Human Leukocyte Antigen-A, B, C, DRB1, and DQB1 Allele and Haplotype Frequencies in a Subset of 237 Donors in the South African Bone Marrow Registry

Author:

Tshabalala Mqondisi1ORCID,Ingram Charlotte2,Schlaphoff Terry23,Borrill Veronica23,Christoffels Alan4,Pepper Michael S.1ORCID

Affiliation:

1. Department of Immunology, SAMRC Extramural Unit for Stem Cell Research and Therapy, Institute for Cellular and Molecular Medicine, Faculty of Health Sciences, University of Pretoria, Pretoria, South Africa

2. South African Bone Marrow Registry (SABMR), P.O. Box 13353 Mowbray, Cape Town 7705, South Africa

3. Laboratory for Tissue Immunology, National Health Laboratory Service, Groote Schuur Hospital, C21 Anzio Street, Observatory, Cape Town 7925, South Africa

4. SA MRC Bioinformatics Unit, South African National Bioinformatics Institute, University of Western Cape, Robert Sobukwe Road, Bellville, Cape Town 7535, South Africa

Abstract

Human leukocyte antigen- (HLA-) A, HLA-B, HLA-C, HLA-DRB1, and HLA-DQB1 allele and haplotype frequencies were studied in a subset of 237 volunteer bone marrow donors registered at the South African Bone Marrow Registry (SABMR). Hapl-o-Mat software was used to compute allele and haplotype frequencies from individuals typed at various resolutions, with some alleles in multiple allele code (MAC) format. Four hundred and thirty-eight HLA-A, 235 HLA-B, 234 HLA-DRB1, 41 HLA-DQB1, and 29 HLA-C alleles are reported. The most frequent alleles were A02:02g (0.096), B07:02g (0.082), C07:02g (0.180), DQB106:02 (0.157), and DRB115:01 (0.072). The most common haplotype was A03:01g~B07:02g~C07:02g~DQB106:02~DRB115:01 (0.067), which has also been reported in other populations. Deviations from Hardy-Weinberg equilibrium were observed in A, B, and DRB1 loci, with C~DQB1 being the only locus pair in linkage disequilibrium. This study describes allele and haplotype frequencies from a subset of donors registered at SABMR, the only active bone marrow donor registry in Africa. Although the sample size was small, our results form a key resource for future population studies, disease association studies, and donor recruitment strategies.

Funder

National Research Foundation

Publisher

Hindawi Limited

Subject

Immunology,General Medicine,Immunology and Allergy

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