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

Author:

Ho Quan Yao12ORCID,Phang Chew Yen3,Liew Ian Tatt12ORCID,Lai May Ling3,Tien Carolyn Shan‐Yeu12ORCID,Thangaraju Sobhana12ORCID,Chan Marieta3,Kee Terence12ORCID

Affiliation:

1. Department of Renal Medicine Singapore General Hospital Singapore Singapore

2. SingHealth Duke‐NUS Transplant Centre Singapore Singapore

3. Blood Services Group Health Sciences Authority Singapore Singapore

Abstract

AbstractHuman 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.

Publisher

Wiley

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine,Immunology

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