Petit N Y, Baillou C, Burlion A, Dorgham K, Levacher B, Amiel C, Schneider V, Lemoine F M, Gorochov G, Marodon G
Sorbonne Universités, UPMC Univ PARIS 06, CR7, INSERM U1135, CNRS, Centre d'Immunologie et des Maladies Infectieuses (CIMI), Paris, France.
Sorbonne Universités, UPMC Univ PARIS 06, CR7, INSERM U959, Paris, France.
Gene Ther. 2016 Feb;23(2):144-50. doi: 10.1038/gt.2015.101. Epub 2015 Oct 21.
Targeting viral entry is the most likely gene therapy strategy to succeed in protecting the immune system from pathogenic HIV-1 infection. Here, we evaluated the efficacy of a gene transfer lentiviral vector expressing a combination of viral entry inhibitors, the C46 peptide (an inhibitor of viral fusion) and the P2-CCL5 intrakine (a modulator of CCR5 expression), to prevent CD4⁺ T-cell infection in vivo. For this, we used two different models of HIV-1-infected mice, one in which ex vivo genetically modified human T cells were grafted into immunodeficient NOD.SCID.γc⁻/⁻mice before infection and one in which genetically modified T cells were derived from CD34⁺ hematopoietic progenitors grafted few days after birth. Expression of the transgenes conferred a major selective advantage to genetically modified CD4⁺ T cells, the frequency of which could increase from 10 to 90% in the blood following HIV-1 infection. Moreover, these cells resisted HIV-1-induced depletion, contrary to non-modified cells that were depleted in the same mice. Finally, we report lower normalized viral loads in mice having received genetically modified progenitors. Altogether, our study documents that targeting viral entry in vivo is a promising avenue for the future of HIV-1 gene therapy in humans.
靶向病毒进入是最有可能成功保护免疫系统免受致病性HIV-1感染的基因治疗策略。在此,我们评估了一种表达病毒进入抑制剂组合(C46肽,一种病毒融合抑制剂;P2-CCL5内趋化因子,一种CCR5表达调节剂)的基因转移慢病毒载体在体内预防CD4⁺T细胞感染的疗效。为此,我们使用了两种不同的HIV-1感染小鼠模型,一种是在感染前将体外基因改造的人T细胞移植到免疫缺陷的NOD.SCID.γc⁻/⁻小鼠体内,另一种是基因改造的T细胞来源于出生几天后移植的CD34⁺造血祖细胞。转基因的表达赋予了基因改造的CD4⁺T细胞主要的选择性优势,在HIV-1感染后,其在血液中的频率可从10%增加到90%。此外,与在同一只小鼠中被耗尽的未修饰细胞相反,这些细胞抵抗HIV-1诱导的耗竭。最后,我们报告在接受基因改造祖细胞的小鼠中,标准化病毒载量较低。总之,我们的研究证明,在体内靶向病毒进入是未来人类HIV-1基因治疗的一个有前景的途径。