Induction of immunity by DNA vaccination: application to influenza and tuberculosis.

Behring Institute Mitteilungen Pub Date : 1997-02-01
J B Ulmer, R R Deck, C M DeWitt, J J Donnelly, A Friedman, D L Montgomery, A M Yawman, I M Orme, O Denis, J Content, K Huygen, M A Liu
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Abstract

DNA vaccination is an effective means of inducing both humoral and cell-mediated immunity in animal models of infectious disease. Presented here are data generated in two distinct disease models; one viral (influenza) and one bacterial (tuberculosis). Specifically, plasmid DNA encoding an influenza virus antigen (nucleoprotein; NP) and a Mycobacterium tuberculosis antigen (antigen 85; Ag85) were prepared and tested as DNA vaccines in mice. In both cases, high titer antibody responses and robust cell-mediated immune responses were induced against the respective antigens. With respect to the latter, lymphocyte proliferation, Th1-type cytokine secretion, and cytotoxic T lymphocyte responses were observed upon restimulation with antigen in vitro. Furthermore, protective efficacy in animal challenge models was demonstrated in both systems. The data support the hypothesis that DNA vaccination will prove to be a broadly applicable technique for inducing immunity against various infectious diseases.

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DNA疫苗诱导免疫:在流感和肺结核中的应用。
在传染病动物模型中,DNA疫苗接种是诱导体液免疫和细胞免疫的有效手段。这里展示的是两种不同疾病模型产生的数据;一种是病毒(流感),一种是细菌(肺结核)。具体来说,编码流感病毒抗原的质粒DNA(核蛋白;NP)和结核分枝杆菌抗原(抗原85;Ag85)作为DNA疫苗制备并在小鼠体内进行试验。在这两种情况下,针对各自的抗原诱导高滴度抗体反应和强大的细胞介导免疫反应。后者经抗原体外再刺激后,观察淋巴细胞增殖、th1型细胞因子分泌和细胞毒性T淋巴细胞反应。此外,在动物攻击模型中,两种系统都证明了保护作用。这些数据支持这样的假设,即DNA疫苗接种将被证明是一种广泛适用的技术,可诱导对各种传染病的免疫。
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