Identification of the rs9277534 HLA-DP expression marker by next generation sequencing for the selection of unrelated donors for hematopoietic cell transplantation.
3' Untranslated Regions
/ genetics
Alleles
Databases, Genetic
Exons
/ genetics
Genetic Loci
/ genetics
Genotype
Graft vs Host Disease
/ genetics
HLA-DP beta-Chains
/ genetics
Hematopoietic Stem Cell Transplantation
/ methods
High-Throughput Nucleotide Sequencing
Histocompatibility Testing
Humans
Polymorphism, Single Nucleotide
/ genetics
Unrelated Donors
HLA-DPB1 expression marker
NGS
SNP rs9277534
Journal
Human immunology
ISSN: 1879-1166
Titre abrégé: Hum Immunol
Pays: United States
ID NLM: 8010936
Informations de publication
Date de publication:
Oct 2019
Oct 2019
Historique:
received:
11
03
2019
revised:
10
05
2019
accepted:
23
05
2019
pubmed:
10
6
2019
medline:
27
2
2020
entrez:
10
6
2019
Statut:
ppublish
Résumé
Mismatching of an unrelated donor against a high-expression HLA-DPB1 recipient allele is associated with a high risk of graft-versus-host disease and mortality. The Seattle Cancer Care Alliance (SCCA) and Fred Hutchinson Cancer Research Center transplant program employs an algorithm to match for HLA-A, B, C, DRB1, DQB1 and DPB1 alleles (12/12) and to avoid, whenever possible, donor mismatching against a recipient high-expression HLA-DPB1 allele. HLA-DPB1 expression is associated with the rs9277534 A/G polymorphism located in the 3'UTR of the HLA-DPB1 gene. Next generation sequencing of HLA-DPB1 using the Illumina TruSight HLA V2 Sequencing Panel and Conexio Assign software analyses provides information on rs9277534 variants without the need for any additional SNP testing. Here we present the molecular location of rs9277534 in NGS data and discuss the challenges to resolve HLA-DPB1 ambiguities.
Identifiants
pubmed: 31176504
pii: S0198-8859(19)30273-3
doi: 10.1016/j.humimm.2019.05.010
pii:
doi:
Substances chimiques
3' Untranslated Regions
0
HLA-DP beta-Chains
0
HLA-DPB1 antigen
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
828-833Informations de copyright
Copyright © 2019 American Society for Histocompatibility and Immunogenetics. Published by Elsevier Inc. All rights reserved.