杀伤细胞免疫球蛋白样受体(KIR)基因及其在乌干达人群中的 HLA-C 配体。

Killer cell immunoglobulin-like receptor (KIR) genes and their HLA-C ligands in a Ugandan population.

机构信息

Department of Obstetrics and Gynecology, Makerere University, Kampala, Uganda.

出版信息

Immunogenetics. 2013 Nov;65(11):765-75. doi: 10.1007/s00251-013-0724-7. Epub 2013 Aug 24.

Abstract

Killer cell immunoglobulin-like receptor (KIR) genes are expressed by natural killer cells and encoded by a family of genes exhibiting considerable haplotypic and allelic variation. HLA-C molecules, the dominant ligands for KIR, are present in all individuals and are discriminated by two KIR epitopes, C1 and C2. We studied the frequencies of KIR genes and HLA-C1 and C2 groups in a large cohort (n = 492) from Kampala, Uganda, East Africa and compared our findings with published data from other populations in sub-Saharan Africa (SSA) and several European populations. We find considerably more KIR diversity and weaker linkage disequilibrium in SSA compared to the European populations and describe several novel KIR genotypes. C1 and C2 frequencies were similar to other SSA populations with a higher frequency of the C2 epitope (54.9 %) compared to Europe (average 39.7 %). Analysis of this large cohort from Uganda in the context of other African populations reveals variations in KIR and HLA-C1 and C2 that are consistent with migrations within Africa and potential selection pressures on these genes. Our results will help understand how KIR/HLA-C interactions contribute to resistance to pathogens and reproductive success.

摘要

杀伤细胞免疫球蛋白样受体 (KIR) 基因由自然杀伤细胞表达,由具有显著单倍型和等位基因变异性的基因家族编码。HLA-C 分子是 KIR 的主要配体,存在于所有个体中,并通过两个 KIR 表位 C1 和 C2 来区分。我们研究了来自东非坎帕拉的一个大型队列(n=492)的 KIR 基因和 HLA-C1 和 C2 组的频率,并将我们的发现与来自撒哈拉以南非洲(SSA)和几个欧洲人群的已发表数据进行了比较。与欧洲人群相比,我们在 SSA 中发现了更多的 KIR 多样性和较弱的连锁不平衡,并描述了几种新的 KIR 基因型。C1 和 C2 的频率与其他 SSA 人群相似,但 C2 表位的频率较高(54.9%),而欧洲的平均频率为 39.7%。在其他非洲人群的背景下对来自乌干达的这个大型队列进行分析,揭示了 KIR 和 HLA-C1 和 C2 的变化,这些变化与非洲内部的迁徙以及对这些基因的潜在选择压力一致。我们的研究结果将有助于了解 KIR/HLA-C 相互作用如何有助于抵抗病原体和生殖成功。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ad20/3824577/398096998357/251_2013_724_Fig1_HTML.jpg

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