Yang J S, Kim J J, Hwang D, Choo A Y, Dang K, Maguire H, Kudchodkar S, Ramanathan M P, Weiner D B
Department of Pathology and Laboratory Medicine, University of Pennsylvania, Philadelphia, PA 19104-6100, USA.
J Infect Dis. 2001 Oct 1;184(7):809-16. doi: 10.1086/323395. Epub 2001 Aug 29.
West Nile virus (WNV) is a vectorborne pathogen that induces brain inflammation and death. Recently, confirmed cases of infection and deaths have occurred in the United States Mid-Atlantic region. In this study, a DNA vaccine encoding the WNV capsid protein was constructed, and the in vivo immune responses generated were investigated in DNA vaccine-immunized mice. Antigen-specific humoral and cellular immune responses were observed, including a potent induction of antigen-specific Th1 and cytotoxic T lymphocyte responses. Strong induction of Th1-type immune responses included high levels of antigen-specific elaboration of the Th1-type cytokines interferon-gamma and interleukin-2 and beta-chemokines RANTES (regulated upon activation, normal T cell-expressed and secreted) and macrophage inflammatory protein-1beta. Dramatic infiltration of CD4 and CD8 T cells and macrophages also was observed at the muscle injection site. These results support the potential utility of this method as a tool for developing immunization strategies for WNV and other emerging pathogens.
西尼罗河病毒(WNV)是一种通过媒介传播的病原体,可引发脑部炎症并导致死亡。近期,美国中大西洋地区出现了确诊感染病例和死亡病例。在本研究中,构建了一种编码WNV衣壳蛋白的DNA疫苗,并在经DNA疫苗免疫的小鼠中研究了其产生的体内免疫反应。观察到了抗原特异性体液免疫和细胞免疫反应,包括对抗原特异性Th1和细胞毒性T淋巴细胞反应的有效诱导。Th1型免疫反应的强烈诱导包括高水平的Th1型细胞因子干扰素-γ和白细胞介素-2以及β趋化因子RANTES(活化时调节、正常T细胞表达和分泌)和巨噬细胞炎性蛋白-1β的抗原特异性分泌。在肌肉注射部位还观察到CD4和CD8 T细胞以及巨噬细胞的大量浸润。这些结果支持了该方法作为开发针对WNV和其他新出现病原体的免疫策略工具的潜在效用。