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首页> 外文期刊>Brazilian Journal of Medical and Biological Research >IgE cross-reactivity between Lolium multiflorum and commercial grass pollen allergen extracts in Brazilian patients with pollinosis
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IgE cross-reactivity between Lolium multiflorum and commercial grass pollen allergen extracts in Brazilian patients with pollinosis

机译:多花黑麦草与商业草粉花粉过敏原提取物在巴西花粉病患者中的IgE交叉反应

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Lolium multiflorum (Lm) grass pollen is the major cause of pollinosis in Southern Brazil. The objectives of this study were to investigate immunodominant components of Lm pollen allergens and the cross-reactivity of IgE with commercial grass pollen allergen extracts. Thirty-eight serum samples from patients with seasonal allergic rhinitis (SAR), 35 serum samples from patients with perennial allergic rhinitis (PAR) and 30 serum samples from non-atopic subjects were analyzed. Allergen sensitization was evaluated using skin prick test and serum IgE levels against Lm pollen extract were determined by ELISA. Inhibition ELISA and immunoblot were used to evaluate the cross-reactivity of IgE between allergens from Lm and commercial grass pollen extracts, including L. perenne (Lp), grass mix I (GI) and II (GII) extracts. IgE antibodies against Lm were detected in 100% of SAR patients and 8.6% of PAR patients. Inhibition ELISA demonstrated IgE cross-reactivity between homologous (Lm) and heterologous (Lp or GII) grass pollen extracts, but not for the GI extract. Fifteen IgE-binding Lm components were detected and immunoblot bands of 26, 28-30, and 32-35 kDa showed >90% recognition. Lm, Lp and GII extracts significantly inhibited IgE binding to the most immunodominant Lm components, particularly the 55 kDa band. The 26 kDa and 90-114 kDa bands presented the lowest amount of heterologous inhibition. We demonstrated that Lm extract contains both Lm-specific and cross-reactive IgE-binding components and therefore it is suitable for measuring quantitative IgE levels for diagnostic and therapeutic purposes in patients with pollinosis sensitized to Lm grass pollen rather than other phylogenetically related grass pollen extracts.
机译:多花黑麦草(Lm)草花粉是巴西南部花粉病的主要原因。这项研究的目的是调查Lm花粉过敏原的免疫优势成分和IgE与商业草粉花粉过敏原提取物的交叉反应性。分析了季节性过敏性鼻炎(SAR)患者的38份血清样本,多年生过敏性鼻炎(PAR)患者的35份血清样本和非特应性受试者的30份血清样本。使用皮肤点刺试验评估变应原的致敏性,并通过ELISA测定针对Lm花粉提取物的血清IgE水平。抑制酶联免疫吸附测定(ELISA)和免疫印迹法用于评估Lm和商业草粉花粉提取物(包括紫苏乳杆菌(Lp),混合I(GI)和II(GII)提取物)的过敏原之间IgE的交叉反应性。在100%的SAR患者和8.6%的PAR患者中检测到针对Lm的IgE抗体。抑制ELISA证明了同源(Lm)和异源(Lp或GII)草花粉提取物之间的IgE交叉反应,但对GI提取物却没有。检测到15个IgE结合Lm成分,并且26、28-30和32-35 kDa的免疫印迹带显示> 90%的识别率。 Lm,Lp和GII提取物可显着抑制IgE与免疫力最强的Lm成分(特别是55 kDa条带)的结合。 26 kDa和90-114 kDa的条带显示出最低的异源抑制量。我们证明了Lm提取物同时包含Lm特异性和交叉反应性IgE结合成分,因此它适用于测量对Lm草花粉致敏的花粉病患者的诊断和治疗目的定量IgE水平,而不是其他与系统发育相关的草花粉提取物。

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