[自身免疫性疾病患者血清对由蛔虫过敏原 T 表位构建的多表位蛋白的 IgE 反应性]。

Luis Fang, Dalgys Martínez, Catherine Meza-Torres, Ana Moreno-Woo, Nicole Pereira-Sanandres, Alex Domínguez-Vargas, Gloria Garavito, Eduardo Egea
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引用次数: 0

摘要

目的评估 1 型糖尿病 (T1D)、狼疮性肾炎 (LN) 和幼年特发性关节炎 (JIA) 患者血清中 IgE 对由 A. lumbricoides 过敏原 T 表位构建的分子的反应性:方法:我们设计并表达了一种人工合成的多表位蛋白,命名为MP1。通过间接 ELISA 法,我们评估了 45 名患有狼疮性肾炎(LN;n=25)、1 型糖尿病(T1D;n=10)和幼年特发性关节炎(JIA;n=10)的哥伦比亚加勒比海患者血清中对 MP1 和蛔虫全身提取物的 IgE 反应性。患有多种自身免疫疾病的患者不包括在内。所有患者均由其专科医生转介至本研究:JIA患者的IgE中位数为484.2纳克/毫升(IQR:203.4),LN患者为325.6纳克/毫升(IQR:179.3),T1D组为424.7纳克/毫升(IQR:80.1)。另一方面,JIA 患者对 MP1 的 IgE 反应性为 126.4 纳克/毫升(IQR:90.9),LN 患者为 130.7 纳克/毫升(IQR:94.8),T1D 组为 148.8 纳克/毫升(IQR:102.1)。虽然患者组之间没有统计学差异,但与蛔虫提取物(IgE 中位数:380.7 ng/ml;IQR:175.8)相比,所有患者(n:45)对 MP1 的 IgE(IgE 中位数:134.2 ng/ml;IQR:100)显著降低;(W:0.732;P 值:1.034x10-7):这些初步结果表明,与蛔虫提取物相比,MP1 在自身免疫性疾病患者中显示出低 IgE 反应性的抗原特性。要更好地了解该分子诱导的免疫反应,还需要进一步研究。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[IgE reactivity of sera from patients with autoimmune diseases against a multi-epitope protein constructed from T epitopes of Ascaris lumbricoides allergens].

Objective: To evaluate the IgE reactivity of sera in patients suffering from type 1 diabetes (T1D), lupus nephritis (LN) and juvenile idiopathic arthritis (JIA) against a molecule constructed from T epitopes of A. lumbricoides allergens.

Methods: We designed and expressed a synthetic multi-epítope protein named MP1 from A. lumbricoides and house dust mites allergens. By indirect ELISA, we evaluated IgE-reactivity to MP1 and to the whole-body extract of Ascaris lumbricoides in 45 sera from Colombian Caribbean patients with lupus nephritis (LN; n=25), type 1 diabetes (T1D; n=10) and Juvenil idiopathic arthritis (JIA; n=10). Individuals with poly autoimmunity were excluded. All patients were referred to the study by their specialist doctor.

Results: IgE to whole-body extract of A. lumbricoides showed the following median concentrations.

484.2 ng/ml (IQR: 203.4) in JIA patients, 325.6 ng/ml (IQR: 179.3) in individuals with LN, and 424.7 ng/ml (IQR: 80.1) in the T1D group. On the other hand, IgE-reactivity to MP1 was 126.4 ng/ml (IQR: 90.9) in JIA patients, 130.7 ng/ml (IQR: 94.8) in an individual with LN, and 148.8 ng/ml (IQR: 102.1) in the T1D group. Although no statistical differences were observed between patient groups, the IgE to MP1 in all patients (n: 45) (IgE median: 134.2 ng/ml; IQR: 100) were significantly less compared to Ascaris extract (IgE median: 380.7 ng/ml; IQR: 175.8); (W: 0.732; p-value: 1.034x10-7).

Conclusions: These preliminary results suggest that MP1 showed antigenic properties with low IgE- reactivity, compared to Ascaris lumbricoides extracted in individuals with autoimmune diseases. Further studies are needed to understand better the immune response induced by this molecule.

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