Seo D H, Park S S, Kim D W, Furihata K, Ueno I, Han K S
Department of Clinical Pathology, Seoul National University College of Medicine, Korea.
Transfus Med. 1998 Jun;8(2):129-32. doi: 10.1046/j.1365-3148.1998.00138.x.
Human platelet-specific antigens (HPAs) are found on platelet membrane glycoproteins and are the target of platelet alloantibodies that mediate platelet destruction in neonatal alloimmune thrombocytopenia (NAIT), post-transfusion purpura (PTP) and refractoriness to platelet transfusion therapy. The biallelic polymorphism of all HPA systems is known to be due to a substitution of a single base pair. This study was performed to investigate the frequency of the HPA genes in Koreans, based on these substitutions. The genotypes of eight HPA systems were determined by polymerase chain reaction using sequence-specific primers (PCR-SSP) for HPA-1, -2, -4, -5, and -8 and restriction fragment length polymorphism (RFLP) for HPA-3, -6, and -7. The gene frequencies obtained from 200 unrelated Koreans were 0.99 and 0.01 for HPA-1a and -1b, 0.92 and 0.08 for HPA-2a and -2b, 0.55 and 0.45 for HPA-3a and -3b, 0.99 and 0.01 for HPA-4a and -4b, 0.98 and 0.02 for HPA-5a and -5b, and 0.98 and 0.02 for HPA-6a and -6b. All the individuals tested were homozygotes for HPA-7a and HPA-8a. It has been reported that the HPA-1b antigen is extremely rare (less than 0.3%) in Oriental populations, but this study suggests that the frequency of this antigen in Koreans (2.0%) is higher than in Japanese and Chinese populations.
人类血小板特异性抗原(HPAs)存在于血小板膜糖蛋白上,是血小板同种抗体的作用靶点,这些抗体在新生儿同种免疫性血小板减少症(NAIT)、输血后紫癜(PTP)以及血小板输血治疗无效中介导血小板破坏。已知所有HPA系统的双等位基因多态性是由于单个碱基对的替换。基于这些替换,本研究旨在调查韩国人中HPA基因的频率。使用针对HPA-1、-2、-4、-5和-8的序列特异性引物聚合酶链反应(PCR-SSP)以及针对HPA-3、-6和-7的限制性片段长度多态性(RFLP)来确定八个HPA系统的基因型。从200名无亲缘关系的韩国人获得的基因频率为:HPA-1a和-1b分别为0.99和0.01,HPA-2a和-2b分别为0.92和0.08,HPA-3a和-3b分别为0.55和0.45,HPA-4a和-4b分别为0.99和0.01,HPA-5a和-5b分别为0.98和0.02,HPA-6a和-6b分别为0.98和0.02。所有检测个体均为HPA-7a和HPA-8a的纯合子。据报道,HPA-1b抗原在东方人群中极为罕见(低于0.3%),但本研究表明该抗原在韩国人中的频率(2.0%)高于日本人和中国人。