Emory University, Department of Pathology and Laboratory Medicine, Atlanta, GA, USA.
Emory University, Department of Pathology and Laboratory Medicine, Atlanta, GA, USA.
Hum Immunol. 2020 Dec;81(12):663-670. doi: 10.1016/j.humimm.2020.09.002. Epub 2020 Oct 6.
Though solid-phase single antigen bead (SAB) testing has provided major advances to the HLA community and organ allocation, it has not been without limitations. In particular, false-positive reactions lead to interpretative challenges and the potential to preclude a transplant if the corresponding antigens are deemed unacceptable. Two different vendor platforms are commercially available for SAB testing, one more recent than the other. The aim herein was to assess the benefit of using the newer SAB platform in situations where the primary platform yielded suspicious (specifically, false positive) reactions. Therefore, 42 serum samples with commonly encountered false-positive patterns observed in our laboratory were tested with the newer platform. Cases were classified as resolved, equivalent, or divergent based on whether the second platform produced no reactivity, the same pattern, or a distinctly different pattern compared to the primary platform, respectively. Approximately 33% of cases were resolved, 46% were equivalent, and 21% were divergent. The project revealed advantages of adding a second SAB platform to the laboratory's test menu including resolving challenging samples and including broader coverage of different alleles and unique class II alpha/beta subunit combinations. However, the challenges of validating, maintaining, and billing for another test method in the laboratory may be barriers to routine use.
虽然固相单抗原珠 (SAB) 检测为 HLA 社区和器官分配带来了重大进展,但它并非没有局限性。特别是,假阳性反应导致解释上的挑战,并有可能排除移植,如果相应的抗原被认为不可接受。目前有两种不同的供应商平台可用于 SAB 检测,一种比另一种更新。本研究旨在评估在主要平台产生可疑(特别是假阳性)反应的情况下使用更新的 SAB 平台的益处。因此,我们使用更新的平台检测了 42 份在我们实验室中常见的具有假阳性模式的血清样本。根据第二个平台是否产生无反应、相同的模式或与主要平台明显不同的模式,将病例分别分类为解决、等效或发散。大约 33%的病例得到解决,46%的病例等效,21%的病例发散。该项目揭示了在实验室测试菜单中添加第二个 SAB 平台的优势,包括解决具有挑战性的样本以及涵盖更广泛的不同等位基因和独特的 II 类 alpha/beta 亚单位组合。然而,验证、维护和计费另一种实验室测试方法的挑战可能成为常规使用的障碍。