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中国防痨杂志 ›› 2008, Vol. 30 ›› Issue (6): 510-514.

• 论著 • 上一篇    下一篇

γ-干扰素联合微卡免疫治疗结核病小鼠的实验研究

李丹;杜德兵;邱绍勤;余平;罗世珍;袁容静;陈冬云   

  1. 湖北宜昌市第三人民医院 宜昌 443003
  • 出版日期:2008-06-10 发布日期:2011-11-03
  • 基金资助:

    宜昌市科技攻关项目(A2007302-30)

Immunotherapeutic effects of IFN-γ combined with M.vaccae vaccine on mice model with tuberculosis

Li Dan,Du Debing,Qiu Shaoqin,et al.   

  1. Department of Respiratory,The third people’s Hospital of Yi Chang,Yi Chang 443003,China
  • Online:2008-06-10 Published:2011-11-03

摘要: 目的研究γ-干扰素联合微卡对结核分枝杆菌感染小鼠的免疫治疗作用及其免疫学机制。方法60只BALB/c小鼠用随机数字表法随机分为正常组、模型组、γ-干扰素组、微卡组及联合组,每组12只。除正常组不造模外,其余4组小鼠经尾静脉注射结核分枝杆菌(H37Rv,106个菌/只)。微卡组于攻毒后10 d腹腔内注射微卡22.5μg/只。γ-干扰素组攻毒后10天腹腔注射γ-干扰素(1万U/只,1次/d)5 d,间隔2 d,继续腹腔注射5 d。联合组2者均注射。感染6周后处死30只小鼠(每组6只),称取小鼠体质量和肺脏及脾脏质量。取肺、脾组织进行结核菌培养和菌落计数,观察肺脏病理改变,同时用ELISA法检测血清IFN-γ、IL-4水平和用RT-PCR法测定肺组织IFN-γmRNAI、L-4 mRNA的表达。其余30只小鼠观察60 d,计算其存活时间。结果模型组肺组织病理改变以渗出为主,病变广泛,增生改变不明显;3个用药组病变范围局限,并可见类上皮细胞、纤维母细胞。模型组观察期结束无一小鼠存活;正常组和联合组在观察期内无一死亡,γ-干扰素组和微卡组在观察期内仅有1只小鼠死亡。感染后6周,γ-干扰素组肺脾菌荷量(×106CFU/g-x±s)(分别为7.12±0.51,6.42±0.48)和微卡组(分别为(6.31±0.47),(6.07±0.39))较模型组(分别为26.18±0.96,18.43±0.85)明显减少(P<0.05),与γ-干扰素组、微卡组比较,联合组肺脾菌荷量为(分别为2.67±0.36,2.12±0.33)减少更显著(P<0.05)。模型组小鼠血清IFN-γ的表达和肺组织IFN-γmRNA(分别为(162±46)pg/ml,(0.18±0.06))的表达较正常组(分别为(521±198)pg/ml,(0.98±0.13))均显著降低(P<0.01),模型组小鼠血清IL-4的表达和肺组织IL-4 mRNA(分别为(102±24.8)pg/ml,(1.46±0.25))的表达较正常组(分别为(56.2±14.5)pg/ml,(0.04±0.01))均显著增高(P<0.01)。γ-干扰素组小鼠血清IFN-γ的表达和肺组织IFN-γmRNA的表达(分别为(402±134)pg/ml,(0.66±0.08))和微卡组(分别为(416±153)pg/ml,(0.68±0.09))均显著高于模型组(P<0.05);与γ-干扰素组、微卡组比较,联合组(分别为(493±145)pg/ml,(0.81±0.11))增高更显著(P<0.05)。γ-干扰素组小鼠血清IL-4的表达和肺组织IL-4 mRNA的表达(分别为(73.5±15.3)pg/ml,(0.63±0.12))和微卡组(分别为(71.3±14.6)pg/ml,(0.59±0.13))均显著低于模型组(P<0.05);与γ-干扰素组、微卡组比较,联合组(分别为(60.8±12.7)pg/ml,(0.28±0.03))降低更显著(P<0.05)。结论γ-干扰素和微卡可减少结核病小鼠肺和脾脏结核菌数量,并增强Th1型免疫反应,抑制Th2型免疫反应,增强小鼠抵抗结核分枝菌感染的能力,且两者联用具有协同作用。

