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大环内酯类药物对人吞噬功能的体外活性。

In vitro activity of macrolides on human phagocytic functions.

作者信息

Fietta A, Bersani C, Santagada T, Bertoletti R, Gialdroni Grassi G

出版信息

Chemioterapia. 1987 Feb;6(1):52-6.

PMID:3829136
Abstract

The aim of this study was to examine the in vitro activity of erythromycin, josamycin, flurithromycin, miocamycin and roxithromycin on some leukocyte functional parameters. All tested macrolides did not interfere with the frequency and index of phagocytosis, nitroblue tetrazolium reduction to formazan deposits and candidacidal activity of human polymorphonuclear leukocytes (p greater than 0.05). Among macrolide antibiotics, only flurithromycin significantly inhibited neutrophil chemotaxis at a high concentration (greater than or equal to 50 micrograms/ml). All macrolides, at 10 and 50 micrograms/ml, reduced the survival of a susceptible strain of Staphylococcus aureus ingested by human monocytes.

摘要

本研究的目的是检测红霉素、交沙霉素、氟红霉素、米欧卡霉素和罗红霉素对某些白细胞功能参数的体外活性。所有受试大环内酯类药物均未干扰人多形核白细胞的吞噬频率和指数、硝基蓝四氮唑还原为甲臜沉淀物以及杀念珠菌活性(P>0.05)。在大环内酯类抗生素中,只有氟红霉素在高浓度(≥50微克/毫升)时能显著抑制中性粒细胞趋化性。所有大环内酯类药物在10和50微克/毫升浓度时,均可降低被人单核细胞吞噬的金黄色葡萄球菌敏感菌株的存活率。

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