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静脉注射用单体IgG制剂可抑制聚合IgG对血小板的刺激。

Monomeric IgG preparations for intravenous use inhibit platelet stimulation by polymeric IgG.

作者信息

Gross B, Haessig A, Luescher E F, Nydegger U E

出版信息

Br J Haematol. 1983 Feb;53(2):289-99. doi: 10.1111/j.1365-2141.1983.tb02023.x.

Abstract

Seven different immunoglobulin G (IgG) preparations for intravenous use were tested for their capacity to inhibit serotonin-release from washed human platelets induced by IgG coupled with bis-diazobenzidine. Using a reference standard consisting of the top third fraction of an ultracentrifuged gammaglobulin preparation for intramuscular use, two chemically treated preparations were less potent inhibitors than the standard while two preparations, one pH 4 treated and another albumin protected, were better inhibitors. A pepsin treated preparation was devoid of inhibitory capacity, whereas Fc fragments derived from human IgG were extremely efficient. Evidence is discussed that the inhibitory capacity is inversely correlated to the content of oligo- and/or dimeric IgG molecules.

摘要

对七种不同的静脉注射用免疫球蛋白G(IgG)制剂进行了测试,以检测它们抑制由与双偶氮联苯胺偶联的IgG诱导的洗涤后人类血小板释放血清素的能力。使用由用于肌肉注射的超速离心丙种球蛋白制剂的上三分之一部分组成的参考标准品,两种化学处理的制剂作为抑制剂的效力低于标准品,而两种制剂,一种经pH 4处理,另一种有白蛋白保护,是更好的抑制剂。一种经胃蛋白酶处理的制剂没有抑制能力,而源自人类IgG的Fc片段则极其有效。讨论了抑制能力与寡聚和/或二聚IgG分子含量呈负相关的证据。

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