Wood M J, Charlton H M, Wood K J, Kajiwara K, Byrnes A P
Dept of Human Anatomy, Oxford University, UK.
Trends Neurosci. 1996 Nov;19(11):497-501. doi: 10.1016/S0166-2236(96)10060-6.
Non-replicating adenovirus vectors are being developed as vehicles for gene transfer into cells of the nervous system. An important requirement for successful gene transfer is the absence of deleterious cytotoxic or inflammatory side effects of the delivery system. Despite offering relatively stable reporter gene expression, currently available adenovirus vectors also elicit immune responses in the brain, both at the site of vector delivery and at synaptically linked distant sites. However, although an anti-viral T-lymphocyte response eliminates the vector and damages local tissue in many peripheral organs, the immune response to adenovirus in the brain is less effective and enables the vector to persist. Nevertheless, in this persistent state the adenovirus vector remains a potential target for a destructive immune response that can also cause local demyelination. The development of strategies to minimize this damaging immune response, through either vector modification or immunomodulation, will be crucial for the future success of genetic therapies in the brain.
非复制型腺病毒载体正被开发用作将基因导入神经系统细胞的载体。成功进行基因转移的一个重要要求是递送系统不存在有害的细胞毒性或炎症副作用。尽管目前可用的腺病毒载体能提供相对稳定的报告基因表达,但它们在脑内的载体递送部位以及突触连接的远处部位都会引发免疫反应。然而,虽然抗病毒T淋巴细胞反应会清除载体并损害许多外周器官的局部组织,但脑内对腺病毒的免疫反应效果较差,使得载体能够持续存在。尽管如此,在这种持续状态下,腺病毒载体仍然是可能引发破坏性免疫反应的潜在靶点,这种反应也可能导致局部脱髓鞘。通过载体修饰或免疫调节来制定策略以尽量减少这种破坏性免疫反应,对于未来脑内基因治疗的成功至关重要。