| Literature DB >> 31558329 |
Medhat Askar1, Abeer Madbouly2, Leah Zhrebker3, Amanda Willis3, Shawna Kennedy3, Karin Padros4, Maria Beatriz Rodriguez4, Christian Bach5, Bernd Spriewald5, Reem Ameen6, Salem Al Shemmari6, Katerina Tarassi7, Alexandra Tsirogianni7, Nayera Hamdy8, Ghada Mossallam8, Gideon Hönger9, Regina Spinnler10, Gottfried Fischer11, Ingrid Fae11, Ronald Charlton12, Arthur Dunk13, Tamara A Vayntrub14, Michael Halagan2, Kazutoyo Osoegawa14, Marcelo Fernández-Viña15.
Abstract
Since their inception, the International HLA & Immunogenetics Workshops (IHIW) served as a collaborative platform for exchange of specimens, reference materials, experiences and best practices. In this report we present a subset of the results of human leukocyte antigen (HLA) haplotypes in families tested by next generation sequencing (NGS) under the 17th IHIW. We characterized 961 haplotypes in 921 subjects belonging to 250 families from 8 countries (Argentina, Austria, Egypt, Jamaica, Germany, Greece, Kuwait, and Switzerland). These samples were tested in a single core laboratory in a high throughput fashion using 6 different reagents/software platforms. Families tested included patients evaluated clinically as transplant recipients (kidney and hematopoietic cell transplant) and their respective family members. We identified 486 HLA alleles at the following loci HLA-A, -B, -C, -DRB1, -DRB3, -DRB4, -DRB5, -DQA1, -DQB1, -DPA1, -DPB1 (77, 115, 68, 69, 10, 6, 4, 44, 31, 20 and 42 alleles, respectively). We also identified nine novel alleles with polymorphisms in coding regions. This approach of testing samples from multiple laboratories across the world in different stages of technology implementation in a single core laboratory may be useful for future international workshops. Although data presented may not be reflective of allele and haplotype frequencies in the countries to which the families belong, they represent an extensive collection of 3rd and 4th field resolution level 11-locus haplotype associations of 486 alleles identified in families from 8 countries.Entities:
Keywords: Family; HLA haplotype; Linkage disequilibrium
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Year: 2019 PMID: 31558329 DOI: 10.1016/j.humimm.2019.07.298
Source DB: PubMed Journal: Hum Immunol ISSN: 0198-8859 Impact factor: 2.850