Bernard Nicole F
Research Institute of the McGill University Health Centre (RI-MUHC), Montreal, QC, Canada.
Division of Experimental Medicine, McGill University, Montreal, QC, Canada.
AIDS Res Ther. 2017 Sep 12;14(1):38. doi: 10.1186/s12981-017-0172-9.
The anti-HIV activity of natural killer (NK) cells could be induced fast enough to potentially prevent the establishment of HIV infection. Epidemiological studies identified two genotypes encoding NK receptors that contribute to NK cell function, that were more frequent in people who remained uninfected despite multiple HIV exposures than in HIV-susceptible subjects. NK cells from carriers of the *h/y+B57 genotype have higher NK cell functional potential and inhibit HIV replication in autologous HIV-infected CD4+ T cells (iCD4) more potently than those from carriers of non-protective genotypes. HIV suppression depends on the secretion of CC-chemokines that block HIV entry into CD4+ cells. NK cell education and the effect of HIV infection on iCD4 cell surface expression of MHC-I antigens both influenced NK cell responses to autologous iCD4. The second KIR3DS1 homozygous protective genotype encodes an activating receptor that upon interacting with its HLA-F ligand on iCD4 induces anti-viral activity.
自然杀伤(NK)细胞的抗HIV活性能够被快速诱导,从而有可能预防HIV感染的建立。流行病学研究确定了两种编码NK受体的基因型,这些基因型有助于NK细胞发挥功能,在尽管多次接触HIV仍未感染的人群中比在易感染HIV的受试者中更为常见。与非保护性基因型携带者相比,h/y+B57基因型携带者的NK细胞具有更高的功能潜力,并且能更有效地抑制自体HIV感染的CD4+T细胞(iCD4)中的HIV复制。HIV抑制取决于CC趋化因子的分泌,这些趋化因子可阻止HIV进入CD4+细胞。NK细胞的成熟以及HIV感染对iCD4细胞表面MHC-I抗原表达的影响,均会影响NK细胞对自体iCD4的反应。第二种KIR3DS1纯合保护性基因型编码一种激活受体,该受体与iCD4上的HLA-F配体相互作用时会诱导抗病毒活性。