关键词: &gamma, -干扰素, 微卡, 分枝杆菌, 结核, 细胞因子

Abstract: Objective To study the immunotherapeutic effects and its mechanism of IFN-γ combined with M.vaccae vaccine on mice model with tuberculosis.Methods Sixty BALB/c mice were randomly divided into 5 groups: normal group,tuberculosis model group,IFN-γ group,M.vaccae vaccine group,the IFN-γ+ M.vaccae vaccine group.Each group included 12 mice.Forty-eight mice was infected by the tail vein with 1×106CFU of M.tuberculosis H37Rv strain,and treated intraperitoneally with the saline,IFN-γ,IFN-γ combined with M.vaccae vaccine at 10 days after infection.Six mice each group were sacrificed at 6 weeks after infection.The body weights of the mice and the weights of lungs and spleens from the mice were measured.The lungs and spleens of the mice were taken,determined the CFU,and observed histopathologic changes.The level of IFN-γ and IL-4 in the blood were detected with ELISA method.The expression of IFN-γ mRNA and IL-4 mRNA in lungs were detected by RT-PCR method.The survival times in the other 30 mice were evaluated in 60 days.Results The pathological changes of lungs in the three treatment groups were localized,while those in tuberculosis model group were extensive.All of mice died in tuberculosis model group,none of mice died in the normal group and the IFN-γ+ M.vaccae vaccine group,only one mice died in IFN-γ group and M.vaccae vaccine group.At 6 weeks after infection,compared with tuberculosis model group,the CFUs in lungs and spleens were significantly decreased in IFN-γ groups(7.12±0.51) and(6.42±0.48) and in M.vaccae vaccine groups(6.31±0.47) and(6.07±0.39),particularly in the IFN-γ+ M.vaccae vaccine group(2.67±0.36) and(2.12±0.33)(P<0.05).The level of IFN-γ in the blood and the expression of IFN-γ mRNA in lung tissue of mice in tuberculosis model group(162±46) pg/ml and(0.18±0.06) were lower than that in normal group((521±198) pg/ml and(0.98±0.13))(P<0.01),and IFN-γ groups(402±134) pg/ml and(0.66±0.08),M.vaccae vaccine groups(416±153) pg/ml and(0.68±0.09) and IFN-γ+ M.vaccae vaccine group(493±145) pg/ml,(0.81±0.11) were higher than that in tuberculosis model group(P<0.05).The level of IL-4 in the blood and the expression of IL-4 mRNA in lung tissue in tuberculosis model group((102±24.8) pg/ml and(1.46±0.25))were higher than that in normal group((56.2±14.5) pg/ml and(0.04±0.01))(P<0.01),and IFN-γ groups((73.5±15.3) pg/ml and(0.63±0.12)),M.vaccae vaccine groups(71.3±14.6) pg/ml and(0.59±0.13) and IFN-γ+ M.vaccae vaccine group(60.8±12.7) pg/ml and(0.28±0.03) were lower than that in tuberculosis model group(P<0.05).Conclusions IFN-γ combined with M.vaccae vaccine could improve host defence against the infection of Mycobacterium tuberculosis,and reduce mycobacterial growth during tuberculosis,and might be associated with a decrease in inflammation in lung and spleen tissue by activating the Th1 response,and inhibiting the Th2 response,and they have cooperative effect.

Key words: interferon-&gamma, M.vaccae, mycobacterium, tuberculosis, cytokines