Molecular determinant-based typing of KIR alleles and KIR ligands

被引:21
作者
Bari, Rafijul [1 ]
Leung, Matthias [1 ]
Turner, Victoria E. [2 ]
Embrey, Christy [2 ]
Rooney, Barbara [1 ]
Holladay, Martha [1 ]
Leung, Wing [1 ,3 ]
机构
[1] St Jude Childrens Hosp, Dept Oncol, Memphis, TN 38105 USA
[2] St Jude Childrens Hosp, Dept Pathol, Memphis, TN 38105 USA
[3] Univ Tennessee, Ctr Hlth Sci, Dept Pediat, Memphis, TN 38163 USA
关键词
Natural killer cell; Killer cell immunoglobulin-like receptor; Human leukocyte antigen; Single-nucleotide polymorphism; NATURAL-KILLER-CELLS; MHC CLASS-I; NK CELLS; HLA-C; RECEPTOR; CANCER; ALLOREACTIVITY; POLYMORPHISMS; INHIBITION; EXPRESSION;
D O I
10.1016/j.clim.2010.12.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
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. (C) 2010 Elsevier Inc. All rights reserved.
引用
收藏
页码:274 / 281
页数:8
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