Sedegah Martha, Rogers William O, Belmonte Arnel, Belmonte Maria, Banania Glenna, Patterson Noelle, Ferrari Marilyn, Kaslow David C, Carucci Daniel J, Richie Thomas L, Doolan Denise L
Malaria Program, Naval Medical Research Center, 503 Robert Grant Avenue, Silver Spring, MD 20910-7500, USA.
Vaccine. 2006 Mar 10;24(11):1921-7. doi: 10.1016/j.vaccine.2005.10.041. Epub 2005 Nov 2.
We evaluated the capacity of the cationic lipid based formulation, Vaxfectin, to enhance the immunogenicity and protective efficacy of DNA-based vaccine regimens in the Plasmodium yoelii murine malaria model. We immunized Balb/c mice with varying doses (0.4-50 microg) of plasmid DNA (pDNA) encoding the P. yoelii circumsporozoite protein (PyCSP), either in a homologous DNA/DNA regimen (D-D) or a heterologous prime-boost DNA-poxvirus regimen (D-V). At the lowest pDNA doses, Vaxfectin substantially enhanced IFA titers, ELISPOT frequencies, and protective efficacy. Clinical trials of pDNA vaccines have often used low pDNA doses based on a per kilogram weight basis. Formulation of pDNA vaccines in Vaxfectin may improve their potency in human clinical trials.
我们评估了基于阳离子脂质的制剂Vaxfectin在约氏疟原虫小鼠疟疾模型中增强基于DNA的疫苗方案的免疫原性和保护效力的能力。我们用不同剂量(0.4 - 50微克)编码约氏疟原虫环子孢子蛋白(PyCSP)的质粒DNA(pDNA)免疫Balb/c小鼠,采用同源DNA/DNA方案(D-D)或异源初免-加强DNA-痘病毒方案(D-V)。在最低的pDNA剂量下,Vaxfectin显著提高了免疫荧光分析(IFA)滴度、酶联免疫斑点(ELISPOT)频率和保护效力。pDNA疫苗的临床试验通常基于每千克体重使用低pDNA剂量。用Vaxfectin配制pDNA疫苗可能会提高其在人体临床试验中的效力。