新疆出血热病毒Gc抗原片段的抗原性和免疫原性分析

Jìngyuàn Zhāng, Meifang Wang, Chaofan Guo, Huabing Zhu, Yijie Li, Yujiang Zhang, Sùróng Sūn
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The mice were randomly divided into 5 groups, including pVAX1-GcⅠ+rGcⅠ group, pVAX1-GcⅡ+rGcⅡ group, rGcⅠ group, rGcⅡ group and saline group (control group) with 7 mice in each group. The serum antibody titer of mice was detected by indirect ELISA, and the immune effect was evaluated by spleen T lymphocyte proliferation assay and cytokine content determination. \n \n \nResults \nThe fusion proteins rGcⅠ and rGcⅡ were purified and obtained, which could react with positive serum of sheep and had good antigenicity. After three immunizations, the IgG levels in the serum of each experimental group were significantly higher than those in the control group (all P<0.001). The serum antibody titers of the experimental groups were reached above 1∶12 800. 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引用次数: 0

摘要

目的表达和纯化新疆出血热病毒(XHFV)糖蛋白GcⅠ和GcⅡ两个结构域,并研究其免疫原性和对小鼠免疫应答的影响。方法构建pET28a-GcⅠ和pET32a-GcⅡ原核表达质粒,分别转化大肠杆菌BL21。优化了rGcⅠ和rGcⅡ蛋白的表达和纯化条件。采用Western Blot和酶联免疫吸附试验(ELISA)检测融合蛋白的抗原性。采用蛋白免疫和DNA引物-蛋白增强两种方法对BALB/c小鼠进行免疫。将小鼠随机分为pVAX1-GcⅠ+rGcⅠ组、pVAX1-GcⅡ+rGcⅡ组、rGcⅠ组、rGcⅡ组和生理盐水组(对照组)5组,每组7只。间接ELISA法检测小鼠血清抗体滴度,脾T淋巴细胞增殖试验和细胞因子含量测定评价免疫效果。结果纯化得到的融合蛋白rGcⅠ和rGcⅡ能与羊阳性血清反应,具有良好的抗原性。三次免疫后,各试验组血清IgG水平均显著高于对照组(P<0.001)。试验组血清抗体滴度均在1∶12 800以上。其中,rGcⅡ和pVAX1-GcⅡ+rGcⅡ组脾细胞培养上清中Th2型细胞因子白细胞介素-4 (IL-4)浓度[(79.97±7.47)ng/L]和pVAX1-GcⅡ+rGcⅡ组[(61.43±9.27)ng/L]均显著高于对照组(24.29±3.81)ng/L(均P<0.01)。pVAX1-GcⅡ+rGcⅡ组Th1型细胞因子干扰素-γ (IFN-γ)质量浓度最高[(42.46±2.60)ng/L],显著高于对照组(20.33±1.67)ng/L,差异有统计学意义(P<0.001)。抗原特异性脾T淋巴细胞增殖显著(P<0.001)。结论纯化的重组蛋白rGcⅠ和rGcⅡ具有良好的免疫原性,可使免疫系统T淋巴细胞倾向于Th2应答,pVAX1-GcⅡ与重组蛋白GcⅡ联合可诱导较好的抗原特异性免疫效果。pVAX1-GcⅡ联合重组蛋白GcⅡ有望作为XHFV防控候选疫苗。关键词:新疆出血热病毒;糖蛋白;原核表达;净化;免疫原性
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Antigenicity and immunogenicity analysis of Xinjiang hemorrhagic fever virus Gc antigen fragment
Objective To express and purify two domains GcⅠ and GcⅡ of Xinjiang hemorrhagic fever virus (XHFV) glycoprotein, and to study its immunogenicity and the effects on immune response in mice. Methods The prokaryotic expression plasmids of pET28a-GcⅠ and pET32a-GcⅡ were constructed and transformed into E. coli BL21, respectively. The expression and purification conditions of rGcⅠ and rGcⅡ proteins were optimized. The antigenicity of the fusion protein was detected by Western Blot and enzyme-linked immunosorbent assay (ELISA). BALB/c mice were immunized by protein immunization and DNA priming-protein boosting. The mice were randomly divided into 5 groups, including pVAX1-GcⅠ+rGcⅠ group, pVAX1-GcⅡ+rGcⅡ group, rGcⅠ group, rGcⅡ group and saline group (control group) with 7 mice in each group. The serum antibody titer of mice was detected by indirect ELISA, and the immune effect was evaluated by spleen T lymphocyte proliferation assay and cytokine content determination. Results The fusion proteins rGcⅠ and rGcⅡ were purified and obtained, which could react with positive serum of sheep and had good antigenicity. After three immunizations, the IgG levels in the serum of each experimental group were significantly higher than those in the control group (all P<0.001). The serum antibody titers of the experimental groups were reached above 1∶12 800. Among them, the concentration of Th2 type cytokine interleukin-4 (IL-4) in the spleen cell culture supernatant of rGcⅡ [(79.97±7.47) ng/L] and pVAX1-GcⅡ+rGcⅡ group [(61.43±9.27) ng/L] was significantly higher than (24.29±3.81) ng/L of the control group, respectively (all P<0.01). The highest mass concentration [(42.46±2.60) ng/L] of Th1 type cytokine interferon-γ (IFN-γ) was observed in the pVAX1-GcⅡ+rGcⅡ group, which was significantly higher than (20.33±1.67) ng/L of the control group, and the difference was statistically significant (P<0.001). That showed a significant antigen-specific splenic T lymphocyte proliferation (P<0.001). Conclusions The purified recombinant proteins rGcⅠand rGcⅡhave good immunogenicity, which can make the immune system T lymphocytes tend to Th2 response, and pVAX1-GcⅡ combined with recombinant protein GcⅡ can induce better antigen-specific immune effect. And pVAX1-GcⅡ combined with recombinant protein GcⅡ is expected to be used as vaccine candidates for the prevention and control of XHFV. Key words: Xinjiang hemorrhagic fever virus; Glycoprotein; Prokaryotic expression; Purification; Immunogenicity
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