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疑似胎儿/新生儿同种免疫性血小板减少症中母体血小板同种抗体和自身抗体的频率,重点关注人类血小板抗原-15同种免疫

Frequencies of maternal platelet alloantibodies and autoantibodies in suspected fetal/neonatal alloimmune thrombocytopenia, with emphasis on human platelet antigen-15 alloimmunization.

作者信息

Mandelbaum M, Koren D, Eichelberger B, Auerbach L, Panzer S

机构信息

Clinic for Blood Group Serology, Medical University Vienna, Vienna, Austria.

出版信息

Vox Sang. 2005 Jul;89(1):39-43. doi: 10.1111/j.1423-0410.2005.00662.x.

Abstract

BACKGROUND AND OBJECTIVES

Serological evaluation of maternal sera for platelet antibodies in suspected fetal/neonatal alloimmune thrombocytopenia (FNAITP) discloses in only approximately 30% of individuals a platelet-specific antibody. Transfusion-induced alloimmunization against human platelet antigen-15 (HPA-15) has been reported to be about as common as against HPA-5, the second most common platelet antibody. Thus, anti-HPA-15 may also contribute significantly to yet-unclear cases of FNAITP.

MATERIALS AND METHODS

In this retrospective analysis, we provide data on maternal platelet antibodies from 309 mothers who delivered an offspring with suspected FNAITP.

RESULTS

Genotyping maternal and paternal samples (together n = 573) revealed a gene frequency of 0.496 for HPA-15a and a gene frequency of 0.504 for HPA-15b. HPA-15 antibodies were detected in 2% of all samples. Anti-HPA-15a and -15b were detected in two and three samples, respectively. One serum reacted equally with HPA-15a and -15b platelets. The most frequent platelet-specific antibodies were anti-HPA-1a (22%), but anti-HPA-5b (8.4%) were more frequent than anti-HPA-15. In addition, panreactive (5.5%) or autoreactive (5.2%) anti-GPIIb/IIIa or anti-GPIb/IX were detectable in maternal samples.

CONCLUSIONS

These data indicate that HPA-15 alloimmunization needs only to be considered in subjects with suspected FNAITP if no other platelet-specific antibody is detectable. The presence of panreactive or autoreactive antibodies should also be considered in neonatal thrombocytopenia.

摘要

背景与目的

对疑似胎儿/新生儿同种免疫性血小板减少症(FNAITP)孕妇血清进行血小板抗体的血清学评估,仅在约30%的个体中发现血小板特异性抗体。据报道,输血诱导的针对人类血小板抗原-15(HPA-15)的同种免疫与针对第二常见血小板抗体HPA-5的同种免疫发生率相当。因此,抗HPA-15也可能在不明原因的FNAITP病例中起重要作用。

材料与方法

在这项回顾性分析中,我们提供了309名分娩疑似FNAITP后代母亲的血小板抗体数据。

结果

对母亲和父亲样本(共573份)进行基因分型,结果显示HPA-15a的基因频率为0.496,HPA-15b的基因频率为0.504。在所有样本中,2%检测到HPA-15抗体。分别在两份和三份样本中检测到抗HPA-15a和-15b。一份血清与HPA-15a和-15b血小板的反应相同。最常见的血小板特异性抗体是抗HPA-1a(22%),但抗HPA-5b(8.4%)比抗HPA-15更常见。此外,在母亲样本中可检测到泛反应性(5.5%)或自身反应性(5.2%)抗糖蛋白IIb/IIIa或抗糖蛋白Ib/IX。

结论

这些数据表明,只有在未检测到其他血小板特异性抗体的疑似FNAITP患者中,才需要考虑HPA-15同种免疫。新生儿血小板减少症也应考虑泛反应性或自身反应性抗体的存在。

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