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机构地区:[1]第四军医大学附属西京医院呼吸与危重症医学科,陕西西安710032 [2]第四军医大学附属西京医院放疗科,陕西西安710032 [3]第四军医大学附属西京医院检验科,陕西西安710032
出 处:《现代生物医学进展》2013年第8期1435-1438,1477,共5页Progress in Modern Biomedicine
基 金:国家自然科学基金项目(30871114)
摘 要:目的:Th1与Th2的平衡紊乱是过敏性哮喘的免疫学基础,本研究通过给予小鼠口服免疫不同亲和力屋尘螨抗原Der p2重组耻垢分枝杆菌,来比较其调节免疫应答的差异。方法:1,分别给予6-8周BALB/c小鼠口服接种Mycobacterium Smegmatis(M.S)、pCW-Der p2-rM.S及pCW-Der p2-PEB1-rM.S,在末次免疫后第14、28、56天分别用夹心ELISA法测定小鼠血清及脾脏淋巴细胞培养上清中IFN-γ、IL-2及IL-4的含量。结果:夹心ELISA结果显示,无论是血清还是脾脏淋巴细胞培养上清中,各组IFN-γ、IL-2水平逐渐升高,IL-4水平逐渐降低,8周时更明显,pCW-Der p2-PEB1-rM.S组与M.S、pCW-Der p2-rM.S组相比有明显统计学差异。体外给予Der p2蛋白刺激后,pCW-Der p2-rM.S及pCW-Der p2-PEB1-rM.S组变化更加明显,而M.S组无明显变化。结论:小鼠口服免疫pCW-Der p2-PEB1-rM.S能明显提高Th1型免疫反应,与pCW-Der p2-rM.S组相比有统计学学差异。三种不同亲和力重组耻垢分枝杆菌经口服后均能诱导小鼠产生Th1型免疫应答,且pCW-Der p2-rM.S及pCW-Der p2-PEB1-rM.S诱导产生的Th1优势应答具有Der p2抗原特异性。本研究弥补了粘膜型疫苗低亲和力的不足,为新型口服疫苗的制备和改进创造了条件。Objective: Thl and Th2 balance disorder is the basic immunology of allergic asthma. In this study, we mainly investigate the immune response differences for BALB/c mice with oral administrated different affinity of Mycobacterium Smegmatis. Methods: Mice were killed at 14,28,56 days after intragastric administrated different affinity of Mycobacterium Smegmatis, measured serum and spleen lymphocyte culture supematant by ELISA, respectively. Results: The ELISA showed that with the growth of time, IFN-γ and IL-2 were gradually increased, IL-4 were gradually decreased. All the change reached the peak on the 56th day (P〈 0.05). The groups of pCW-Der p2-PEBI-rM.S and pCW-Der p2-rM.S showed significant difference compared with M.S. group (P〈 0.05), after stimulating with Der p2 protein, more obvious change could be observed in the two groups. Conclusion: All groups of Mycobacterium Smegmatis took orally could induce Thl-type immune response, and the response produced by pCW-Der p2-PEBI-rM.S and pCW-Der p2-rM.S was the specific response to Der p2. There showed a significant difference for pCW-Der p2-PEBI-rM.S compared with pCW-Der p2-rM.S group (P〈 0.05). This study to make up for a insufficiency of mucosal vaccine with low affinity, and create a conditions for new oral vaccine construction and improvement.
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