Porada Christopher D, Park Paul J, Tellez Joe, Ozturk Ferhat, Glimp Hudson A, Almeida-Porada Graça, Zanjani Esmail D
Department of Animal Biotechnology, University of Nevada at Reno, 89557-0104, USA.
Mol Ther. 2005 Oct;12(4):754-62. doi: 10.1016/j.ymthe.2005.05.011.
The recent observation of vector sequences in the semen of men undergoing clinical gene therapy for hemophilia has highlighted the need to evaluate the risk of inadvertent germ-line transduction in a clinically relevant animal model. In the present study, we used three different approaches to investigate whether the germ line is at risk of inadvertent alteration following in utero retroviral gene transfer in the clinically relevant, random-bred sheep model. First, we conducted breeding studies. All organs from the 10 resultant offspring were devoid of proviral DNA, suggesting that the germ line had not been altered. As a second approach, we performed PCR on gradient-enriched, forensically purified sperm cells from in utero-transduced rams. The purified sperm cells from 6 of 19 of these rams were PCR positive for provirus, providing compelling evidence that the germ line had been transduced. As a third approach, we performed immunohistochemistry on sections of the testis from in utero-transduced sheep. Numerous somatic cells and very low levels of germ cells within the male reproductive tissues were transduced. In conclusion, our analysis on over 3 x 10(9) sperm cells suggests that the direct-injection approach employed in these studies may result in the inadvertent transduction of very low numbers of male germ cells.
最近在接受血友病临床基因治疗的男性精液中观察到载体序列,这突出表明有必要在临床相关的动物模型中评估意外种系转导的风险。在本研究中,我们采用三种不同方法来研究在临床相关的随机繁殖绵羊模型中,子宫内逆转录病毒基因转移后种系是否有意外改变的风险。首先,我们进行了繁殖研究。10只后代的所有器官都没有前病毒DNA,这表明种系未发生改变。作为第二种方法,我们对子宫内转导公羊的梯度富集、法医纯化的精子细胞进行了PCR。这些公羊中有19只,其中6只的纯化精子细胞前病毒PCR呈阳性,这提供了令人信服的证据,证明种系已被转导。作为第三种方法,我们对子宫内转导绵羊的睾丸切片进行了免疫组织化学分析。雄性生殖组织内有许多体细胞和极低水平的生殖细胞被转导。总之,我们对超过3×10⁹个精子细胞的分析表明,这些研究中采用的直接注射方法可能会导致极少量雄性生殖细胞的意外转导。