Abstract

Allele-level resolution data at primary HLA typing is the ideal for most histocompatibility testing laboratories. Many high-throughput molecular HLA typing approaches are unable to determine the phase of observed DNA sequence polymorphisms, leading to ambiguous results. The use of higher resolution methods is often restricted due to cost and time limitations. Here we report on the feasibility of using Pacific Biosciences’ Single Molecule Real-Time (SMRT) DNA sequencing technology for high-resolution and high-throughput HLA typing. Seven DNA samples were typed for HLA-A, -B and -C. The results showed that SMRT DNA sequencing technology was able to generate sequences that spanned entire HLA Class I genes that allowed for accurate allele calling. Eight novel genomic HLA class I sequences were identified, four were novel alleles, three were confirmed as genomic sequence extensions and one corrected an existing genomic reference sequence. This method has the potential to revolutionize the field of HLA typing. The clinical impact of achieving this level of resolution HLA typing data is likely to considerable, particularly in applications such as organ and blood stem cell transplantation where matching donors and recipients for their HLA is of utmost importance.

Highlights

  • The HLA genes are located within one of the most gene rich regions of the human genome, the Major Histocompatibility Complex (MHC), on the short arm of chromosome 6 (6p21.3)

  • The MHC is divided into three distinct regions referred to as class I, II and III, with the HLA genes being located within the class I and class II regions

  • These consent forms are in accordance with the Human Tissue Authority (HTA) UK, European Federation for Immunogenetics (EFI), and Clinical Pathology Accreditation (CPA) regulatory body guidelines

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Summary

Introduction

The HLA genes are located within one of the most gene rich regions of the human genome, the Major Histocompatibility Complex (MHC), on the short arm of chromosome 6 (6p21.3). Many of these genes, including HLA, encode proteins that have a critical role in immune responses[1, 2]. The MHC is divided into three distinct regions referred to as class I, II and III, with the HLA genes being located within the class I and class II regions. Over 12,200 HLA alleles have been identified to date (December 2014), with in excess of 9,200 being variants of the HLA class I genes alone [www.ebi.ac.uk/imgt/hla] [4, 5]

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