[特应性皮炎患者血清t淋巴细胞抗原标记物的测定]。

Fiziologicheskiĭ zhurnal Pub Date : 1993-01-01
I A Bezvershenko, M G Boĭko, L D Kaliuzhnaia
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引用次数: 0

摘要

采用单克隆抗体OKT3、OKT8和OKT10(含二级125J标记抗小鼠IgG抗体)检测系统检测特应性皮炎患者血清中优球蛋白的含量。结果表明,患者血清中存在从t细胞表面脱落的CD3、CD8和CD38 t细胞标记抗原。选择免疫调节剂vilosen治疗成功的特应性皮炎患者,对其治疗前后的血清进行分析。治疗导致CD8、CD3决定因子的增加和OKT10抗体(CD38)决定抗原的减少。推测CD3和CD8决定因子的增加是由绒毛胶刺激t淋巴细胞增殖和抑制细胞功能引起的。由于CD38标记物主要存在于未成熟和活化的t细胞表面,而不存在于循环血液中,因此可以推测血清中正球蛋白部分中CD38的减少反映了这些决定因素从胸腺和外周淋巴器官的t细胞中脱落。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[The determination of T-lymphocyte antigenic markers in the serum of patients with atopic dermatitis].

The euglobulin fraction of serum of the patients with atopic dermatitis was studied using monoclonal antibodies OKT3, OKT8 and OKT10 in assay system including secondary 125J labeled anti-mouse IgG antibodies. It was shown that CD3, CD8 and CD38 T-cell marker antigens shed from the T-cell surface could be found in euglobulin fraction of serum patients. The patients with atopic dermatitis successfully treated with immunomodulator vilosen were selected and their serums obtained before and after treatment were investigated. The treatment resulted in the increase of CD8, CD3 determinants and a decrease of antigens determined by OKT10 antibodies (CD38). It is supposed that an increase of CD3 and CD8 determinants is caused by stimulation of T-lymphocyte proliferation and suppressor cell function by vilosen. Since CD38 marker is predominantly on the surface of immature and activated T-cells, which do not occur in circulating blood, it can be supposed that decrease of CD38 in the euglobulin fraction of serum reflects a shedding of these determinants from T-cells of thymus and peripheral lymphoid organs.

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