Tite J P, Gao X M, Hughes-Jenkins C M, Lipscombe M, O'Callaghan D, Dougan G, Liew F Y
Department of Experimental Immunobiology, Wellcome Biotech, Beckenham, Kent, U.K.
Immunology. 1990 Aug;70(4):540-6.
A plasmid encoding the influenza nucleoprotein gene from A/NT/60/68 virus was transduced into the attenuated Salmonella typhimurium aroA- strain SL3261. The bacterial vector expressing the viral gene product was able to induce both humoral and cell-mediated immune responses to the nucleoprotein antigen. CD4+ virus-specific T cells capable of proliferation were readily induced and, in some circumstances, class II major histocompatibility complex (MHC)-restricted cytotoxicity was detected. However, virus-specific class I MHC-restricted cytotoxic T lymphocytes (CTL) were not detected after such immunization. Mice immunized orally with the nucleoprotein-expressing bacteria mounted a strong anti-viral antibody response and spleen cells from such mice proliferated specifically to virus challenge in vitro, producing interferon-gamma (IFN-gamma) and interleukin-2 (IL-2). Orally immunized mice showed significant protection from challenge infection with influenza virus if the mice were also boosted intranasally before infection.
将编码A/NT/60/68病毒流感核蛋白基因的质粒转导至减毒鼠伤寒沙门氏菌aroA-菌株SL3261中。表达病毒基因产物的细菌载体能够诱导针对核蛋白抗原的体液免疫和细胞介导的免疫反应。能够增殖的CD4+病毒特异性T细胞很容易被诱导产生,并且在某些情况下,还检测到了II类主要组织相容性复合体(MHC)限制的细胞毒性。然而,这种免疫后未检测到病毒特异性I类MHC限制的细胞毒性T淋巴细胞(CTL)。用表达核蛋白的细菌经口免疫的小鼠产生了强烈的抗病毒抗体反应,并且来自此类小鼠的脾细胞在体外受到病毒攻击时会特异性增殖,产生γ干扰素(IFN-γ)和白细胞介素-2(IL-2)。如果在感染前还对经口免疫的小鼠进行鼻内加强免疫,则这些小鼠对流感病毒攻击表现出显著的保护作用。