Division of Clinical Immunology, Research Institute of the McGill University Health Centre, McGill University, Canada.
J Immunol. 2010 Feb 15;184(4):2057-64. doi: 10.4049/jimmunol.0902621. Epub 2010 Jan 8.
Epidemiological studies in humans have implicated carriage of combinations of genes encoding certain KIR3DL1 (killer Ig-like receptor 3DL1) alleles and their HLA-Bw4 ligands in slower progression to AIDS, lower viral load and protection from infection. Given that the KIR3DL1*h/y/HLA-B57 genetic combination is strongly associated with favorable HIV outcomes, we measured responses from NK cells isolated from these individuals by multiparametric flow cytometry for cytokine secretion and degranulation in response to stimulation with HLA-devoid cells to assess whether the KIR/HLA compound genotypes linked to better HIV outcome favor increased NK cell functional potential. Our results indicate that NK cells from these individuals had increased functional potential, particularly in the KIR3DL1(+) NK cell subset. These results support a link between KIR/HLA genotypes and NK cell function and could provide an explanation for the observation that some KIR/HLA combinations are associated protective phenotypes in the context of host-HIV interactions.
在人类的流行病学研究中,携带某些编码杀伤免疫球蛋白样受体 3DL1(KIR3DL1)等位基因及其 HLA-Bw4 配体的基因组合与艾滋病进展缓慢、病毒载量降低和免受感染有关。鉴于 KIR3DL1*h/y/HLA-B57 遗传组合与良好的 HIV 结果密切相关,我们通过多参数流式细胞术测量了从这些个体中分离出的 NK 细胞对 HLA 缺失细胞刺激的反应,以评估与更好的 HIV 结果相关的 KIR/HLA 复合基因型是否有利于增加 NK 细胞的功能潜力。我们的结果表明,这些个体的 NK 细胞具有更高的功能潜力,特别是在 KIR3DL1(+) NK 细胞亚群中。这些结果支持 KIR/HLA 基因型与 NK 细胞功能之间的联系,并可能为观察到某些 KIR/HLA 组合在宿主-HIV 相互作用中与保护性表型相关提供解释。