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High serum tryptophan concentration in pollinosis patients is associated with unresponsiveness to pollen extract therapy.

机译:花粉症患者的血清色氨酸浓度高与对花粉提取物疗法无反应有关。

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BACKGROUND/AIMS: The immunologic background of allergic asthma and rhinitis includes a preponderance of Th2-type immunity. In parallel, Th1-type immune response is suppressed by Th2-type cytokines. As a consequence, biochemical pathways triggered by Th1-type cytokine interferon-gamma, such as tryptophan degradation by indoleamine 2,3-dioxygenase and neopterin production, might be altered. We examined whether they are related to the outcome of hyposensitization therapy in atopic patients. METHODS: In serum specimens of 44 atopic patients (18 women, 26 men) before any specific immunotherapy, tryptophan and kynurenine concentrations were measured by HPLC, and the kynurenine to tryptophan ratio (kyn/trp) was calculated. Neopterin concentrations were measured by ELISA. Results were compared with concentrations in 38 serum specimens from healthy blood donors and with the outcome of specific subcutaneous immunotherapy in atopics: on clinical grounds, 27 patients were classified as responders, and 17 patients as non-responders. RESULTS: Serum tryptophan concentrations were higher in atopics (84.3 +/- 24.4 microM) than in blood donors (57.9 +/- 7.46 microM; p < 0.001), kynurenine and kyn/trp were not different between the 2 groups. All of the neopterin concentrations measured in patients were <8.7 nM, the upper limit of the normal. Non-responders to subcutaneous immunotherapy had significantly higher tryptophan concentrations (95.7 +/- 27.0 microM) than responders (77.1 +/- 19.9 microM; p = 0.01). No other marker concentrations differed between the groups. CONCLUSIONS: The measurement of serum tryptophan may present an option to predict the outcome of pollen extract therapy. Higher tryptophan levels may result from lower indoleamine 2,3-dioxygenase activity in atopics. However, this possible relationship needs to be confirmed in further studies.
机译:背景/目的:过敏性哮喘和鼻炎的免疫学背景包括大量的Th2型免疫。同时,Th2型细胞因子抑制Th1型免疫反应。结果,可能会改变由Th1型细胞因子干扰素-γ触发的生化途径,例如吲哚胺2,3-双加氧酶和新蝶呤产生的色氨酸降解。我们检查了它们是否与特应性患者低敏治疗的结果有关。方法:在进行任何特异性免疫治疗之前,对44位特应性患者(18名女性,26名男性)的血清样本进行HPLC测定色氨酸和犬尿氨酸的浓度,并计算犬尿氨酸与色氨酸的比率(kyn / trp)。通过ELISA测量新蝶呤浓度。将结果与健康献血者的38个血清样本中的浓度以及特应性皮下特异性皮下免疫疗法的结果进行了比较:根据临床理由,将27例患者归为有反应者,将17例患者归为无反应者。结果:异位症患者的血清色氨酸浓度(84.3 +/- 24.4 microM)高于献血者(57.9 +/- 7.46 microM; p <0.001),犬尿氨酸和kyn / trp在两组之间没有差异。在患者中测得的所有新蝶呤浓度均<8.7 nM,为正常上限。皮下免疫治疗无反应者的色氨酸浓度(95.7 +/- 27.0 microM)明显高于反应者(77.1 +/- 19.9 microM; p = 0.01)。两组之间其他标志物浓度无差异。结论:血清色氨酸的测定可能为预测花粉提取物治疗的结果提供了一种选择。异位症中较低的吲哚胺2,3-二加氧酶活性可能导致较高的色氨酸水平。但是,这种可能的关系有待进一步研究证实。

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