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Vaxfectin增强了约氏疟原虫环子孢子DNA疫苗的免疫原性和保护效力。

Vaxfectin enhances immunogenicity and protective efficacy of P. yoelii circumsporozoite DNA vaccines.

作者信息

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

机构信息

Malaria Program, Naval Medical Research Center, 503 Robert Grant Avenue, Silver Spring, MD 20910-7500, USA.

出版信息

Vaccine. 2006 Mar 10;24(11):1921-7. doi: 10.1016/j.vaccine.2005.10.041. Epub 2005 Nov 2.

Abstract

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.

摘要

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。

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