Dai Y, Schwarz E M, Gu D, Zhang W W, Sarvetnick N, Verma I M
Molecular Biology and Virology Laboratory, Salk Institute, San Diego, CA 92186-5800.
Proc Natl Acad Sci U S A. 1995 Feb 28;92(5):1401-5. doi: 10.1073/pnas.92.5.1401.
Recombinant adenoviruses containing the canine factor IX (FIX) cDNA were directly introduced in the hind leg muscle of mice. We show that (i) in nude mice, high expression (1-5 micrograms/ml in plasma) of FIX protein can be detected for > 300 days; (ii) in contrast, expression of FIX protein was transient (7-10 days) in normal mice; (iii) CD8+ lymphocytes could be detected within 3 days in the infected muscle tissue; (iv) use of beta 2-microglobulin and immunoglobulin M heavy chain "knockout" mice showed that lack of sustained expression of FIX protein is due to cell-mediated and humoral immune responses; (v) normal mice, once infected with recombinant adenovirus, could not be reinfected efficiently for at least 30 days due to neutralizing viral antibodies; and, finally, (vi) using immunosuppressive drugs, some normal mice can be tolerized to produce and secrete FIX protein for > 5 months. We conclude that currently available adenoviral vectors have serious limitations for use for long-term gene therapy.
含有犬因子IX(FIX)cDNA的重组腺病毒被直接导入小鼠的后腿肌肉。我们发现:(i)在裸鼠中,可检测到FIX蛋白的高表达(血浆中为1 - 5微克/毫升)持续超过300天;(ii)相比之下,FIX蛋白在正常小鼠中的表达是短暂的(7 - 10天);(iii)在感染的肌肉组织中3天内可检测到CD8 +淋巴细胞;(iv)使用β2 -微球蛋白和免疫球蛋白M重链“敲除”小鼠表明,FIX蛋白缺乏持续表达是由于细胞介导和体液免疫反应;(v)正常小鼠一旦感染重组腺病毒,由于中和病毒抗体,至少30天内不能有效再次感染;最后,(vi)使用免疫抑制药物,一些正常小鼠可以被耐受以产生和分泌FIX蛋白超过5个月。我们得出结论,目前可用的腺病毒载体在长期基因治疗中的应用存在严重局限性。