Grifoni Alba, Montesano Carla, Colizzi Vittorio, Amicosante Massimo
Alba Grifoni, Carla Montesano, Vittorio Colizzi, Department of Biology, University of Rome "Tor Vergata", 00100 Rome, Italy.
World J Virol. 2015 May 12;4(2):124-33. doi: 10.5501/wjv.v4.i2.124.
Host and viral factors deeply influence the human immunodeficiency virus (HIV) disease progression. Among them human leukocyte antigen (HLA) locus plays a key role at different levels. In fact, genes of the HLA locus have shown the peculiar capability to modulate both innate and adaptive immune responses. In particular, HLA class I molecules are recognized by CD8(+) T-cells and natural killers (NK) cells towards the interaction with T cell receptor (TCR) and Killer Immunoglobulin Receptor (KIR) 3DL1 respectively. Polymorphisms within the different HLA alleles generate structural changes in HLA class I peptide-binding pockets. Amino acid changes in the peptide-binding pocket lead to the presentation of a different set of peptides to T and NK cells. This review summarizes the role of HLA in HIV progression toward acquired immunodeficiency disease syndrome and its receptors. Recently, many studies have been focused on determining the HLA binding-peptides. The novel use of immune-informatics tools, from the prediction of the HLA-bound peptides to the modification of the HLA-receptor complexes, is considered. A better knowledge of HLA peptide presentation and recognition are allowing new strategies for immune response manipulation to be applied against HIV virus.
宿主和病毒因素对人类免疫缺陷病毒(HIV)疾病进展有深刻影响。其中,人类白细胞抗原(HLA)基因座在不同层面发挥关键作用。事实上,HLA基因座的基因已显示出调节先天性和适应性免疫反应的独特能力。特别是,HLA I类分子分别被CD8(+) T细胞和自然杀伤(NK)细胞识别,以分别与T细胞受体(TCR)和杀伤细胞免疫球蛋白受体(KIR)3DL1相互作用。不同HLA等位基因内的多态性会导致HLA I类肽结合口袋发生结构变化。肽结合口袋中的氨基酸变化会导致向T细胞和NK细胞呈递不同的肽组。本综述总结了HLA在HIV向获得性免疫缺陷综合征进展过程中的作用及其受体。最近,许多研究都集中在确定HLA结合肽上。考虑了免疫信息学工具的新用途,从预测HLA结合肽到修饰HLA-受体复合物。对HLA肽呈递和识别的更好了解使得针对HIV病毒的免疫反应操纵新策略得以应用。