Mork Family Department of Chemical Engineering and Materials Science, University of Southern California, Los Angeles, California, United States of America.
PLoS One. 2011;6(6):e21491. doi: 10.1371/journal.pone.0021491. Epub 2011 Jun 27.
Lentiviruses have recently attracted considerable interest for their potential as a genetic modification tool for dendritic cells (DCs). In this study, we explore the ability of lentiviruses enveloped with alphaviral envelope glycoproteins derived from Semliki Forest virus (SFV) to mediate transduction of DCs. We found that SFV glycoprotein (SFV-G)-pseudotyped lentiviruses use C-type lectins (DC-SIGN and L-SIGN) as attachment factors for transduction of DCs. Importantly, SFV-G pseudotypes appear to have enhanced transduction towards C-type lectin-expressing cells when produced under conditions limiting glycosylation to simple high-mannose, N-linked glycans. These results, in addition to the natural DC tropism of SFV-G, offer evidence to support the use of SFV-G-bearing lentiviruses to genetically modify DCs for the study of DC biology and DC-based immunotherapy.
慢病毒最近因其作为树突状细胞 (DC) 的基因修饰工具的潜力而引起了相当大的关注。在这项研究中,我们探讨了源自 Semliki Forest 病毒 (SFV) 的包膜糖蛋白包裹的慢病毒转导 DC 的能力。我们发现 SFV 糖蛋白 (SFV-G) 假型慢病毒使用 C 型凝集素 (DC-SIGN 和 L-SIGN) 作为转导 DC 的附着因子。重要的是,在限制糖基化为简单高甘露糖、N 连接聚糖的条件下产生时,SFV-G 假型似乎增强了对 C 型凝集素表达细胞的转导。除了 SFV-G 对 DC 的天然趋向性之外,这些结果为使用携带 SFV-G 的慢病毒来修饰 DC 以用于研究 DC 生物学和基于 DC 的免疫疗法提供了证据支持。