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DNA疫苗对小鼠模型中变应原诱导的过敏性气道炎症的治疗作用。

Therapeutic effects of DNA vaccine on allergen-induced allergic airway inflammation in mouse model.

作者信息

Li Guoping, Liu Zhigang, Zhong Nanshan, Liao Bin, Xiong Ying

机构信息

Inflammation and Allergic Diseases Research Unit, Affiliated Hospital of Luzhou Medical College, Luzhou 646000, Sichuan, China.

出版信息

Cell Mol Immunol. 2006 Oct;3(5):379-84.

Abstract

Vaccination with DNA encoding Dermatophagoides pteronyssinus group 2 (Der p 2) allergen previously showed its effects of immunologic protection on Der p 2 allergen-induced allergic airway inflammation in mice. In present study, we investigated whether DNA vaccine encoding Der p 2 could exert therapeutic role on allergen-induced allergic airway inflammation in mouse model and explored the mechanism of DNA vaccination in asthma specific-allergen immunotherapy. After sensitized and challenged by Der p 2, the BALB/c mice were immunized with DNA vaccine. The degrees of cellular infiltration were scored. IgE levels in serum and IL-4/IL-13 levels in BALF were determined by ELISA. The lung tissues were assessed by histological examinations. Expressions of STAT6 and NF-kappaB in lung were determined by immunohistochemistry staining. Vaccination of mice with DNA vaccine inhibited the development of airway inflammation and the production of mucin induced by allergen, and reduced the level of Der p 2-specific IgE level. Significant reductions of eosinophil infiltration and levels of IL-4 and IL-13 in BALF were observed after vaccination. Further more, DNA vaccination inhibited STAT6 and NF-kappaB expression in lung tissue in Der p 2-immunized mice. These results indicated that DNA vaccine encoding Der p 2 allergen could be used for therapy of allergen-induced allergic airway inflammation in our mouse model.

摘要

先前用编码屋尘螨第2组(Der p 2)变应原的DNA进行疫苗接种,已显示其对Der p 2变应原诱导的小鼠过敏性气道炎症具有免疫保护作用。在本研究中,我们调查了编码Der p 2的DNA疫苗是否能对小鼠模型中变应原诱导的过敏性气道炎症发挥治疗作用,并探讨了DNA疫苗接种在哮喘特异性变应原免疫治疗中的机制。用Der p 2致敏并激发后,用DNA疫苗对BALB/c小鼠进行免疫接种。对细胞浸润程度进行评分。通过ELISA测定血清中的IgE水平和BALF中的IL-4/IL-13水平。通过组织学检查评估肺组织。通过免疫组织化学染色测定肺中STAT6和NF-κB的表达。用DNA疫苗对小鼠进行接种可抑制变应原诱导的气道炎症发展和粘蛋白产生,并降低Der p 2特异性IgE水平。接种后观察到BALF中嗜酸性粒细胞浸润以及IL-4和IL-13水平显著降低。此外,DNA疫苗接种抑制了Der p 2免疫小鼠肺组织中STAT6和NF-κB的表达。这些结果表明,编码Der p 2变应原的DNA疫苗可用于治疗我们小鼠模型中变应原诱导的过敏性气道炎症。

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