Batra Lalit, Verma Shailendra K, Nagar Durgesh P, Saxena Nandita, Pathak Prachi, Pant Satish C, Tuteja Urmil
Microbiology Division, Defence Research & Development Establishment, Gwalior, India.
Pharmacology and Toxicology Division, Defence Research & Development Establishment, Gwalior, India.
PLoS Negl Trop Dis. 2014 Dec 4;8(12):e3322. doi: 10.1371/journal.pntd.0003322. eCollection 2014 Dec.
No ideal vaccine exists to control plague, a deadly dangerous disease caused by Yersinia pestis. In this context, we cloned, expressed and purified recombinant F1, LcrV antigens of Y. pestis and heat shock protein70 (HSP70) domain II of M. tuberculosis in E. coli. To evaluate the protective potential of each purified protein alone or in combination, Balb/C mice were immunized. Humoral and cell mediated immune responses were evaluated. Immunized animals were challenged with 100 LD50 of Y. pestis via intra-peritoneal route. Vaccine candidates i.e., F1 and LcrV generated highly significant titres of anti-F1 and anti-LcrV IgG antibodies. A significant difference was noticed in the expression level of IL-2, IFN-γ and TNF-α in splenocytes of immunized animals. Significantly increased percentages of CD4+ and CD8+ T cells producing IFN-γ in spleen of vaccinated animals were observed in comparison to control group by flow cytometric analysis. We investigated whether the F1, LcrV and HSP70(II) antigens alone or in combination can effectively protect immunized animals from any histopathological changes. Signs of histopathological lesions noticed in lung, liver, kidney and spleen of immunized animals on 3rd day post challenge whereas no lesions in animals that survived to day 20 post-infection were observed. Immunohistochemistry showed bacteria in lung, liver, spleen and kidney on 3rd day post-infection whereas no bacteria was observed on day 20 post-infection in surviving animals in LcrV, LcrV+HSP70(II), F1+LcrV, and F1+LcrV+HSP70(II) vaccinated groups. A significant difference was observed in the expression of IL-2, IFN-γ, TNF-α, and CD4+/CD8+ T cells secreting IFN-γ in the F1+LcrV+HSP70(II) vaccinated group in comparison to the F1+LcrV vaccinated group. Three combinations that included LcrV+HSP70(II), F1+LcrV or F1+LcrV+HSP70(II) provided 100% protection, whereas LcrV alone provided only 75% protection. These findings suggest that HSP70(II) of M. tuberculosis can be a potent immunomodulator for F1 and LcrV containing vaccine candidates against plague.
目前尚无理想的疫苗可用于控制鼠疫,这是一种由鼠疫耶尔森菌引起的致命危险疾病。在此背景下,我们在大肠杆菌中克隆、表达并纯化了鼠疫耶尔森菌的重组F1、LcrV抗原以及结核分枝杆菌的热休克蛋白70(HSP70)结构域II。为了评估每种纯化蛋白单独或联合使用时的保护潜力,对Balb/C小鼠进行了免疫接种。评估了体液免疫和细胞介导的免疫反应。通过腹腔途径用100个半数致死剂量(LD50)的鼠疫耶尔森菌对免疫动物进行攻击。候选疫苗F1和LcrV产生了高滴度的抗F1和抗LcrV IgG抗体。在免疫动物的脾细胞中,白细胞介素-2(IL-2)、干扰素-γ(IFN-γ)和肿瘤坏死因子-α(TNF-α)的表达水平存在显著差异。通过流式细胞术分析发现,与对照组相比,接种疫苗动物脾脏中产生IFN-γ的CD4+和CD8+ T细胞百分比显著增加。我们研究了F1、LcrV和HSP70(II)抗原单独或联合使用是否能有效保护免疫动物免受任何组织病理学变化的影响。在攻击后第3天,在免疫动物的肺、肝、肾和脾脏中发现了组织病理学损伤的迹象,而在感染后存活至第20天的动物中未观察到损伤。免疫组织化学显示,在感染后第3天,肺、肝、脾和肾中有细菌,而在LcrV、LcrV + HSP70(II)、F1 + LcrV和F1 + LcrV + HSP70(II)接种组中,存活动物在感染后第20天未观察到细菌。与F1 + LcrV接种组相比,F1 + LcrV + HSP70(II)接种组中IL-2、IFN-γ、TNF-α以及分泌IFN-γ的CD4+/CD8+ T细胞的表达存在显著差异。包括LcrV + HSP70(II)、F1 + LcrV或F1 + LcrV + HSP70(II)的三种组合提供了100%的保护,而单独的LcrV仅提供75%的保护。这些发现表明,结核分枝杆菌的HSP70(II)对于含F1和LcrV的鼠疫候选疫苗可能是一种有效的免疫调节剂。