Fritzler Marvin J, Fritzler Mark L
Department of Medicine, Faculty of Medicine, University of Calgary, 3330 Hospital Drive NW, Calgary, Alberta, Canada.
Curr Med Chem. 2006;13(21):2503-12. doi: 10.2174/092986706778201639.
In the last decade, there has been a rapid proliferation of new technologies that are capable of identifying an increasing spectrum of autoantibodies and other biomarkers in autoimmune diseases. These newer diagnostic technologies include line immunoassays, addressable laser bead immunoassays, microarrays in microfluidics platforms and nanobarcode particles. Multiplexed bead assays are a particularly robust platform because they are adaptable to the detection of a variety of disease specific biomarkers, such as autoantibodies, cytokines, adipokines, drugs, oligonucleotides and single nucleotide polymorphisms, Although many laboratories have adopted a variety of these diagnostic platforms to improve turn around times and meet budget constraints, there is an urgent need to ensure that the rapid adoption of new technologies is attended by an appropriate balance of assay sensitivity and specificity.
在过去十年中,能够识别自身免疫性疾病中越来越多的自身抗体和其他生物标志物的新技术迅速涌现。这些更新的诊断技术包括线性免疫测定、可寻址激光珠免疫测定、微流控平台中的微阵列和纳米条形码颗粒。多重珠测定是一个特别强大的平台,因为它们适用于检测各种疾病特异性生物标志物,如自身抗体、细胞因子、脂肪因子、药物、寡核苷酸和单核苷酸多态性。尽管许多实验室已经采用了多种这些诊断平台来缩短周转时间并满足预算限制,但迫切需要确保在快速采用新技术的同时,适当平衡检测的灵敏度和特异性。