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作 者:夏书奇 王增松 王翠玲 揭燕 谢飞群 曾振飞 段祥 张宜俊
机构地区:[1]广州市恺泰生物科技有限公司,广州510620
出 处:《实验动物与比较医学》2009年第5期293-297,共5页Laboratory Animal and Comparative Medicine
摘 要:目的研究白细胞介素-12(IL-12)对乙肝病毒表面抗原(HBsAg)疫苗的免疫增强作用。方法选用C57BL/6J小鼠,使用不同剂量的重组鼠白细胞介素-12(rmlL-12)和HBsAg联合给药,检测给药前后血清中IFN-1,的浓度以及给药后小鼠脾脏淋巴细胞对HBsAg刺激的免疫应答能力的变化。结果高剂量HBsAg和高剂量rmIL-12联合两次给药后,血清中IFN-γ浓度明显高于单独给HBsAg组或rmIL-12组(P〈0.05);高剂量联合给药组的小鼠脾脏淋巴细胞经HBsAg体外刺激后诱生IFN-γ的能力明显高于单独给HBsAg组或rmlL-12组(P〈0.05),流式细胞检测分析表明IFN-γ主要来源于CD4^+和CD8^+的T细胞。结论rmlL-12能快速明显地提高C57BL/6J小鼠对HBsAg的特异性免疫应答能力,为IL-12和HBsAg在临床上联合治疗慢性乙肝感染提供了理论依据。Objective To investigate the enhanced immunity of hepatitis B surface antigen (HBsAg) vaccine in response to interleukin-12 (IL-12) stimulation. Method C57BL/6J mice were injected with rmlL-12 plus HBsAg combination, after which the serum IFN-γ level as well as the response of murine spleen lymphocytes to HBsAg was detected. Results Serum IFN-γ level in high dose combination of HBsAg and rmlL-12 group after two injections was significant higher than that in HBsAg or rmlL-12 alone (P〈0.05). The ability of murine spleen lymphocytes producing IFN-γ in response to HBsAg was significantly improved (P〈0.05), and IFN-y mainly originated from CD4^+ & CD8^+ T cells detected by flow cytometric analysis. Conclusion The immunity response of C57BL/6J mice to HBsAg can be rapidly and specifically enhanced by rmlL-12, which may be a reference of IL-12 plus HBsAg clinical application on CHB infection.
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