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首页> 外文期刊>The Journal of Immunology: Official Journal of the American Association of Immunologists >A combination vaccine for allergy and rhinovirus infections based on rhinovirus-derived surface protein VP1 and a nonallergenic peptide of the major timothy grass pollen allergen Phl p 1.
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A combination vaccine for allergy and rhinovirus infections based on rhinovirus-derived surface protein VP1 and a nonallergenic peptide of the major timothy grass pollen allergen Phl p 1.

机译:基于鼻病毒衍生的表面蛋白VP1和主要的提摩西草花粉过敏原Phl p 1的非过敏原肽的变应性和鼻病毒感染的联合疫苗。

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摘要

Allergens and rhinovirus infections are among the most common elicitors of respiratory diseases. We report the construction of a recombinant combination vaccine for allergy and rhinovirus infections based on rhinovirus-derived VP1, the surface protein which is critically involved in infection of respiratory cells, and a nonallergenic peptide of the major grass pollen allergen Phl p 1. Recombinant hybrid molecules consisting of VP1 and a Phl p 1-derived peptide of 31 aa were expressed in Escherichia coli. The hybrid molecules did not react with IgE Abs from grass pollen allergic patients and lacked allergenic activity when exposed to basophils from allergic patients. Upon immunization of mice and rabbits, the hybrids did not sensitize against Phl p 1 but induced protective IgG Abs that cross-reacted with group 1 allergens from different grass species and blocked allergic patients' IgE reactivity to Phl p 1 as well as Phl p 1-induced basophil degranulation. Moreover, hybrid-induced IgG Abs inhibited rhinovirus infection of cultured human epithelial cells. The principle of fusing nonallergenic allergen-derived peptides onto viral carrier proteins may be used for the engineering of safe allergy vaccines which also protect against viral infections.
机译:过敏原和鼻病毒感染是呼吸系统疾病的最常见诱因。我们报告了基于鼻病毒衍生的VP1,主要参与呼吸道细胞感染的表面蛋白以及主要草花粉过敏原Phl p 1的非过敏原肽的重组用于过敏和鼻病毒感染的重组联合疫苗的构建。在大肠杆菌中表达由VP1和31位氨基酸的Phl p 1衍生肽组成的分子。杂种分子与草花粉过敏患者的IgE Abs不反应,并且暴露于过敏患者的嗜碱性粒细胞时缺乏过敏原活性。小鼠和兔子免疫后,杂种对Phl p 1不敏感,但诱导了保护性IgG Abs,该抗体与来自不同草种的第1组变应原交叉反应,并阻断了过敏患者对Phl p 1和Phl p 1的IgE反应性。诱导的嗜碱性粒细胞脱粒。此外,杂交体诱导的IgG Abs抑制了培养的人上皮细胞的鼻病毒感染。将非变应原性变应原衍生的肽融合到病毒载体蛋白上的原理可用于工程化安全变态反应疫苗,该疫苗还可以防止病毒感染。

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