Gao Jimin, Huang Shuqi, Li Ming, Luo Rongcheng, Wang Xiaoning, Takashima Akira
Institute of Molecular Immunology, College of Biotechnology, Southern Medical University, 1838 Guangzhou Dadao Bei, Guangzhou, Guangdong 510515, China.
Vaccine. 2006 Jun 19;24(25):5265-8. doi: 10.1016/j.vaccine.2006.04.031. Epub 2006 May 4.
Through the specific and tight interaction between streptavidin and biotin, a novel platform was developed to allow for rapid (less than 2h), efficient and durable display of streptavidin-tagged bioactive GM-CSF on the surface of biotinylated B16.F10 tumor cells. This technology involved biotinylation of the cell membrane with a biotin derivative and surface modification of the biotinylated cells with the bi-functional fusion protein, streptavidin-tagged GM-CSF. Furthermore, the resultant GM-CSF-modified B16.F10 whole tumor cell vaccine could induce strong and long-lasting systemic protection against the wild-type tumor challenge. Therefore, the platform may represent a fast, efficient and safe approach for the whole tumor cell vaccination.
通过链霉亲和素与生物素之间特异性且紧密的相互作用,开发了一种新型平台,可在生物素化的B16.F10肿瘤细胞表面快速(少于2小时)、高效且持久地展示链霉亲和素标记的生物活性GM-CSF。该技术包括用生物素衍生物对细胞膜进行生物素化,并用双功能融合蛋白(链霉亲和素标记的GM-CSF)对生物素化细胞进行表面修饰。此外,所得的GM-CSF修饰的B16.F10全肿瘤细胞疫苗可诱导针对野生型肿瘤攻击的强大且持久的全身保护作用。因此,该平台可能代表了一种用于全肿瘤细胞疫苗接种的快速、高效且安全的方法。