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孕妇疟疾间歇性预防治疗的抗菌活性:磺胺多辛-乙胺嘧啶、甲氟喹和阿奇霉素的体外比较研究。

Anti-bacterial activity of intermittent preventive treatment of malaria in pregnancy: comparative in vitro study of sulphadoxine-pyrimethamine, mefloquine, and azithromycin.

机构信息

Institute for Tropical Medicine, University of Tübingen, Tübingen, Germany.

出版信息

Malar J. 2010 Oct 29;9:303. doi: 10.1186/1475-2875-9-303.

Abstract

BACKGROUND

Intermittent preventive treatment of malaria with sulphadoxine-pyrimethamine (SP) is recommended for the prevention of malaria in pregnancy in sub-Saharan Africa. Increasing drug resistance necessitates the urgent evaluation of alternative drugs. Currently, the most promising candidates in clinical development are mefloquine and azithromycin. Besides the anti-malarial activity, SP is also a potent antibiotic and incurs significant anti-microbial activity when given as IPTp - though systematic clinical evaluation of this action is still lacking.

METHODS

In this study, the intrinsic anti-bacterial activity of mefloquine and azithromycin was assessed in comparison to sulphadoxine-pyrimethamine against bacterial pathogens with clinical importance in pregnancy in a standard microdilution assay.

RESULTS

SP was highly active against Staphylococcus aureus and Streptococcus pneumoniae. All tested Gram-positive bacteria, except Enterococcus faecalis, were sensitive to azithromycin. Additionally, azithromycin was active against Neisseria gonorrhoeae. Mefloquine showed good activity against pneumococci but lower in vitro action against all other tested pathogens.

CONCLUSION

These data indicate important differences in the spectrum of anti-bacterial activity for the evaluated anti-malarial drugs. Given the large scale use of IPTp in Africa, the need for prospective clinical trials evaluating the impact of antibiotic activity of anti-malarials on maternal and foetal health and on the risk of promoting specific drug resistance of bacterial pathogens is discussed.

摘要

背景

在撒哈拉以南非洲,推荐采用磺胺多辛-乙胺嘧啶(SP)间歇性预防治疗疟疾,以预防妊娠疟疾。随着耐药性的增加,迫切需要对替代药物进行评估。目前,临床开发中最有前途的候选药物是甲氟喹和阿奇霉素。除了抗疟活性外,SP 还是一种有效的抗生素,当作为 IPTp 给药时会产生显著的抗微生物活性 - 尽管对这种作用的系统临床评估仍然缺乏。

方法

在这项研究中,采用标准微量稀释法,比较了甲氟喹和阿奇霉素与磺胺多辛-乙胺嘧啶对妊娠期间具有临床重要性的细菌病原体的固有抗菌活性。

结果

SP 对金黄色葡萄球菌和肺炎链球菌高度有效。除粪肠球菌外,所有测试的革兰氏阳性菌均对阿奇霉素敏感。此外,阿奇霉素对淋病奈瑟菌也具有活性。甲氟喹对肺炎球菌表现出良好的活性,但对其他所有测试病原体的体外活性较低。

结论

这些数据表明,评估的抗疟药物的抗菌活性谱存在重要差异。鉴于 IPTp 在非洲的大规模使用,需要前瞻性临床试验来评估抗疟药物的抗生素活性对母婴健康和促进特定细菌病原体耐药性的风险的影响。

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