恶性疟原虫海南FCC1/HN株CSP抗CSP抗原基因在Hela细胞中表达产物的免疫应答研究
Immune responses to the expressed products of the CSP antigen gene of Plasmodium falciparum southern China isolate FCC1/HN in Hela cell
摘要目的本课题利用含人类巨细胞病毒(CMV)的高效启动子和增强子的pcDNA3质粒作为载体,在人宫颈癌细胞(Hela)中高效表达恶性疟原虫环子孢子蛋白(CSP),观察其表达产物诱导BALB/c小鼠的免疫应答水平。方法从我国恶性疟原虫海南FCC1/HN株基因组中特异扩增CSP基因;将其定向克隆到真核表达质粒pcDNA3的CMV启动子下游,构建重组质粒pcDNA3-PfCSP,并导入Hela细胞;分离和纯化表达蛋白,并将其免疫接种BALB/c小鼠;通过ELISA、Dot-ELISA、Western blot分析、T淋巴细胞增殖试验、自然杀伤(NK)细胞活性检测、T淋巴细胞亚群测定,观察其诱导BALB/c小鼠产生体液免疫和细胞免疫的应答水平。结果免疫后的小鼠产生高效价的特异性抗体反应,ELISA检测抗体滴度达1∶6400;Western blot结果在38.3?kDa相应位置处出现较清晰的显色条带。小鼠脾淋巴细胞转化试验结果显示,且表达蛋白抗原刺激免疫鼠和正常鼠测得OD值分别为0.34±0.04和0.12±0.03,两者之间差异显著(P<0.01)。用MTT比色分析法检测小鼠NK细胞活性,免疫鼠NK细胞活性明显高于正常鼠(P<0.05)。用间接免疫荧光法测定免疫鼠淋巴细胞亚群,结果表明其CD4+、CD8+T细胞数与正常鼠相比,均明显增多,经t检验差异显著(P<0.05)。结论恶性疟原虫FCC1/NH株CSP基因表达产物能特异性刺激BALB/c小鼠产生较强的体液免疫和细胞免疫反应,并有提高小鼠NK细胞活性的作用,增强其抗感染的免疫应答能力。
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abstractsObjective To construct a eukaryotic expression system with pcDNA3-PfCSP/Hela for the Circumsporozoite protein (CSP) gene of Plasmodium falciparum (P. falciparum), to observe the immune responses in BALB/c mice induced by the expressed proteins. Methods The recombinant plasmid pcDNA3-PfCSP was transformed into the Hela cell line. The expressed protein was isolated and analyzed by using SDS-PAGE and used for immunization of BALB/c mice by subcutaneous, intravenous, and intraperitoneal adminstration. Enzyme-linked immunosorbent assay(ELISA), Dot-ELISA, Western blot, T lymphocyte proliferation test, natural killer cell(NKC) activity assay, and CD4+ and CD8+ T cell detection were used for observation of humoral and cellular immune responses. Results Immune sera strongly reacted with the expressed protein, antibody titer was up to 1∶6400 as detected by ELISA. Western blot analysis revealed a specific band at 38.3?Kda. When the spleen cells of normal and immunized BALB/c mice were specifically stimulated with expressed protein, the optical densities were 0.12±0.03 and 0.34±0.04, respectively. The latter were significantly higher than the former (P<0.01). We used the MTT colorimetric assay to measure NKC activity of mice spleen. The results showed that the NKC activity of immunized BALB/c mice was remarkably higher than that of the controls (P<0.05). CD4+ and CD8+ T cells were detected by using monoclonal antibody immunofluorescence methods. The results showed that the percentage of CD4+ and CD8+ T cells of immunized group were significantly higher than that of control group (P<0.05).Conclusions The humoral and cell-mediated immune responses and elevated NKC activity to products made with a eukaryotic expression system could be specifically detected in BALB/c mice. These findings indicate that the expressed protein could enhance the immune function in mice.
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