Wieser C, Stumpf D, Grillhösl C, Lengenfelder D, Gay S, Fleckenstein B, Ensser A
Institut für Klinische und Molekulare Virologie, Universität Erlangen-Nürnberg, Erlangen, Germany.
Gene Ther. 2005 Mar;12(5):395-406. doi: 10.1038/sj.gt.3302424.
Herpesviral saimiri-(HVS) mediated expression of bovine growth hormone was one of the first applications of an episomal viral vector for gene therapy. Meanwhile, the long-term persistence of HVS vectors has been confirmed in a broad spectrum of infectable target cells in vitro and in vivo. Regulated gene expression is useful for many applications of gene therapy. Therefore, we inserted the Mifepristone-antiprogestin-inducible expression system (GeneSwitchtrade mark) into HVS viral vectors to regulate the combined expression of anti-inflammatory cytokines, IL-10 and IL-1RA. Constitutive CMV-promoter/enhancer-driven and Mifepristone-inducible cytokine expression was compared in the viral context in transduced primary human fibroblasts and rheumatoid arthritis (RA) fibroblast-like cells (RASF). Long-term persistence of vector genomes was shown for both construct types. Constitutive expression was efficient and more rapid in onset than in the inducible system, in which the selective induction of interleukin expression along with low background levels was obtained by Mifepristone concentrations that were more than 1000-fold below those required for endogenous Progesterone antagonism. Furthermore, transgene expression corresponded to vector doses. Global patterns of cytokine secretion were not significantly changed due to viral transduction, indicating a rather inert behavior of the viral vector itself. In an attempt to emulate the inflammatory cytokine-enriched environment in rheumatoid arthritic joints, the function of the vectors could be demonstrated in vitro by the successful blockade of IL-1beta-stimulated matrix-metalloproteinase (MMP)-3 expression from RASF cells. Evaluation of this system in future studies, in suitable long-term SCID models of RA or in non-human primate models, will exploit the possible in vivo benefits of nontransforming HVS vectors in gene therapy.
疱疹病毒萨氏病毒(HVS)介导的牛生长激素表达是游离病毒载体用于基因治疗的首批应用之一。同时,HVS载体在体外和体内多种可感染靶细胞中的长期持久性已得到证实。调控基因表达对基因治疗的许多应用都很有用。因此,我们将米非司酮-抗孕激素诱导表达系统(GeneSwitch商标)插入HVS病毒载体,以调控抗炎细胞因子IL-10和IL-1RA的联合表达。在转导的原代人成纤维细胞和类风湿性关节炎(RA)成纤维样细胞(RASF)中,比较了组成型CMV启动子/增强子驱动的和米非司酮诱导的细胞因子表达。两种构建体类型的载体基因组均显示出长期持久性。组成型表达效率高且起效比诱导系统更快,在诱导系统中,通过米非司酮浓度获得白细胞介素表达的选择性诱导以及低背景水平,该浓度比内源性孕酮拮抗所需浓度低1000倍以上。此外,转基因表达与载体剂量相对应。由于病毒转导,细胞因子分泌的整体模式没有明显改变,表明病毒载体本身的行为相当惰性。为了模拟类风湿性关节炎关节中富含炎性细胞因子的环境,通过成功阻断RASF细胞中IL-1β刺激的基质金属蛋白酶(MMP)-3表达,可在体外证明载体的功能。在未来的研究中,在合适的RA长期SCID模型或非人类灵长类动物模型中对该系统进行评估,将利用非转化HVS载体在基因治疗中可能的体内益处。