89%至 97%,p<0.05;将边界结果包括为阴性),recomBead IgG 和 IgM 的敏感性也显著提高(69%至 87%,p<0.01;57%至 74%,p<0.01;将边界结果包括为阳性)。还可以显示,将针对 VlsE 的强烈单一 IgG 反应评为阳性也可以进一步提高 recomBead 的敏感性。IgG/IgM 结果组合必须根据假定的疾病阶段进行解释,并且不同检测方法的最佳组合也不同。应用我们建议的解释标准可显著提高两种检测方法的鉴别能力;然而,这需要用其他数据集进行验证。有必要时,科学学会的建议应进行更新。