智利血型的种族多样性:对北部、南部和中部地区抗原的基因型、表型、等位基因和免疫潜能的综合分析。

IF 1.8 4区 医学 Q3 HEMATOLOGY Vox Sanguinis Pub Date : 2024-10-16 DOI:10.1111/vox.13746
María Antonieta Núñez Ahumada, Fernando Pontigo Gonzalez, Carlos Arancibia Aros, Andrea Canals, Lilian Jara Soza, Valeska Rodriguez, Catalina Vargas, Edgardo Saa, Lilian Castilho
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引用次数: 0

摘要

背景和目的:关于智利人口血型的现有信息来自于对原住民群体的研究和常规血清学检测结果。本研究的目的是利用分子方法对智利北部、中部和南部献血者的基因型、表型和血型等位基因进行全面分析:对来自智利北部、中部和南部献血者的 850 份样本进行了基因分型。计算并比较了不同地区的等位基因、基因型和抗原频率。对其中 602 份样本进行了血凝分析,并调查了表型与基因型之间的差异。利用圣地亚哥供体的抗原频率和同一地区患者的同种异体抗体频率,通过吉布利特方程计算出抗原的免疫原性:结果:发现了低流行率等位基因、变异等位基因和导致高流行率抗原缺失的等位基因。三个地区的抗原频率存在显著差异。血清学结果与分子结果之间的差异主要归因于影响抗原表达的分子背景。在计算抗原的免疫原性时,Dia 抗原的数值最高:这些研究结果首次对智利人的血型抗原进行了分子鉴定。我们的研究结果突出表明,有必要使用分子工具来探索变异表型、低频抗原和缺乏特异性抗血清的抗原(血凝法无法检测)背后的基因型。此外,这些研究还强调了了解血型在不同人群中分布情况的重要性。
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Ethnic diversity in Chilean blood groups: A comprehensive analysis of genotypes, phenotypes, alleles and the immunogenic potential of antigens in northern, southern and central regions.

Background and objectives: The available information on blood groups in the Chilean population is derived from studies on aboriginal cohorts and routine serological test results. The purpose of this study is to conduct a comprehensive analysis of genotypes, phenotypes and blood group alleles in donors from northern, central and southern Chile using molecular methods.

Materials and methods: Overall, 850 samples from donors in northern, central and southern Chile were genotyped. Allelic, genotypic and antigenic frequencies were calculated and compared among regions. Of these, 602 samples were analysed by haemagglutination, and discrepancies found between phenotypes and genotypes were investigated. The immunogenic potential of antigens was calculated by the Giblett equation, using the antigenic frequencies of donors from Santiago and the alloantibody frequencies of patients from the same region.

Results: Alleles of low prevalence, variant alleles and those responsible for the absence of high-prevalence antigens were found. Significant differences were observed between the antigenic frequencies of the three regions. Discrepancies between serologic and molecular results were mostly attributed to the molecular background affecting antigen expression. In the calculation of the immunogenic potential of antigens, the highest value was attributed to the Dia antigen.

Conclusion: These findings represent the first molecular characterization of blood group antigens in Chileans. Our results highlight the necessity of using molecular tools to explore the genotypes underlying variant phenotypes, low-frequency antigens and antigens lacking specific antisera that cannot be detected by haemagglutination. Additionally, they emphasize the importance of understanding the distribution of blood groups among different populations.

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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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