Author/Authors :
Bari، نويسنده , , Rafijul and Leung، نويسنده , , Matthias and Turner، نويسنده , , Victoria E. and Embrey، نويسنده , , Christy and Rooney، نويسنده , , Barbara and Holladay، نويسنده , , Martha and Leung، نويسنده , , Wing، نويسنده ,
Abstract :
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.
Keywords :
Killer cell immunoglobulin-like receptor , Human leukocyte antigen , Natural Killer cell , Single-nucleotide polymorphism