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[淋巴细胞活化标志物作为炎症中免疫系统失调的指标]

[Activation markers of lymphocytes as indicators of immune system dysregulation in inflammation].

作者信息

Poriadin G V, Salmasi Zh M, Kazimiskiĭ A N

出版信息

Patol Fiziol Eksp Ter. 2006 Jan-Mar(1):2-7.

Abstract

Three groups of activation antigens (receptors) of human peripheral blood lymphocytes (CD23, CD54--functional activation antigens, CD25 and CD71--early activation antigens and HLA-DR and CD95--late activation antigens) were studied in patients with inflammatory diseases of different types. All kinds of inflammation are independent of etiological factors and are associated with immune system activation. Inflammation induced by tissue injury or invasion of nonspecific microorganisms leads to a rapid rise in the count of lymphocytes expressing early markers of activation. Inhibition of inflammation occurs with a significant rise in peripheral blood lymphocytes with receptor of activation apoptosis CD95 (Fas-antigen). High number of lymphocytes with early markers of activation in line with high number of blood CD95+ lymphocytes take place in allergic and autoimmune diseases for a long time. Abnormal regulation of activation processes in lymphocytes in allergic and autoimmune diseases consists in the absence of lymphocyte activation inhibition in spite of high expression of CD95.

摘要

在患有不同类型炎症性疾病的患者中,研究了人类外周血淋巴细胞的三组激活抗原(受体)(CD23、CD54——功能性激活抗原,CD25和CD71——早期激活抗原,以及HLA-DR和CD95——晚期激活抗原)。各类炎症均独立于病因因素,且与免疫系统激活相关。由组织损伤或非特异性微生物入侵引发的炎症会导致表达激活早期标志物的淋巴细胞数量迅速增加。炎症的抑制伴随着外周血中带有激活凋亡受体CD95(Fas抗原)的淋巴细胞显著增多而发生。在过敏性和自身免疫性疾病中,长期存在大量带有激活早期标志物的淋巴细胞以及大量血液中CD95+淋巴细胞。在过敏性和自身免疫性疾病中,淋巴细胞激活过程的异常调节表现为尽管CD95表达较高,但仍缺乏淋巴细胞激活抑制。

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