Lack of correlation between in vitro immunological alterations and the development of scleroderma-like skin lesions in toxic oil syndrome patients.

Dermatologica Pub Date : 1991-01-01 DOI:10.1159/000247651
C Gutiérrez, M J Aparicio, M J Sánchez, E Cabrero
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引用次数: 1

Abstract

We examined whether immunological disturbances could influence the development of scleroderma-like skin lesions in patients affected by the Spanish toxic oil syndrome (TOS). To this end, peripheral blood mononuclear cells (PBMC) were collected from 13 chronic patients and 8 control subjects. All patients had suffered a toxic-induced severe neuromyopathy, and 6, in addition, had developed sclerodermoid skin manifestations. The phenotypic profile and the concentrations of interleukin-2 (IL-2) and of molecules with B cell differentiation factor IgG activity (BCDF-IgG) in supernatants of phytohemagglutinin-stimulated lymphocytes were analyzed both in patients and in normal controls. Molecules with BCDF-IgG activity were found increased in supernatants of mitogen-stimulated lymphocytes from TOS patients. Concentrations of IgG secreted by staphylococcus aureus-SAC-B blasts in the presence of TOS PBMC supernatant was 88 +/- 32.62 ng/ml (mean +/- 1 SD) versus 53 +/- 5.34 ng/ml in the presence of control supernatant (p less than 0.01). Levels of BCDF-IgG activity in TOS PBMC supernatants positively correlated with IgG serum levels (r = 0.69, p less than 0.01). The phenotypic profile of lymphocyte populations and the production of IL-2 were not altered in TOS subjects. No statistically significant differences were observed in the lymphocyte distribution nor in the IL-2 and BCDF-IgG production when comparing patients with or without scleroderma-like skin lesions. The results indicate that there was a dysfunction of the immune response in TOS subjects, which, however, was not sufficient for the development of the sclerodermoid lesions.

体外免疫改变与中毒性油综合征患者硬皮病样皮肤病变发展之间缺乏相关性。
我们研究了免疫紊乱是否会影响西班牙毒性油综合征(TOS)患者的硬皮病样皮肤病变的发展。为此,我们采集了13例慢性患者和8例对照者的外周血单个核细胞(PBMC)。所有患者均有中毒引起的严重神经肌病,另有6例出现硬皮样皮肤表现。分析了患者和正常人植物血凝素刺激淋巴细胞上清液中白细胞介素-2 (IL-2)和具有B细胞分化因子IgG活性的分子(BCDF-IgG)的表型特征和浓度。在有丝分裂原刺激淋巴细胞上清液中发现BCDF-IgG活性增高。TOS PBMC上清存在时,金黄色葡萄球菌- sac - b原细胞分泌的IgG浓度为88 +/- 32.62 ng/ml(平均+/- 1 SD),对照组上清存在时,IgG浓度为53 +/- 5.34 ng/ml (p < 0.01)。TOS PBMC上清液BCDF-IgG活性水平与血清IgG水平呈正相关(r = 0.69, p < 0.01)。淋巴细胞群的表型特征和IL-2的产生在TOS受试者中没有改变。与有无硬皮病样皮损的患者相比,淋巴细胞分布、IL-2和BCDF-IgG的产生均无统计学差异。结果表明,TOS患者存在免疫应答功能障碍,但这不足以导致硬皮样病变的发生。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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