Hsp70 DNA 疫苗与 Hsp65 DNA 疫苗对人类结核分枝杆菌免疫原性的比较研究。

W Dai, H Huang, Y Yuan, J Hu, Y Huangfu
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引用次数: 0

摘要

用人型结核分枝杆菌中的 Hsp70 DNA 和 Hsp65 DNA 疫苗对 BALB/c 小鼠进行免疫。免疫八周后,摘除眼球,取血和脾脏,收获腹腔巨噬细胞。淋巴细胞刺激指数(SI)用于测量细胞增殖能力,NO 释放量用于测量巨噬细胞的吞噬活性。用 ELISA 试剂盒检测血清和脾脏淋巴细胞培养上清中的白细胞介素-2(IL-2)和干扰素-γ(IFN-γ)水平。结果表明,小鼠肌肉注射100微克/小鼠的Hsp70 DNA疫苗后,脾脏淋巴细胞增殖能力明显高于对照组、载体组和Hsp65 DNA疫苗组(P < 0.01);小鼠腹腔巨噬细胞中NO的含量明显低于对照组和Hsp65 DNA疫苗组(P < 0.01);小鼠血清IL-2含量明显高于对照组,但Hsp65 DNA组与载体组无统计学差异(P > 0.05);小鼠血清IFN-γ含量明显高于对照组,但明显低于Hsp65 DNA疫苗组(P < 0.05)。结果表明,Hsp70 DNA疫苗免疫可明显增强小鼠的免疫应答,但其免疫强度似乎不如Hsp65 DNA疫苗。Hsp70 DNA疫苗和Hsp65 DNA疫苗的抗感染机制和未来的临床应用值得进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Comparative study on the immunogenicity between Hsp70 DNA vaccine and Hsp65 DNA vaccine in human Mycobacterium tuberculosis.

The BALB/c mice were immunized with Hsp70 DNA and Hsp65 DNA vaccines in human Mycobacterium tuberculosis. Eight weeks after immunization, the eyeballs were removed, blood and spleen taken, and intraperitoneal macrophages were harvested. The lymphocytic stimulating index (SI) was used to measure the cellular proliferating ability and NO release to measure the phagocytic activity of the macrophages. With ELISA kit, the levels of interleukin-2 (IL-2) and interferon-gamma (IFN-gamma) in serum and the splenic lymphocytic cultured supernatant were detected. The results showed that after the mice were immunized with 100 micrograms/mouse of Hsp70 DNA vaccine intramuscularly, the splenic lymphocytic proliferating ability in the mice was significantly increased as compared with that in the control group, vector group and Hsp65 DNA vaccine group (P < 0.01); The contents of NO in the intraperitoneal macrophages of the mice were significantly lower than in the control group and Hsp65 DNA vaccine group (P < 0.01); The levels of serum IL-2 in the mice were significantly higher than in the control group, but there was no statistical difference between Hsp65 DNA group and vector group (P > 0.05); The contents of serum IFN-gamma in the mice were significantly higher than in the control group, but significantly lower than in the Hsp65 DNA vaccine group (P < 0.05). It was indicated that immunization with Hsp70 DNA vaccine could obviously enhance the immune response, but its intensity seemed inferior to Hsp65 DNA vaccine. The anti-infection mechanisms and clinical use in the future of the vaccines of Hsp70 DNA and Hsp65 DNA are worth further studying.

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