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慢性淋巴细胞白血病中经典补体途径活性降低。

Depressed classical complement pathway activities in chronic lymphocytic leukaemia.

作者信息

Füst G, Czink E, Minh D, Miszlay Z, Varga L, Hollán S R

出版信息

Clin Exp Immunol. 1985 Jun;60(3):489-95.

Abstract

Haemolytic activities of the classical and alternative complement pathways, and levels of C1, C4, C3, factor B and C1 inhibitor (C1-INH) were measured in 85 serum samples from 46 patients with chronic lymphocytic leukaemia (CLL). Significantly decreased mean C1 and C4 levels were found, and the haemolytic activities of these components were low or low normal in more than 50% of the sera tested. In 15 sera from 5 patients a complement profile characteristic of acquired C1-IHN deficiency was observed. These results indicate that the depression of the activity of the classical complement pathway is a frequently occurring feature in CLL.

摘要

检测了46例慢性淋巴细胞白血病(CLL)患者85份血清样本中经典补体途径和替代补体途径的溶血活性,以及C1、C4、C3、B因子和C1抑制剂(C1-INH)的水平。发现平均C1和C4水平显著降低,且在超过50%的检测血清中,这些成分的溶血活性较低或处于低正常水平。在5例患者的15份血清中,观察到获得性C1-INH缺乏的补体特征。这些结果表明,经典补体途径活性降低是CLL中经常出现的特征。

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