Center for Anti-Infective Research and Development, Hartford Hospital, 80 Seymour Street, Hartford, CT 06102, USA.
Research Planning Department, Shionogi & Co., Ltd, 3-1-1, Futaba-cho, Toyonaka,Osaka 561-0825, Japan.
J Antimicrob Chemother. 2023 Apr 3;78(4):983-990. doi: 10.1093/jac/dkad032.
Evaluate the in vivo efficacy and resistance prevention of cefiderocol in combination with ceftazidime/avibactam, ampicillin/sulbactam and meropenem using human-simulated regimens (HSR) in the murine infection model.
In total, 15 clinical A. baumannii were assessed: cefiderocol MICs, 2 mg/L (previously developed resistance on therapy), n = 3; 8 mg/L, n = 2; ≥32 mg/L, n = 10 (including VEB and PER-harbouring isolates). Mice received inactive control, cefiderocol, cefiderocol + ceftazidime/avibactam (C-CZA), cefiderocol + ampicillin/sulbactam (C-SAM) or cefiderocol + meropenem (C-MEM) HSRs. The mean change in log10 cfu/thigh compared with starting inoculum was assessed. Resistance development on treatment was a >4-fold increase in MIC relative control animals. In vitro activities of combinations were assessed by disc stacking.
Against cefiderocol-non-susceptible isolates, combinations produced significant kill with C-CZA -3.75 ± 0.37 reduction in log10 cfu/thigh, C-SAM produced -3.55 ± 0.50 and C-MEM produced -2.18 ± 1.75 relative to baseline. Elevated MICs in cefiderocol treated animals occurred in three out of three isolates with MICs of 2 mg/L. Of these isolates, one developed elevated MICs with C-MEM compared with none treated with C-CZA or C-SAM. Disc stacking with C-CZA or C-SAM returned all isolates to at least the CLSI intermediate breakpoint, which may correlate with in vivo efficacy.
Against cefiderocol-non-susceptible isolates, cefiderocol + ceftazidime/avibactam or ampicillin/sulbactam HSR produced in vivo kill against all 12 cefiderocol-non-susceptible isolates. Cefiderocol with ceftazidime/avibactam or ampicillin/sulbactam prevented the development of resistance during treatment against cefiderocol-high-end-susceptible isolates with a propensity for resistance on therapy. These data support the clinical evaluation of cefiderocol with ceftazidime/avibactam or ampicillin/sulbactam against A. baumannii, including multi-drug-resistant isolates.
使用人体模拟方案(HSR)在小鼠感染模型中评估头孢地尔在与头孢他啶/阿维巴坦、氨苄西林/舒巴坦和美罗培南联合使用时的体内疗效和耐药预防作用。
共评估了 15 株临床分离的鲍曼不动杆菌:头孢地尔 MICs,2 mg/L(之前治疗中产生耐药性),n = 3;8 mg/L,n = 2;≥32 mg/L,n = 10(包括 VEB 和 PER 携带株)。小鼠接受了无活性对照、头孢地尔、头孢地尔+头孢他啶/阿维巴坦(C-CZA)、头孢地尔+氨苄西林/舒巴坦(C-SAM)或头孢地尔+美罗培南(C-MEM)HSR。与起始接种物相比,评估了大腿中 log10 cfu 变化的平均值。与对照动物相比,MIC 增加 4 倍以上被认为是治疗中产生耐药性。通过圆盘堆积法评估组合的体外活性。
对于头孢地尔不敏感的分离株,C-CZA 产生了显著的杀菌作用,大腿中 log10 cfu 的减少量为 -3.75 ± 0.37,C-SAM 产生了 -3.55 ± 0.50,C-MEM 产生了 -2.18 ± 1.75。在接受头孢地尔治疗的动物中,有三株 2 mg/L MIC 的分离株 MIC 升高。在这些分离株中,与未用 C-CZA 或 C-SAM 治疗的分离株相比,一株分离株对 C-MEM 的 MIC 升高。与 C-CZA 或 C-SAM 相比,圆盘堆积法使所有分离株至少恢复到 CLSI 中间折点,这可能与体内疗效相关。
对于头孢地尔不敏感的分离株,头孢地尔+头孢他啶/阿维巴坦或氨苄西林/舒巴坦 HSR 在体内对所有 12 株头孢地尔不敏感的分离株产生了杀菌作用。头孢地尔与头孢他啶/阿维巴坦或氨苄西林/舒巴坦联合使用可预防头孢地尔高敏性分离株在治疗过程中产生耐药性,这些分离株有治疗耐药性的倾向。这些数据支持头孢地尔与头孢他啶/阿维巴坦或氨苄西林/舒巴坦联合用于治疗鲍曼不动杆菌,包括多药耐药株的临床评估。