Translational Research Laboratory, Institut Català d'Oncologia-IDIBELL, L'Hospitalet de Llobregat, Barcelona, Spain.
Adv Cancer Res. 2012;115:93-114. doi: 10.1016/B978-0-12-398342-8.00004-5.
During the last decade adenovirus has lost its appeal in gene therapy due to a high immunogenicity that leads to a transient gene expression. However, adenovirus has gained attention as replication-competent vector to treat cancer. Designed for virotherapy, adenovirus has been successfully modified to replicate selectively in tumor cells. After the initial clinical trials with tumor-selective adenoviruses, it has become clear that further improvements on tumor targeting, intratumoral dissemination, and modulation of antiviral and antitumor immune responses are needed to effectively treat cancer. The non-viral delivery of infectious DNA encoding an oncolytic adenovirus armed with extracellular matrix-degrading genes and with genes that regulate the immune system to favor antitumor instead of antiviral immunity are key in the design oncolytic adenovirus.
在过去的十年中,腺病毒由于其高度的免疫原性导致短暂的基因表达,因此在基因治疗中的应用受到了影响。然而,腺病毒作为一种复制型载体,在治疗癌症方面引起了人们的关注。为了进行病毒治疗,腺病毒已经被成功地改造成能够在肿瘤细胞中选择性复制。在进行了具有肿瘤选择性的腺病毒的初步临床试验后,人们清楚地认识到,需要进一步提高肿瘤靶向性、肿瘤内扩散能力以及调节抗病毒和抗肿瘤免疫反应,才能有效地治疗癌症。非病毒传递携带细胞外基质降解基因和调节免疫系统的抗肿瘤免疫而不是抗病毒免疫的溶瘤腺病毒的传染性 DNA,是设计溶瘤腺病毒的关键。