Frequency of human platelet antigens (HPA) in the Greek population as deduced from the first registry of HPA-typed blood donors.

IF 1.8 4区 医学 Q3 HEMATOLOGY Vox Sanguinis Pub Date : 2024-09-23 DOI:10.1111/vox.13739
Georgios Kaltsounis, Evangelia Boulomiti, Dimitroula Papadopoulou, Dimitrios Stoimenis, Fotios Girtovitis, Eleni Hasapopoulou-Matamis
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Abstract

Background and objectives: Human platelet antigens (HPA) play a central role in foetal and neonatal alloimmune thrombocytopenia (FNAIT), post-transfusion purpura and some cases of platelet therapy refractoriness. The frequency distribution of HPA had not been studied in the Greek population before we started to create a registry of HPA-typed apheresis platelet donors. The aim of this study was the determination of the frequency of various HPA in the Greek population, through the establishment of a registry of typed donors.

Materials and methods: Here, we report on the first 1000 platelet donors of Greek origin who gave informed consent and were genotyped for 12 pairs of antithetical HPA by Single Specific Primer-Polymerase Chain Reaction (SSP-PCR), including HPA-1, HPA-3, HPA-5 and HPA-15. Antigen frequencies are reported, and allele frequencies were calculated and compared with other European and non-European populations. Tested donors cover all ABO and Rhesus D antigen spectrum.

Results: Antigen and allele frequencies are very similar to other White populations. The frequency of HPA-1bb is 2.9% in our study, and the frequency of HPA-2b, HPA-4b, HPA-9b and HPA-15b is also slightly higher than in other literature reports, while the frequency of HPA-15b was found higher than that of HPA-15a.

Conclusion: We report antigen and allele frequencies for a large array of clinically significant HPA for the first time in the Greek population. Frequencies are consistent with other European populations. This registry of HPA-typed platelet donors, available to donate on demand, is an important asset for the treatment of FNAIT cases in Greece.

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从首个 HPA 型献血者登记处推断出的希腊人口中人类血小板抗原 (HPA) 的频率。
背景和目的:人类血小板抗原(HPA)在胎儿和新生儿同种免疫性血小板减少症(FNAIT)、输血后紫癜和某些血小板治疗难治性病例中起着核心作用。在我们开始建立 HPA 型无细胞血小板捐献者登记册之前,尚未对希腊人群中 HPA 的频率分布进行研究。本研究的目的是通过建立分型捐献者登记册,确定各种 HPA 在希腊人群中的频率。材料和方法:在此,我们报告了首批 1000 名希腊裔血小板捐献者的情况,他们在知情同意的情况下,通过单特异性引物聚合酶链反应(SSP-PCR)对 12 对反义 HPA 进行了基因分型,包括 HPA-1、HPA-3、HPA-5 和 HPA-15。报告了抗原频率,计算了等位基因频率,并与其他欧洲和非欧洲人群进行了比较。接受测试的供体涵盖所有 ABO 和恒河猴 D 抗原谱:抗原频率和等位基因频率与其他白种人非常相似。在我们的研究中,HPA-1bb 的频率为 2.9%,HPA-2b、HPA-4b、HPA-9b 和 HPA-15b 的频率也略高于其他文献报道,而 HPA-15b 的频率高于 HPA-15a:我们首次报告了希腊人群中大量具有临床意义的 HPA 的抗原和等位基因频率。频率与其他欧洲人群一致。这个可按需捐献的 HPA 型血小板捐献者登记册是希腊治疗 FNAIT 病例的重要资产。
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来源期刊
Vox Sanguinis
Vox Sanguinis 医学-血液学
CiteScore
4.40
自引率
11.10%
发文量
156
审稿时长
6-12 weeks
期刊介绍: Vox Sanguinis reports on important, novel developments in transfusion medicine. Original papers, reviews and international fora are published on all aspects of blood transfusion and tissue transplantation, comprising five main sections: 1) Transfusion - Transmitted Disease and its Prevention: Identification and epidemiology of infectious agents transmissible by blood; Bacterial contamination of blood components; Donor recruitment and selection methods; Pathogen inactivation. 2) Blood Component Collection and Production: Blood collection methods and devices (including apheresis); Plasma fractionation techniques and plasma derivatives; Preparation of labile blood components; Inventory management; Hematopoietic progenitor cell collection and storage; Collection and storage of tissues; Quality management and good manufacturing practice; Automation and information technology. 3) Transfusion Medicine and New Therapies: Transfusion thresholds and audits; Haemovigilance; Clinical trials regarding appropriate haemotherapy; Non-infectious adverse affects of transfusion; Therapeutic apheresis; Support of transplant patients; Gene therapy and immunotherapy. 4) Immunohaematology and Immunogenetics: Autoimmunity in haematology; Alloimmunity of blood; Pre-transfusion testing; Immunodiagnostics; Immunobiology; Complement in immunohaematology; Blood typing reagents; Genetic markers of blood cells and serum proteins: polymorphisms and function; Genetic markers and disease; Parentage testing and forensic immunohaematology. 5) Cellular Therapy: Cell-based therapies; Stem cell sources; Stem cell processing and storage; Stem cell products; Stem cell plasticity; Regenerative medicine with cells; Cellular immunotherapy; Molecular therapy; Gene therapy.
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