扁平苔藓患者血清新蝶呤水平。

Dorota Krasowska, Grazyna Chodorowska, Joanna Bartosińska, Julia Warmińska, Agnieszka Jermak, Anna Kur, Anna Kowal, Jarosław Bogaczewicz
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引用次数: 0

摘要

扁平苔藓(LP)是一种慢性皮肤病,其临床特征包括轻度红斑到紫色平顶多边形丘疹。扁平苔藓的病因尚不清楚,但一直认为免疫机制是重要的。尽管监测免疫介导性疾病的病程具有重要意义,但可用于扁平地衣的可靠生物标志物数量有限。新蝶呤(Neopterin, NP)是一种2-氨基-4-羟基-(1'2'3'-三羟丙基)-蝶啶,由单核细胞和巨噬细胞分泌,主要响应活化的t淋巴细胞分泌inf - γ。因此NP可能是t细胞介导免疫的敏感标记物。本研究的目的是评估扁平苔藓患者的血清新蝶呤水平,并探讨血清新蝶呤水平是否反映了这种疾病的广泛病变和进展。我们研究了66例扁平苔藓患者,他们被分为两个诊断组:第一组包括33例全身性病变患者;II组33例病灶范围明确。对照组由30名性别和年龄匹配的健康个体组成。用市售的酶联免疫吸附测定试剂盒测定血清新蝶呤浓度。我们的研究结果总结于表1。在我们的研究中,扁平苔藓患者的血清新蝶呤水平分为I组(9.12 +/- 4.39 ng/mL)和II组(3.80 +/- 0.68 ng/mL)以及整个收集的患者(I组和II组;6.55 +/- 2.30 ng/mL)显著高于对照组(2.55 +/- 0.34 ng/mL)。我们的研究结果证实了在扁平地衣中观察到的增强细胞免疫和巨噬细胞激活的作用。在我们看来,血清新蝶呤水平的评估,尽管特异性相对较低,但反映了广泛的病变和扁平苔藓的进展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Serum levels of neopterin in patients with lichen planus.

Lichen planus (LP) is a chronic dermatosis whose clinical features include mildly erythematous to violaceous flat-topped, polygonal papules. The etiology of lichen planus is unknown, but it has been postulated that immune mechanism is important. Although it is of importance to monitor the course of immune-mediated diseases, there is a limited number of reliable biomarkers which can be used for lichen planus. Neopterin (NP), a 2-amino-4-hydroxy-(1'2'3'-trihydroxypropyl)-pteridine, is secreted by monocytes and macrophages, mainly as a response to INF-gamma secretion by activated T-lymphocytes. Therefore NP may be a sensitive marker of T-cell mediated immunity. The aim of the presented study was to assess the serum levels of neopterin in patients with lichen planus and to investigate whether serum neopterin levels reflect extensive lesions and progression of this disease. We studied 66 patients with lichen planus who were classified into one of two diagnostic groups: Group I comprised 33 patients with generalized lesions; group II comprised 33 patients with circumscribed lesions. The control group consisted of 30 healthy sex- and age-matched individuals. The serum neopterin concentrations were measured with a commercially available enzyme-linked immunosorbent assay kit. The results of our study are summarized in Table 1. In our study, the serum neopterin levels in the patients with lichen planus classified to group I (9.12 +/- 4.39 ng/mL) and group II (3.80 +/- 0.68 ng/mL) as well as in the whole collection of patients (group I and group II; 6.55 +/- 2.30 ng/mL) were significantly higher than those of the control subjects (2.55 +/- 0.34 ng/mL). Our findings confirm a role for enhanced cellular immunity as well as macrophages activation observed in lichen planus. It seems to us that evaluation of serum neopterin levels, despite the relatively low specificity, reflects extensive lesions and lichen planus progression.

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