一株94 KD高分子量屋尘螨变应原的纯化及特性研究。

J J Wey, H F Lee, T H Chang, C C Chou, K H Hsieh, J H Huang
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摘要

在许多国家,屋尘螨致敏原是引起严重过敏性哮喘和鼻炎的重要原因。虽然一些低到中等分子量的过敏原已经被很好地表征,但对高分子量ige结合成分的研究报道有限。本研究从翼蝶螨体粗提取物中纯化了一个分子量为94 kD的高分子量变应原,并对其进行了表征。采用单克隆抗体亲和层析和高效液相层析对94kd过敏原进行纯化。体外和体内实验证实了其抗原性和致敏性。制备了针对翼龙骨窦94 kD高分子量组分的2205-3.45和2220-7.25单抗。这些单克隆抗体识别的表位具有物种特异性。酶联免疫吸附法(ELISA)检测40例翼蝶蝶过敏哮喘患儿血清IgE反应性,37.5%患儿光密度值(0.011 ~ 0.452)明显高于正常儿童(0.013 ~ 0.035)。在体皮肤试验中,20例哮喘患儿94 kD过敏原阳性9例(45%)。结果表明,94kd高分子量成分是台湾地区屋尘螨体内存在的重要变应原。
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Purification and characterization of a 94 KD high molecular weight allergen from house dust mite, Dermatophagoides pteronyssinus.

House dust mite allergens from Dermatophagoides pteronyssinus is an important cause of severe allergic asthma and rhinitis in many countries. Although several low to medium molecular weight allergens had been well characterized, limited studies on the high molecular weight IgE-binding components were reported. In this study, a 94 kD high molecular weight allergen from crude mite body extract of D. pteronyssinus was purified and characterized. Monoclonal antibody (mAb) affinity chromatography and high performance liquid chromatography were used to purify 94 kD allergen. Its antigenicity and allergenicity were confirmed by in vitro and in vivo studies. Two mAbs 2205-3.45 and 2220-7.25 specific to 94 kD high molecular weight component of D. pteronyssinus were generated. The epitopes recognized by these mAbs were species-specific. Enzyme-linked immunosorbent assay (ELISA) of IgE reactivity in the sera from 40 asthmatic children allergic to D. pteronyssinus showed that 37.5% of them had significantly higher optical density values (range 0.011 to 0.452) than normal (range 0.013 to 0.035). In in vivo skin test showed that 9 out of 20 (45%) asthmatic children were positive to 94 kD allergen. The results demonstrate that 94 kD high molecular weight component is an important allergen existing in house dust mite in Taiwan.

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Studies on the serological cross-reaction between dengue and Japanese encephalitis. Evaluation of CLO test and polymerase chain reaction for biopsy-dependent diagnosis of Helicobacter pylori infection. Purification and characterization of a 94 KD high molecular weight allergen from house dust mite, Dermatophagoides pteronyssinus. Population cell differentiation of Serratia marcescens on agar surface and in broth culture. [Detection of neutralizing antibodies to Japanese encephalitis virus by enzyme-linked immunosorbent assay (ELISA)].
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