Center for Anti-Infective Research and Development, Hartford Hospital, Hartford, Connecticut, USA.
Antimicrob Agents Chemother. 2013 Jul;57(7):3299-306. doi: 10.1128/AAC.01989-12. Epub 2013 May 6.
Secondary to the stability of aztreonam against metallo-β-lactamases, coupled with avibatam's neutralizing activity against often coproduced extended-spectrum β-lactamases (ESBLs) or AmpC enzymes, the combination of aztreonam and avibactam has been proposed as a principal candidate for the treatment of infections with metallo-β-lactamase-producing Gram-negative organisms. Using the neutropenic-mouse thigh infection model, we evaluated the efficacy of human simulated doses of aztreonam-avibactam and aztreonam against 14 Enterobacteriaceae and 13 Pseudomonas aeruginosa isolates, of which 25 produced metallo-β-lactamases. Additionally, six P. aeruginosa isolates were also evaluated in immunocompetent animals. A humanized aztreonam dose of 2 g every 6 h (1-h infusion) was evaluated alone and in combination with avibactam at 375 or 600 mg every 6 h (1-h infusion), targeting the percentage of the dosing interval in which free-drug concentrations remained above the MIC (fT>MIC). Efficacy was evaluated as the change in bacterial density after 24 h compared with the bacterial density at the initiation of dosing. Aztreonam monotherapy resulted in reductions of two of the Enterobacteriaceae bacterial isolates (aztreonam MIC, ≤ 32 μg/ml; fT>MIC, ≥ 38%) and minimal activity against the remaining isolates (aztreonam MIC, ≥ 128 μg/ml; fT>MIC, 0%). Alternatively, aztreonam-avibactam therapy resulted in the reduction of all 14 Enterobacteriaceae isolates (aztreonam-avibactam MICs, ≤16 μg/ml; fT>MIC, ≥ 65%) and no difference between the 375- and 600-mg doses of avibactam was noted. Similar pharmacodynamically predictable activity against P. aeruginosa was noted in studies with neutropenic and immunocompetent mice, with activity occurring when the MICs were ≤ 16 μg/ml and variable efficacy noted when the MICs were ≥ 32 μg/ml. Again, no difference in efficacy between the 375- and 600-mg doses of avibactam was observed. Aztreonam-avibactam represents an attractive treatment option for infections with metallo-β-lactamase-producing Gram-negative pathogens that coproduce ESBLs or AmpC.
由于阿扎那韦对金属β-内酰胺酶的稳定性,加上阿维巴坦对经常共同产生的扩展谱β-内酰胺酶(ESBLs)或AmpC 酶的中和活性,阿扎那韦和阿维巴坦的联合已被提议作为治疗产金属β-内酰胺酶的革兰氏阴性菌感染的主要候选药物。使用中性粒细胞减少症小鼠大腿感染模型,我们评估了人类模拟剂量的阿扎那韦-阿维巴坦和阿扎那韦对 14 种肠杆菌科和 13 种铜绿假单胞菌分离株的疗效,其中 25 种产生了金属β-内酰胺酶。此外,还在免疫功能正常的动物中评估了 6 种铜绿假单胞菌分离株。评估了每 6 小时 2 克的人源化阿扎那韦剂量(1 小时输注)单独使用和与每 6 小时 375 或 600 毫克的阿维巴坦联合使用的疗效,以达到药物浓度超过 MIC 的时间百分比(fT>MIC)。疗效评估为与起始给药时的细菌密度相比,24 小时后细菌密度的变化。阿扎那韦单药治疗导致两种肠杆菌科细菌分离株的减少(阿扎那韦 MIC,≤32μg/ml;fT>MIC,≥38%),而对其余分离株的活性最小(阿扎那韦 MIC,≥128μg/ml;fT>MIC,0%)。相反,阿扎那韦-阿维巴坦治疗导致 14 种肠杆菌科分离株的减少(阿扎那韦-阿维巴坦 MIC,≤16μg/ml;fT>MIC,≥65%),并且阿维巴坦 375 和 600mg 剂量之间没有差异。在中性粒细胞减少症和免疫功能正常的小鼠研究中也观察到对铜绿假单胞菌具有相似的预测药效学活性,当 MICs≤16μg/ml 时出现活性,当 MICs≥32μg/ml 时观察到可变疗效。同样,阿维巴坦 375 和 600mg 剂量之间的疗效没有差异。阿扎那韦-阿维巴坦代表了治疗产金属β-内酰胺酶的革兰氏阴性病原体感染的一种有吸引力的治疗选择,这些病原体共同产生 ESBLs 或 AmpC。