Department of Hematology, Hemostaseology, Oncology and Stem Cell Transplantation, Hannover Medical School, Hannover, Germany.
Expert Rev Vaccines. 2010 Mar;9(3):309-21. doi: 10.1586/erv.10.9.
Lentiviruses are retroviruses that are able to transduce both dividing and nondividing cells. Dendritic cells are key players in the innate and adaptive immune responses, and are natural targets for lentiviruses. Lentiviral vectors (LVs) have recently reached the clinical gene therapy arena, prompting their use as clinical vaccines. In recent years, LVs have emerged as a robust and practical experimental platform for gene delivery and rational genetic reprogramming of dendritic cells. Here, we present the status quo of the LV system for protective or therapeutic vaccine development. This vector system has been extensively evaluated for ex vivo and in vivo (immuno)gene delivery. Improvements of the LV design in order to further grant a higher biosafety profile for vaccine development are presented.
慢病毒是能够转导分裂和非分裂细胞的逆转录病毒。树突状细胞是先天和适应性免疫反应的关键参与者,也是慢病毒的天然靶标。慢病毒载体 (LV) 最近进入了临床基因治疗领域,促使它们被用作临床疫苗。近年来,LV 已成为基因传递和树突状细胞合理遗传重编程的强大而实用的实验平台。在这里,我们介绍了用于保护性或治疗性疫苗开发的 LV 系统的现状。该载体系统已广泛用于体外和体内 (免疫)基因传递的评估。为了进一步提高疫苗开发的生物安全性,提出了对 LV 设计的改进。