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首页> 外文期刊>International Journal of Clinical and Experimental Medicine >Construction of the recombinant vaccine based on T-cell epitope encoding Der p1 and evaluation on its specific immunotherapy efficacy
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Construction of the recombinant vaccine based on T-cell epitope encoding Der p1 and evaluation on its specific immunotherapy efficacy

机译:基于编码Der p1的T细胞表位的重组疫苗的构建及其特异性免疫治疗效果的评价

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摘要

Specific immunotherapy (SIT) is currently recognized as the only etiological therapy to ameliorate asthmatic symptom. The current study was aimed at evaluating the immune effect of vaccine MAT3T designed on MHCII pathway, which includes T cell fusion peptide encoding emDermatophagoides pteronyssinus/em class 1 allergen (Der p1). We initially cloned the nucleotide sequences of TAT, IhC and 3 segments of T cell epitope coding for Der p1, and reassembled these sequences in linear manner to form fusion gene named MAT3T, which was applied to immunize the asthmatic models of mice induced by Der p1 allergen for tentative SIT. ELISA results showed that MAT3T was able to increase the level of IFN-γ in BALF and allergen specific antibody IgGsub2a/sub in serum, while decrease the level of IL-13 in BALF and allergen specific antibody IgE and IgGsub1/sub. Pathological confirmation further revealed that the inflammatory reactions and inflammatory cell infiltration were totally reduced in lung tissue of mice after MAT3T treatment. Our results show that the recombinant allergen MAT3T can effectively correct the imbalance of Th1/Th2, and MAT3T may be used as candidate vaccine against asthma on SIT basis.
机译:目前公认特异性免疫疗法(SIT)是改善哮喘症状的唯一病因疗法。目前的研究旨在评估针对MHCII途径设计的疫苗MAT3T的免疫效果,该途径包括编码 Dermatophagoides pteronyssinus 1类过敏原(Der p1)的T细胞融合肽。我们首先克隆了TAT,IhC和编码Der p1的T细胞表位的3个片段的核苷酸序列,然后以线性方式重组这些序列以形成名为MAT3T的融合基因,并将其用于免疫Der p1诱导的哮喘模型暂时性SIT的过敏原。 ELISA结果表明MAT3T能够提高IFN-γ水平。降低血清中BALF和过敏原特异性抗体IgG 2a 的水平,同时降低BALF和过敏原特异性抗体IgE和IgG 1 的IL-13水平。病理证实进一步显示,MAT3T处理后,小鼠肺组织中的炎症反应和炎症细胞浸润完全减少。我们的结果表明,重组变应原MAT3T可以有效纠正Th1 / Th2的失衡,并且MAT3T可以作为基于SIT的哮喘候选疫苗。

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