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首页> 外文期刊>Clinical and experimental allergy : >Hypoallergenic mutants of Ole e 1, the major olive pollen allergen, as candidates for allergy vaccines.
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Hypoallergenic mutants of Ole e 1, the major olive pollen allergen, as candidates for allergy vaccines.

机译:Ole e 1的低变应原突变体,主要的橄榄花粉变应原,作为过敏疫苗的候选者。

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摘要

BACKGROUND: The C-terminal region of Ole e 1, a major allergen from olive pollen, is a dominant IgE-reactive site and offers a target for site-directed mutagenesis to produce variants with reduced IgE-binding capability. OBJECTIVE: To evaluate in vitro and in vivo the immunogenic properties of three engineered derivatives of Ole e 1. METHODS: One point (Y141A) and two deletion (135Delta10 and 140Delta5) mutants were generated by site-directed mutagenesis of Ole e 1-specific cDNA and produced in Pichia pastoris. Ole e 1 mutants were analysed for IgE reactivity by ELISA using sera from olive pollen-allergic patients. Their allergenicity was also investigated in both a mouse model of allergic sensitization and in basophil activation assays. IgG1 response was assayed by immunoblotting and competitive ELISA. T cell reactivity was evaluated by proliferation assays and cytokine production in splenocyte cultures. RESULTS: The 135Delta10 mutant showed the strongest reduction in the IgE-binding capability of sera from olive pollen-allergic patients. Rat basophil leukaemia assays identified the deletion mutant 135Delta10 as the variant with the lowest beta-hexosaminidase-releasing capacity. Furthermore, the same 135Delta10 mutant induced the lowest IgE levels in a BALB/c mouse model of sensitization. All Ole e 1 mutants retained their allergen-specific T cell reactivity. Immunization of mice with the mutants induced IgG1 antibodies, which cross-reacted with Ole e 1 and Ole e 1-like allergens from ash, lilac and privet pollens. The ability of the human IgE to block the binding of anti-Ole e 1 mutant-specific mouse IgG1 antibodies to natural Ole e 1 demonstrated that Ole e 1 mutants are able to induce in vivo antibodies reactive to the natural allergen. CONCLUSION: The 135Delta10 mutant with reduced allergenicity, intact T cell reactivity and capacity to induce blocking antibodies could provide a suitable candidate vaccine for efficient and safer therapy of olive pollen allergy.
机译:背景:来自橄榄花粉的主要变应原Ole e 1的C端区域是主要的IgE反应位点,为定点诱变提供目标,以产生具有降低的IgE结合能力的变体。目的:评价三种Ole e 1工程衍生物的免疫原性。方法:通过定点诱变Ole e 1特异性位点产生一个点(Y141A)和两个缺失(135Delta10和140Delta5)突变体。 cDNA,在巴斯德毕赤酵母中产生。使用来自橄榄花粉过敏患者的血清,通过ELISA分析Ole e 1突变体的IgE反应性。还在变态反应致敏的小鼠模型和嗜碱性粒细胞活化试验中研究了它们的致敏性。 IgG1反应通过免疫印迹和竞争性ELISA进行测定。通过增殖测定和脾细胞培养物中细胞因子的产生来评估T细胞反应性。结果:135Delta10突变体显示来自花粉过敏患者的血清中IgE结合能力的降低最大。大鼠嗜碱性粒细胞白血病试验鉴定出缺失突变体135Delta10是具有最低的β-己糖胺酶释放能力的变异体。此外,相同的135Delta10突变体在致敏的BALB / c小鼠模型中诱导出最低的IgE水平。所有的Ole e 1突变体均保留了其变应原特异性T细胞反应性。用突变体免疫小鼠可诱导产生IgG1抗体,该抗体与来自灰分,丁香和女贞花粉的Ole e 1和Ole e 1样过敏原交叉反应。人IgE阻断抗Ole e 1突变体特异性小鼠IgG1抗体与天然Ole e 1结合的能力证明,Ole e 1突变体能够诱导对天然过敏原具有反应性的体内抗体。结论:具有降低的致敏性,完整的T细胞反应性和诱导阻断抗体能力的135Delta10突变体可以为有效且安全地治疗橄榄花粉过敏提供合适的候选疫苗。

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