Embers Monica E, Hasenkampf Nicole R, Barnes Mary B, Didier Elizabeth S, Philipp Mario T, Tardo Amanda C
Division of Bacteriology & Parasitology Tulane National Primate Research Center, Tulane University Health Sciences Center, Covington, Louisiana, USA
Division of Bacteriology & Parasitology Tulane National Primate Research Center, Tulane University Health Sciences Center, Covington, Louisiana, USA.
Clin Vaccine Immunol. 2016 Apr 4;23(4):294-303. doi: 10.1128/CVI.00685-15. Print 2016 Apr.
The systematically difficult task of diagnosing Lyme disease can be simplified by sensitive and specific laboratory tests. The currently recommended two-tier test for serology is highly specific but falls short in sensitivity, especially in the early acute phase. We previously examined serially collected serum samples from Borrelia burgdorferi-infected rhesus macaques and defined a combination of antigens that could be utilized for detection of infection at all phases of disease in humans. The five B. burgdorferi antigens, consisting of OspC, OspA, DbpA, OppA2, and the C6 peptide, were combined into a fluorescent cytometric bead-based assay for the detection of B. burgdorferi antigen-specific IgG antibodies. Samples from Lyme disease patients and controls were used to determine the diagnostic value of this assay. Using this sample set, we found that our five-antigen multiplex IgG assay exhibited higher sensitivity (79.5%) than the enzyme immunoassay (EIA) (76.1%), the two-tier test (61.4%), and the C6 peptide enzyme-linked immunosorbent assay (ELISA) (77.2%) while maintaining specificity over 90%. When detection of IgM was added to the bead-based assay, the sensitivity improved to 91%, but at a cost of reduced specificity (78%). These results indicate that the rational combination of antigens in our multiplex assay may offer an improved serodiagnostic test for Lyme disease.
灵敏且特异的实验室检测能够简化莱姆病诊断这项系统性难题。目前推荐的血清学两层检测法特异性很高,但灵敏度不足,尤其是在疾病的早期急性期。我们之前连续检测了感染伯氏疏螺旋体的恒河猴的血清样本,并确定了一组抗原组合,可用于检测人类疾病各阶段的感染情况。这五种伯氏疏螺旋体抗原,即外膜蛋白C(OspC)、外膜蛋白A(OspA)、结合蛋白A(DbpA)、寡肽转运蛋白A2(OppA2)和C6肽,被组合成一种基于荧光细胞计数微球的检测方法,用于检测伯氏疏螺旋体抗原特异性IgG抗体。利用莱姆病患者和对照的样本确定该检测方法的诊断价值。通过这套样本,我们发现我们的五抗原多重IgG检测法的灵敏度(79.5%)高于酶免疫测定(EIA)(76.1%)、两层检测法(61.4%)和C6肽酶联免疫吸附测定(ELISA)(77.2%),同时保持特异性超过90%。当在基于微球的检测中加入IgM检测时,灵敏度提高到91%,但特异性有所降低(78%)。这些结果表明,我们多重检测法中抗原的合理组合可能为莱姆病提供一种改进的血清学诊断检测方法。