TY - JOUR
T1 - HLA Haplotypes In 250 Families
T2 - The Baylor Laboratory Results And A Perspective On A Core NGS Testing Model For The 17th International HLA And Immunogenetics Workshop
AU - Askar, Medhat
AU - Madbouly, Abeer
AU - Zhrebker, Leah
AU - Willis, Amanda
AU - Kennedy, Shawna
AU - Padros, Karin
AU - Rodriguez, Maria Beatriz
AU - Bach, Christian
AU - Spriewald, Bernd
AU - Ameen, Reem
AU - Shemmari, Salem Al
AU - Tarassi, Katerina
AU - Tsirogianni, Alexandra
AU - Hamdy, Nayera
AU - Mossallam, Ghada
AU - Hönger, Gideon
AU - Spinnler, Regina
AU - Fischer, Gottfried
AU - Fae, Ingrid
AU - Charlton, Ronald
AU - Dunk, Arthur
AU - Vayntrub, Tamara A.
AU - Halagan, Michael
AU - Osoegawa, Kazutoyo
AU - Fernández-Viña, Marcelo
N1 - Publisher Copyright:
© 2019 American Society for Histocompatibility and Immunogenetics
PY - 2019/11
Y1 - 2019/11
N2 - 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.
AB - 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.
KW - Family
KW - HLA haplotype
KW - Linkage disequilibrium
UR - https://www.scopus.com/pages/publications/85072519916
U2 - 10.1016/j.humimm.2019.07.298
DO - 10.1016/j.humimm.2019.07.298
M3 - Article
C2 - 31558329
AN - SCOPUS:85072519916
SN - 0198-8859
VL - 80
SP - 897
EP - 905
JO - Human Immunology
JF - Human Immunology
IS - 11
ER -