Goujon C, Jarrosson-Wuillème L, Bernaud J, Rigal D, Darlix J-L, Cimarelli A
INSERM U412, Ecole Normale Supérieure de Lyon, IFR 128 BioSciences Lyon-Gerland, Lyon, France.
Gene Ther. 2006 Jun;13(12):991-4. doi: 10.1038/sj.gt.3302753. Epub 2006 Mar 9.
Modification of dendritic cells (DCs) is a promising avenue for gene therapy purposes, given the versatility and the multiplicity of functions of these cells. In this study, we show that preincubation of monocyte-derived DCs with low amounts of non-infectious virion-like particles derived from the simian immunodeficiency virus (SIV(MAC) VLPs) increases up to 10-fold the efficiency of transduction by HIV-1 lentiviral vectors at low multiplicity of infections yielding up to 90% of transduced cells, in the absence of alterations of DCs behavior. This effect is restricted to DCs and specified by the viral accessory protein Vpx. Thus, preincubation with empty VLPs of SIV(MAC) can be used in transduction protocols to increase the efficacy of HIV-1-mediated modification of DCs.
鉴于树突状细胞(DCs)功能的多样性,对其进行改造是基因治疗的一个有前景的途径。在本研究中,我们发现,用低量源自猴免疫缺陷病毒(SIV(MAC))的非感染性病毒样颗粒(VLPs)对单核细胞衍生的DCs进行预孵育,在低感染复数下可将HIV-1慢病毒载体的转导效率提高至10倍,产生高达90%的转导细胞,且不会改变DCs的行为。这种效应仅限于DCs,并且由病毒辅助蛋白Vpx决定。因此,用SIV(MAC)的空VLPs进行预孵育可用于转导方案,以提高HIV-1介导的DCs改造的效率。