Limits of the MAIPA assay when differentiating high-titered platelet-reactive antibodies.

A Agildere, D Wernet, M Schnaidt
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Abstract

Experience with the MAIPA assay for the diagnosis of platelet-reactive antibodies has shown that high-titered antibodies falsify the test results. We here demonstrate 2 cases: i) A serum with high-titered HLA antibodies (100% panel reactivity in the LCT, titer between 4,000 and 12,000), and ii) Serum with a high-titered anti-HPA-1a (titer in the MAIPA assay 1,000). In both cases, it can be demonstrated that these antibodies led to unspecific reactions. In the 1st case, they interfered with the diagnosis of additional platelet-specific antibodies. Only the use of HLA-compatible platelets allowed a correct identification. On the other hand, in the high-titered anti-HPA-1a unspecific reactions were seen with the glycoproteins Ib/IX, Ia/IIa, and beta 2-microglobulin, leading to misinterpretations. These examples demonstrate that, in the test conditions as described, a correct diagnosis of high-titered sera might only be achieved by using compatible HLA or HPA cells.

MAIPA法鉴别高滴度血小板反应性抗体的局限性。
MAIPA检测诊断血小板反应性抗体的经验表明,高滴度抗体会伪造检测结果。我们在这里展示了2例:i)高滴度HLA抗体血清(LCT中100%的整体反应性,滴度在4000到12000之间),ii)高滴度抗hpa -1a血清(MAIPA测定滴度为1000)。在这两种情况下,可以证明这些抗体导致非特异性反应。在第一个病例中,他们干扰了额外的血小板特异性抗体的诊断。只有使用hla相容的血小板才能进行正确的鉴定。另一方面,在高滴度的抗hpa -1a中,与糖蛋白Ib/IX, Ia/IIa和β 2微球蛋白发生非特异性反应,导致误解。这些例子表明,在上述测试条件下,高滴度血清的正确诊断可能只能通过使用兼容的HLA或HPA细胞来实现。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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