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首页> 外文期刊>Chinese Medical Journal >DNA vaccine encoding Der p 2 allergen generates immunologic protection in recombinant Der p 2 allergen-induced allergic airway inflammation mice model
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DNA vaccine encoding Der p 2 allergen generates immunologic protection in recombinant Der p 2 allergen-induced allergic airway inflammation mice model

机译:编码Der p 2过敏原的DNA疫苗在重组Der p 2过敏原诱导的过敏性气道炎症小鼠模型中产生免疫保护

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Background DNA immunization is a promising novel type of immunotherapy against allergy. An estimated 79. 2% patients with asthma, wheezing and/or rhinitis suffer from Dermatophagoides pteronyssinus group 2 (Der p 2) allegen. The aim of the present study was to determine whether DNA vaccine encoding Der p 2 could generate immunologic protection in recombinant Der p 2 ( rDer p 2 ) allergen-induced allergic airway inflammation mice model and to understand the role of DNA vaccination in specific-allergen immunotherapy for asthma. Methods After DNA vaccination, BALB/c mice were sensitized by intraperitoneal injection ( i. p) and challenged by intranasal instillation of rDer p 2. The lung tissues were assessed using hematoxylin and eosin. Mucus-producing goblet cells were identifed using periodic acid-Schiff( PAS ) /alcian blue. The total cell number and composition of bronchoalveolar lavage samples were determined. The levels of the cytokines IL-4 and IFN-γ, as well as IgE and IgG_(2a) in the serum were determined by enzyme-linked immunosorbent assay. Allergen-specific IL-4 and IFN-γ production by spleen cells were also measured by enzyme-linked immunosorbent assay. Expression of signal transducer and activator of transcription 6 ( STAT6) in splenocytes were determined by Western blot. Results DNA vaccine encoding Der p 2 allergen inhibited extensive infiltration of inflammatory cells and production of mucin induced by allergen. The influx of eosinophils into the lung interstitium was significantly reduced after administration of DNA vaccine. Significant reductions of IL-4 and increase in levels of IFN-γ in bronchoalveolar lavage fluid were observed. The allergen-specific IgE was markedly decreased in mice receiving DNA vaccination. Allergen could induce higher IFN-γ, weaker IL-4 in cultured spleen cells from mice receiving DNA vaccine. DNA vaccination inhibited STAT6 expression of spleen cells induced by allergen. Conclusion These results indicated that DNA vaccine encoding Der p 2 allergen generates immunologic protection in recombinant Der p 2 allergen-induced allergic airway inflammation mice model with regulating the immune response towards a Th1-type reaction.
机译:背景技术DNA免疫是一种抗过敏的新型免疫疗法。估计有79. 2%的哮喘,喘息和/或鼻炎患者患有Dermatophagoides pteronyssinus组2(Der p 2)过敏原。本研究的目的是确定编码Der p 2的DNA疫苗能否在重组Der p 2(rDer p 2)过敏原诱导的过敏性气道炎症小鼠模型中产生免疫保护作用,并了解DNA疫苗在特异性过敏原中的作用。哮喘的免疫疗法。方法DNA疫苗接种后,通过腹膜内注射(i。p)致敏BALB / c小鼠,并通过鼻内滴注rDer p 2激发小鼠。用苏木精和曙红评估肺组织。使用高碘酸-席夫(PAS)/阿尔辛蓝鉴定产生粘液的杯状细胞。测定了支气管肺泡灌洗样品的总细胞数和组成。通过酶联免疫吸附试验测定血清中细胞因子IL-4和IFN-γ的水平,以及IgE和IgG_(2a)的水平。还通过酶联免疫吸附测定法测量了脾细胞产生的变应原特异性IL-4和IFN-γ。通过蛋白质印迹法测定脾细胞中信号转导子和转录激活子6(STAT6)的表达。结果编码Der p 2变应原的DNA疫苗可抑制炎症细胞的广泛浸润和变应原诱导的粘蛋白产生。给予DNA疫苗后,嗜酸性粒细胞向肺间质的流入明显减少。观察到支气管肺泡灌洗液中IL-4显着降低和IFN-γ水平升高。接受DNA疫苗接种的小鼠的变应原特异性IgE明显降低。过敏原可以在接受DNA疫苗的小鼠的脾脏细胞中诱导更高的IFN-γ和更弱的IL-4。 DNA疫苗可抑制变应原诱导的脾细胞STAT6表达。结论这些结果表明,编码Der p 2过敏原的DNA疫苗在重组Der p 2过敏原诱导的过敏性气道炎症小鼠模型中产生免疫保护,并调节针对Th1型反应的免疫应答。

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