Unrepresented human leucocyte antigen alleles in single-antigen bead assays: A single-centre cohort study

IF 2.3 4区 医学 Q3 GENETICS & HEREDITY
Quan Yao Ho, Chew Yen Phang, Ian Tatt Liew, May Ling Lai, Carolyn Shan-Yeu Tien, Sobhana Thangaraju, Marieta Chan, Terence Kee
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引用次数: 0

Abstract

Human leucocyte antigen (HLA) alleles may generate antibodies that are undetectable by routine single-antigen beads (SABs) assays if their unique epitopes are unrepresented. We aimed to describe the prevalence and explore the potential impact of unrepresented HLA alleles in standard SAB kits in our cohort. All individuals who had undergone two-field HLA typing (HLA-A/B/C/DRB1/DQA1/-DQB1/-DPA1/-DPB1) from February 2021 to July 2023 were included. Two-field HLA-DRB3/4/5 typing was imputed. Each unrepresented allele was compared with the most similar represented allele in the standard LABScreen, LABScreen ExPlex (One Lambda) and the LIFECODES (Immucor) SAB kits. Differences in eplet expression (HLA Eplet Registry) were identified. Differences in three-dimensional molecular structures were visualized using generated models (SWISS-MODEL). Two-field HLA typing was performed for 116 individuals. Overall, 16.7% of all HLA alleles, found in 36.2% of individuals, were unrepresented by all SAB test kits. Four eplets, found in 12.9% of individuals, were unrepresented in at least 1 SAB kit. Non-Chinese individuals were more likely to have unrepresented HLA alleles and eplets than Chinese individuals. There were differences in HLA allele and eplet representation amongst the different SAB test kits. Use of supplementary SAB test kits may improve HLA allele and eplet representation. Although some HLA alleles were unrepresented, most epitopes were represented in current SAB kits. However, some unrepresented alleles may contain epitopes which may generate undetectable antibodies. Further studies may be needed to investigate the potential clinical impact of these unrepresented alleles and eplets, especially in certain ethnic populations or at-risk individuals.

单抗原珠检测中未代表的人白细胞抗原等位基因:一项单中心队列研究
人类白细胞抗原(HLA)等位基因可能产生抗体,无法检测常规的单抗原珠(SABs)检测,如果其独特的表位是不代表。我们的目的是描述我们的队列中标准SAB试剂盒中未代表的HLA等位基因的患病率并探索其潜在影响。所有于2021年2月至2023年7月接受HLA双区分型(HLA- a /B/C/DRB1/DQA1/-DQB1/-DPA1/-DPB1)的个体均被纳入研究。输入双域HLA-DRB3/4/5分型。将每个未代表的等位基因与标准LABScreen、LABScreen ExPlex (One Lambda)和LIFECODES (Immucor) SAB试剂盒中最相似的代表等位基因进行比较。确定了eplet表达差异(HLA eplet Registry)。使用生成的模型(SWISS-MODEL)可视化三维分子结构的差异。对116例患者进行HLA双区分型。总体而言,在36.2%的个体中发现的16.7%的HLA等位基因未被所有SAB检测试剂盒所代表。在12.9%的个体中发现的四个小体在至少一个SAB试剂盒中没有代表。与中国人相比,非中国人更有可能具有未被代表的HLA等位基因和等位基因。不同的SAB检测试剂盒在HLA等位基因和等位基因的表达上存在差异。使用补充的SAB检测试剂盒可以改善HLA等位基因和等位基因的表达。虽然一些HLA等位基因未被代表,但大多数表位在目前的SAB试剂盒中都有代表。然而,一些未代表的等位基因可能含有可能产生无法检测到的抗体的表位。可能需要进一步的研究来调查这些未代表的等位基因和等位基因的潜在临床影响,特别是在某些种族人群或高危个体中。
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来源期刊
CiteScore
4.70
自引率
0.00%
发文量
48
审稿时长
6-12 weeks
期刊介绍: The International Journal of Immunogenetics (formerly European Journal of Immunogenetics) publishes original contributions on the genetic control of components of the immune system and their interactions in both humans and experimental animals. The term ''genetic'' is taken in its broadest sense to include studies at the evolutionary, molecular, chromosomal functional and population levels in both health and disease. Examples are: -studies of blood groups and other surface antigens- cell interactions and immune response- receptors, antibodies, complement components and cytokines- polymorphism- evolution of the organisation, control and function of immune system components- anthropology and disease associations- the genetics of immune-related disease: allergy, autoimmunity, immunodeficiency and other immune pathologies- All papers are seen by at least two independent referees and only papers of the highest quality are accepted.
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