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杀伤细胞免疫球蛋白样受体(KIR)基因多样性研究:KIR2DL2、KIR2DL5和KIR2DS5

Investigation of killer cell immunoglobulin-like receptor (KIR) gene diversity: KIR2DL2, KIR2DL5 and KIR2DS5.

作者信息

Gonzalez A, Meenagh A, Sleator C, Middleton D

机构信息

Northern Ireland Regional Histocompatibility and Immunogenetics Laboratory, City Hospital, Belfast, UK.

出版信息

Tissue Antigens. 2008 Jul;72(1):11-20. doi: 10.1111/j.1399-0039.2008.01050.x. Epub 2008 May 20.

Abstract

Human killer cell immunoglobulin-like receptor (KIR) genes are important for restraining natural killer cytotoxicity toward cells with autologous human leukocyte antigen (HLA) while targeting cells lacking or expressing low levels of self-HLA molecules. KIR gene content and alleles vary across individual genomes and populations, requiring specialized laboratory tools for their characterization. Here, we detail methods based on sequence-specific polymerase chain reaction amplification and oligonucleotide probe hybridization to identify alleles of KIR2DL2, KIR2DL5A, KIR2DL5B and KIR2DS5. Allele frequencies for a Northern Irish population of 354 individuals typed with this system are given, along with results from 132 cell lines from the International Histocompatibility Workshop that cover many world populations. This information complements published reports by our laboratory for allele-level typing of other KIR members, totaling 12 of the 17 known genes. These methods are allowing us to characterize KIR haplotypes in our population.

摘要

人类杀伤细胞免疫球蛋白样受体(KIR)基因对于抑制自然杀伤细胞对具有自体人类白细胞抗原(HLA)的细胞的细胞毒性,同时靶向缺乏或表达低水平自身HLA分子的细胞非常重要。KIR基因含量和等位基因在个体基因组和群体中各不相同,需要专门的实验室工具来对其进行表征。在这里,我们详细介绍基于序列特异性聚合酶链反应扩增和寡核苷酸探针杂交的方法,以鉴定KIR2DL2、KIR2DL5A、KIR2DL5B和KIR2DS5的等位基因。给出了使用该系统分型的354名北爱尔兰人群的等位基因频率,以及来自国际组织相容性研讨会的132个细胞系的结果,这些细胞系涵盖了许多世界人群。这些信息补充了我们实验室发表的关于其他KIR成员等位基因水平分型的报告,已知的17个基因中共有12个。这些方法使我们能够对我们群体中的KIR单倍型进行表征。

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