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静脉用多价免疫球蛋白在体外可干扰细胞增殖。

Polyvalent immunoglobulin for intravenous use interferes with cell proliferation in vitro.

作者信息

van Schaik I N, Lundkvist I, Vermeulen M, Brand A

机构信息

Department of Immunohematology and Bloodbank, University Hospital Leiden, The Netherlands.

出版信息

J Clin Immunol. 1992 Sep;12(5):325-34. doi: 10.1007/BF00920789.

Abstract

Intravenous immunoglobulin is used to an increasing extent in various immune-mediated diseases, but its mechanism(s) of action in vivo is incompletely understood. Previous studies have shown that intravenous immunoglobulin may interfere with autoantibodies and their production by B cells and also inhibit Fc-mediated antibody-dependent cytotoxicity. Here we describe a novel effect of intravenous immunoglobulin on proliferation of in vitro activated peripheral blood lymphocytes and autonomously growing cell lines of various origin. Independently of whether proliferation was autonomous or induced by antigen-specific or antigen-nonspecific reagents, proliferation was inhibited in a dose-dependent fashion, as measured by reduced 3H-thymidine and BrdU uptake and cell counting. The effect was not due to cytotoxic effects of intravenous immunoglobulin and was reversible after removing the intravenous immunoglobulin by washing. The IgG levels required for this inhibition of proliferation are supraphysiological but are reached in vivo during treatment with intravenous immunoglobulin.

摘要

静脉注射免疫球蛋白在各种免疫介导疾病中的应用日益广泛,但其体内作用机制尚未完全明确。先前的研究表明,静脉注射免疫球蛋白可能干扰自身抗体及其由B细胞产生的过程,还能抑制Fc介导的抗体依赖性细胞毒性。在此,我们描述了静脉注射免疫球蛋白对体外活化的外周血淋巴细胞以及各种来源的自主生长细胞系增殖的一种新作用。无论增殖是自主性的,还是由抗原特异性或抗原非特异性试剂诱导的,通过减少³H-胸腺嘧啶核苷和BrdU摄取以及细胞计数来衡量,增殖均呈剂量依赖性受到抑制。该作用并非由静脉注射免疫球蛋白的细胞毒性效应所致,通过洗涤去除静脉注射免疫球蛋白后,此作用是可逆的。抑制增殖所需的IgG水平高于生理水平,但在静脉注射免疫球蛋白治疗期间体内可达到该水平。

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