Transplant Immunology Laboratory, Royal Liverpool and Broadgreen University Hospital and School of Infection and Host Defence, Liverpool University, Liverpool, UK.
Immunology. 2010 Jan;129(1):8-19. doi: 10.1111/j.1365-2567.2009.03208.x.
The functions of human natural killer (NK) cells are controlled by diverse families of antigen receptors. Prominent among these are the killer cell immunoglobulin-like receptors (KIR), a family of genes clustered in one of the most variable regions of the human genome. Within this review we discuss the vast polymorphism of the KIR gene complex which rivals that of the human leucocyte antigen (HLA) complex. There are several aspects to this polymorphism. Initially there is presence/absence of individual KIR genes, with four of these genes, termed framework genes, being present in all individuals tested to date, except on those very occasional instances when the gene has been deleted. Within each gene, alleles are present at different frequencies. We provide details of a new website that enables convenient searching for data on KIR gene, allele and genotype frequencies in different populations and show how these frequencies vary in different worldwide populations and the high probability of individuals differing in their KIR repertoire when both gene and allele polymorphism is considered. The KIR genes present in an individual may be classified into A and/or B haplotypes, which respectively have a more inhibitory role or a more activating role on the function of the NK cell. Family studies have been used to ascertain the make-up of these haplotypes, inclusion of allele typing enabling determination of whether one or two copies of a particular gene is present. In addition to genetic diversification the KIR gene complex shows differences at the functional level with different alleles having different protein expression levels and different avidity with their HLA ligand.
人类自然杀伤 (NK) 细胞的功能受多种抗原受体家族的控制。其中突出的是杀伤细胞免疫球蛋白样受体 (KIR),这是一个基因家族,聚集在人类基因组最易变的区域之一。在这篇综述中,我们讨论了 KIR 基因复合物的巨大多态性,其与人类白细胞抗原 (HLA) 复合物相媲美。这种多态性有几个方面。首先是个体 KIR 基因的存在/缺失,其中有 4 个基因,称为框架基因,目前在所有已测试的个体中都存在,除非基因已经缺失。在每个基因中,等位基因以不同的频率存在。我们提供了一个新网站的详细信息,该网站可方便地搜索不同人群中 KIR 基因、等位基因和基因型频率的数据,并展示了这些频率在不同世界人群中的变化,以及当同时考虑基因和等位基因多态性时,个体在其 KIR 库中存在差异的高概率。个体中存在的 KIR 基因可分为 A 和/或 B 单倍型,它们分别对 NK 细胞的功能具有更抑制性或更激活作用。家族研究已被用于确定这些单倍型的组成,包括等位基因分型,以确定是否存在一个或两个特定基因的副本。除了遗传多样化之外,KIR 基因复合物在功能水平上也存在差异,不同的等位基因具有不同的蛋白表达水平和与 HLA 配体的不同亲和力。