Lasaro Marcio O, Diniz Mariana O, Reyes-Sandoval Arturo, Ertl Hildegund C, Ferreira Luis C S
Department of Microbiology, Institute of Biomedical Sciences, University of São Paulo, SP, 05508-900, Brazil.
Microbes Infect. 2005 Dec;7(15):1541-50. doi: 10.1016/j.micinf.2005.05.024. Epub 2005 Sep 9.
DNA vaccines encoding the human papillomavirus type-16 (HPV-16) E6 and E7 oncoproteins genetically fused to the human herpes simplex virus type 1 (HSV-1) gD protein were tested in mice for induction of T cell-mediated immunity and protection against tumor cell challenge. Hybrid genes, generated after insertion of E6 or E7-encoding sequences into internal sites of the gD-encoding gene, were transcribed in vitro and the chimeric proteins were expressed at the surface of in vitro-transfected mammalian cells. Female C57BL/6 mice immunized with 4 intramuscular doses (100 microg of DNA/dose) of the DNA vaccines encoding E7 efficiently generated E7-specific CD8(+) T cells. Vaccination of mice with the DNA vaccines encoding the E7, or both E6 and E7, conferred complete protection to challenges from TC-1 tumor cells and partial therapeutic effect (40%) in mice inoculated with TC-1 cells on the same day or 5 days prior to the first vaccine dose.
将编码人乳头瘤病毒16型(HPV-16)E6和E7癌蛋白并与人单纯疱疹病毒1型(HSV-1)gD蛋白基因融合的DNA疫苗在小鼠中进行测试,以诱导T细胞介导的免疫反应并抵御肿瘤细胞攻击。将编码E6或E7的序列插入编码gD的基因内部位点后产生的杂交基因在体外转录,嵌合蛋白在体外转染的哺乳动物细胞表面表达。用4剂肌肉注射(每剂100微克DNA)编码E7的DNA疫苗免疫的雌性C57BL/6小鼠有效地产生了E7特异性CD8(+) T细胞。用编码E7或同时编码E6和E7的DNA疫苗对小鼠进行接种,可为其抵御TC-1肿瘤细胞的攻击提供完全保护,并对在首次疫苗接种当天或前5天接种TC-1细胞的小鼠产生部分治疗效果(40%)。