Molecular determinant-based typing of KIR alleles and KIR ligands

Copyright © 2010 Elsevier Inc. All rights reserved.

Détails bibliographiques
Publié dans:Clinical immunology (Orlando, Fla.). - 1999. - 138(2011), 3 vom: 03. März, Seite 274-81
Auteur principal: Bari, Rafijul (Auteur)
Autres auteurs: Leung, Matthias, Turner, Victoria E, Embrey, Christy, Rooney, Barbara, Holladay, Martha, Leung, Wing
Format: Article en ligne
Langue:English
Publié: 2011
Accès à la collection:Clinical immunology (Orlando, Fla.)
Sujets:Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't HLA-A Antigens HLA-B Antigens HLA-C Antigens KIR2DL1 protein, human Ligands Receptors, KIR2DL1
Description
Résumé:Copyright © 2010 Elsevier Inc. All rights reserved.
Killer cell immunoglobulin-like receptors (KIRs) regulate NK cell function. KIRs and their HLA ligands are highly polymorphic in nature with substantial allelic polymorphism. At present, there is a lack of an expedient method for KIR and HLA allele typing with relevant functional information. Here, we developed a single-nucleotide polymorphism (SNP) assay to type various allele groups of KIR2DL1 with distinct functional properties based on polymorphism at position 245. We also established a SNP assay to type different KIR ligands based on polymorphism at position 77 in HLA-C and position 83 in HLA-B and -A. Our SNP assays for KIR and KIR ligand typing are much cheaper and faster than existing high-resolution typing. Importantly, our high-throughput methods provide readouts that are informative in predicting NK cell activity in health, disease, and transplantation
Description:Date Completed 14.04.2011
Date Revised 20.10.2021
published: Print-Electronic
Citation Status MEDLINE
ISSN:1521-7035
DOI:10.1016/j.clim.2010.12.002