Jacqueline Cedric, Asseray Nathalie, Batard Eric, Le Mabecque Virginie, Kergueris Marie-France, Dube Laurent, Bugnon Denis, Potel Gilles, Caillon Jocelyne
Laboratoire d'Antibiologie (UPRES EA-1156), UER de Médecine, 1 rue Gaston Veil, 44035 Nantes Cedex 01, France.
Int J Antimicrob Agents. 2004 Oct;24(4):393-6. doi: 10.1016/j.ijantimicag.2004.03.013.
Indifference or even antagonism has mainly been reported with combinations including linezolid. The presence of in vitro antagonism is not always correlated with in vivo failure. The purpose of this study was to evaluate the in vivo activity of linezolid combined with gentamicin using a methicillin-resistant Staphylococcus aureus (MRSA) endocarditis experimental model. A human-like pharmacokinetic simulation was used for linezolid and gentamicin to improve the extrapolation of the results to human therapy. Contrary to the antagonism previously described in vitro, linezolid combined with gentamicin exhibited bactericidal activity on the two strains with a decrease of at least 4 log(10)cfu/g of vegetation compared with controls. These data suggest that linezolid plus gentamicin could be an appropriate combination for the treatment of severe MRSA infections.
主要报道显示,含利奈唑胺的联合用药存在无反应甚至拮抗作用。体外拮抗作用的存在并不总是与体内治疗失败相关。本研究的目的是使用耐甲氧西林金黄色葡萄球菌(MRSA)心内膜炎实验模型评估利奈唑胺联合庆大霉素的体内活性。对利奈唑胺和庆大霉素进行了类人药代动力学模拟,以提高将结果外推至人类治疗的准确性。与先前体外描述的拮抗作用相反,利奈唑胺联合庆大霉素对两种菌株均表现出杀菌活性,与对照组相比,赘生物中细菌浓度至少降低4 log(10)cfu/g。这些数据表明,利奈唑胺加庆大霉素可能是治疗严重MRSA感染的合适联合用药。