Yu Da-Hai, Hu Xi-Dan, Cai Hong
The National Laboratory of Protein Engineering and Plant Genetic Engineering, Peking University, Beijing, China.
DNA Cell Biol. 2007 Jun;26(6):435-43. doi: 10.1089/dna.2006.0552.
We constructed a combined DNA vaccine comprising genes encoding the antigens BCSP31, superoxide dismutase (SOD), and L7/L12 and evaluated its immunogenicity and protective efficacy. Immunization of mice with the combined DNA vaccine offered high protection against Brucella abortus (B. abortus) infection. The vaccine induced a vigorous specific immunoglobulin G (IgG) response, with higher IgG2a than IgG1 titers. Cytokine profiling performed at the same time showed a biased Th1-type immune response with significantly increased interferon-gamma and tumor necrosis factor-alpha stimulation. CD8(+), but not CD4(+), T cells accumulated at significantly higher levels after administration of the vaccine. Granzyme B-producing CD8(+) T cells were significantly higher in number in samples prepared from combined DNA-vaccinated mice compared with S19-vaccinated mice, demonstrating that the cytotoxicity lysis pathway is involved in the response to Brucella infection. The success of our combined DNA vaccine in a mouse model suggests its potential efficacy against brucellosis infection in large animals.
我们构建了一种包含编码抗原BCSP31、超氧化物歧化酶(SOD)和L7/L12基因的联合DNA疫苗,并评估了其免疫原性和保护效力。用联合DNA疫苗免疫小鼠可提供对流产布鲁氏菌(B. abortus)感染的高度保护。该疫苗诱导了强烈的特异性免疫球蛋白G(IgG)反应,IgG2a滴度高于IgG1。同时进行的细胞因子分析显示偏向Th1型免疫反应,干扰素-γ和肿瘤坏死因子-α刺激显著增加。接种疫苗后,CD8(+) T细胞而非CD4(+) T细胞的积累水平显著更高。与接种S19疫苗的小鼠相比,联合DNA疫苗接种小鼠制备的样本中产生颗粒酶B的CD8(+) T细胞数量显著更多,表明细胞毒性裂解途径参与了对布鲁氏菌感染的反应。我们的联合DNA疫苗在小鼠模型中的成功表明其对大型动物布鲁氏菌病感染具有潜在效力。