Abstract

The HLA-B15 typing by serological approaches defined the serological subgroups (or splits) B62, B63, B75, B76, B77 and B70 (B71 and B72). The scarcity of sera with specific anti-HLA antibodies makes the serological typing method difficult to discriminate a high variety of HLA antigens, especially between the B15 antigen subgroups. Advancements in DNA-based technologies have led to a switch from serological typing to high-resolution DNA typing methods. DNA sequencing techniques assign B15 specificity to all alleles in the HLA-B*15 allele group, without distinction of the serological split equivalents. However, the presence of antibodies in the patient defined as split B15 antigens urges the identification of HLA-B*15 allele subtypes of the donor, since the presence of donor-specific antibodies is an important contraindication for organ transplantation. Although the HLA dictionary comprises information regarding the serological subtypes of HLA alleles, there are currently 394 B15 antigens out of 516 in the IPD-IMGT/HLA database (3.38.0) without any assigned serological subtype. In this regard, we aimed to identify specific amino acid patterns for each B*15 serological split, in order to facilitate the assignment of B*15 alleles to serological equivalents after high-resolution molecular typing. As a result, serological specificities of 372/394 not yet assigned alleles could be predicted based on amino acid motifs. Furthermore, two new serological types were identified and added, B62-Bw4 and B71-Bw4.

Highlights

  • Serological typing has been used for a long time to determine HLA typing of patients and donors

  • HLA-B15 antigens HLA-B15 antigens included in the analysis have been obtained from the IPD-IMGT/HLA database regarding each B*15 alleles (B*15) allele that differs in the second field as a different antigen and excluding the null and questionable alleles

  • We provide a straightforward approach to predict serological splits of HLA-B*15 alleles based on amino acid polymorphisms

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Summary

Introduction

Serological typing has been used for a long time to determine HLA typing of patients and donors. This method is based on complement-dependent cytotoxicity (CDC) test or microlymphocytotoxicity assay, which measures the reactivity of a panel of sera containing well-characterized anti-HLA antibodies (Terasaki and McClelland 1964). When an antibody against a B15 split antigen in the serum of the recipient is detected, the serological subtype of the B15 antigen present on the donor cells must be identified in order to determine whether this anti-B15 antibody is donor-specific. Without knowing the B15 serological equivalent, the risk of rejection for patients having anti-B15split HLA antibodies is present and all B*15 typed donors are considered contra-indicated for transplantation for this patient

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