Lundstrom Kenneth
Regulon Inc./BioXtal, Chemin des Croisettes 22, CH-1066 Epalinges, Switzerland.
Expert Opin Biol Ther. 2003 Aug;3(5):771-7. doi: 10.1517/14712598.3.5.771.
Semliki Forest virus (SFV) vectors transduce a broad range of mammalian and non-mammalian cells, generating high levels of transient expression of heterologous proteins. Generally, they induce apoptosis in mammalian host cells, leading to rapid cell death. These features have made SFV attractive for various gene therapy applications. Recombinant particles, naked RNA and plasmid DNA containing SFV replicons, demonstrate a strong immune response against recombinantly expressed proteins, which has shown protection against tumour challenges. Intratumoural injection of SFV particles has resulted in tumour regression. SFV vectors have been used for production of retrovirus-like particles. Recently, encapsulation of SFV particles into liposomes has generated highly efficient targeting to tumours. Novel SFV vectors based on point mutations in the non-structural genes, and avirulent SFV strains, have further widened the application range.
塞姆利基森林病毒(SFV)载体可转导多种哺乳动物和非哺乳动物细胞,使异源蛋白产生高水平的瞬时表达。一般来说,它们会诱导哺乳动物宿主细胞凋亡,导致细胞迅速死亡。这些特性使SFV在各种基因治疗应用中具有吸引力。重组颗粒、含有SFV复制子的裸RNA和质粒DNA,对重组表达的蛋白表现出强烈的免疫反应,已显示出对肿瘤攻击的保护作用。瘤内注射SFV颗粒已导致肿瘤消退。SFV载体已用于生产逆转录病毒样颗粒。最近,将SFV颗粒封装到脂质体中已实现对肿瘤的高效靶向。基于非结构基因点突变的新型SFV载体和无毒SFV毒株,进一步拓宽了应用范围。