Jimenez Gretchen S, Planchon Rodrick, Wei Qun, Rusalov Denis, Geall Andrew, Enas Joel, Lalor Peggy, Leamy Vicky, Vahle Ruth, Luke Catherine J, Rolland Alain, Kaslow David C, Smith Larry R
Vical Incorporated, San Diego, California 92121, USA.
Hum Vaccin. 2007 Sep-Oct;3(5):157-64. doi: 10.4161/hv.3.5.4175. Epub 2007 Mar 20.
Next generation influenza vaccines containing conserved antigens may enhance immunity against seasonal or pandemic influenza virus strains. Using a plasmid DNA (pDNA)-based vaccine approach, we systematically tested combinations of NP, M1, and M2 antigens derived from consensus sequences for protection against lethal influenza challenge and compared formulations for adjuvanting low pDNA vaccine doses. The highest level of protection at the lowest pDNA doses was provided by Vaxfectin-formulated NP + M2. Vaxfectin adjuvanticity was confirmed with a low dose of HA pDNA. These promising proof-of-concept data support the clinical development of Vaxfectin-formulated pDNA encoding NP + M2 consensus proteins.
含有保守抗原的下一代流感疫苗可能会增强针对季节性或大流行性流感病毒株的免疫力。我们采用基于质粒DNA(pDNA)的疫苗方法,系统地测试了源自共有序列的NP、M1和M2抗原组合对致死性流感攻击的保护作用,并比较了用于佐剂低剂量pDNA疫苗的配方。Vaxfectin配方的NP + M2在最低pDNA剂量下提供了最高水平的保护。低剂量HA pDNA证实了Vaxfectin的佐剂活性。这些有前景的概念验证数据支持Vaxfectin配方的编码NP + M2共有蛋白的pDNA的临床开发。