Center for Anti-Infective Research and Development, Hartford Hospital, Hartford, Connecticut, USA.
Division of Infectious Diseases, Hartford Hospital, Hartford, Connecticut, USA.
Antimicrob Agents Chemother. 2023 May 17;67(5):e0173822. doi: 10.1128/aac.01738-22. Epub 2023 Apr 6.
The objective was to determine the magnitude of the EVER206 free-plasma area under the concentration time curve (AUC)/MIC target associated with bacteriostasis and 1-log kill against clinically relevant Gram-negative bacteria in the murine thigh model. Twenty-seven clinical isolates (Pseudomonas aeruginosa, = 10; Escherichia coli = 9; Klebsiella pneumoniae, = 5; Enterobacter cloacae, = 2; and Klebsiella aerogenes, = 1) were tested. Mice were pretreated with cyclophosphamide (induce neutropenia) and uranyl nitrate (increase the exposure of test compound through predictable renal dysfunction). Two hours postinoculation, five doses of EVER206 were administered subcutaneously. EVER206 pharmacokinetics were determined in infected mice. Data were fit using maximum effect () models to elucidate the AUC/MIC targets for stasis and 1-log bacterial kill (reported as mean [range] by species). EVER206 MICs (mg/L) ranged from 0.25 to 2 mg/L (P. aeruginosa), 0.06 to 2 mg/L (E. coli), 0.06 to 0.125 mg/L (E. cloacae), 0.06 mg/L (K. aerogenes), and 0.06 to 2 mg/L (K. pneumoniae). , the mean 0-h baseline bacterial burden was 5.57 ± 0.39 log CFU/thigh. Stasis was achieved in 9/10 P. aeruginosa (AUC/MIC, 88.13 [50.33 to 129.74]), 9/9 E. coli (AUC/MIC, 112.84 [19.19 to 279.38]), 2/2 E. cloacae (AUC/MIC, 259.28 [124.08 to 394.47]), 0/1 K. aerogenes, and 4/5 K. pneumoniae (AUC/MIC, 99.26 [62.3 to 144.43]) isolates tested. 1-log kill was achieved in 9/10 for P. aeruginosa (AUC/MIC, 106.43 [55.22 to 152.08]), 3/9 for E. coli (AUC/MIC, 258.96 [74.08 to 559.4]), and 1/2 for E. cloacae (AUC/MIC, 255.33). Using the murine thigh model, the AUC/MIC targets of EVER206 were assessed across a broad MIC distribution. Integrating these data with microbiologic and clinical exposure data will aid in determining the clinical dose of EVER206.
目的是确定 EVER206 游离血浆面积与浓度时间曲线下面积(AUC)/MIC 目标相关的程度,该目标与临床相关的革兰氏阴性菌在鼠大腿模型中的抑菌和 1 对数杀灭有关。测试了 27 株临床分离株(铜绿假单胞菌,10 株;大肠埃希菌,9 株;肺炎克雷伯菌,5 株;阴沟肠杆菌,2 株;和产气肠杆菌,1 株)。小鼠用环磷酰胺(诱导中性粒细胞减少症)和硝酸铀(通过可预测的肾功能障碍增加测试化合物的暴露)预处理。接种后 2 小时,皮下给予 EVER206 五次剂量。在感染的小鼠中确定 EVER206 的药代动力学。使用最大效应()模型拟合数据,以阐明停滞和 1 对数细菌杀灭的 AUC/MIC 目标(按种属报告为平均值[范围])。 EVER206 MIC(mg/L)范围为 0.25 至 2 mg/L(铜绿假单胞菌),0.06 至 2 mg/L(大肠埃希菌),0.06 至 0.125 mg/L(阴沟肠杆菌),0.06 mg/L(产气肠杆菌)和 0.06 至 2 mg/L(肺炎克雷伯菌)。在 0 小时时,平均基线细菌负荷为 5.57 ± 0.39 log CFU/大腿。在 10 株铜绿假单胞菌中的 9 株(AUC/MIC,88.13 [50.33 至 129.74])、9 株大肠埃希菌(AUC/MIC,112.84 [19.19 至 279.38])、2 株阴沟肠杆菌(AUC/MIC,259.28 [124.08 至 394.47])、0 株产气肠杆菌和 5 株肺炎克雷伯菌中的 4 株(AUC/MIC,99.26 [62.3 至 144.43])测试分离株达到了停滞状态。在 10 株铜绿假单胞菌中的 9 株(AUC/MIC,106.43 [55.22 至 152.08])、3 株大肠埃希菌(AUC/MIC,258.96 [74.08 至 559.4])和 2 株阴沟肠杆菌(AUC/MIC,255.33)中达到了 1 对数杀灭。使用鼠大腿模型,评估了 EVER206 在广泛 MIC 分布中的 AUC/MIC 目标。将这些数据与微生物学和临床暴露数据相结合,将有助于确定 EVER206 的临床剂量。