In Vivo Pharmacodynamic Profile of EVER206, a Novel Polymyxin Antimicrobial, against Gram-Negative Bacteria in the Murine Thigh Infection Model

被引:0
作者
Gill, Christian M. [1 ]
Nicolau, David P. [1 ,2 ]
机构
[1] Hartford Hosp, Ctr Antiinfect Res & Dev, Hartford, CT 06106 USA
[2] Hartford Hosp, Div Infect Dis, Hartford, CT USA
关键词
EVER206; SPR206; Gram-negative bacteria; in vivo; pharmacodynamics; pharmacokinetics; LUNG INFECTION; STREPTOCOCCUS-PNEUMONIAE; PSEUDOMONAS-AERUGINOSA; MOUSE THIGH; COLISTIN; RESISTANT;
D O I
10.1128/aac.01738-22
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
The objective was to determine the magnitude of the EVER206 free-plasma area under the concentration time curve (fAUC)/MIC target associated with bacteriostasis and 1-log(10) kill against clinically relevant Gram-negative bacteria in the murine thigh model. Twenty-seven clinical isolates (Pseudomonas aeruginosa, n = 10; Escherichia coli, n = 9; Klebsiella pneumoniae, n = 5; Enterobacter cloacae, n = 2; and Klebsiella aerogenes, n = 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 (E-max) models to elucidate the fAUC/MIC targets for stasis and 1-log(10) 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). In vivo, the mean 0-h baseline bacterial burden was 5.57 +/- 0.39 log(10) CFU/thigh. Stasis was achieved in 9/10 P. aeruginosa (fAUC/MIC, 88.13 [50.33 to 129.74]), 9/9 E. coli (fAUC/MIC, 112.84 [19.19 to 279.38]), 2/2 E. cloacae (fAUC/MIC, 259.28 [124.08 to 394.47]), 0/1 K. aerogenes, and 4/5 K. pneumoniae (fAUC/MIC, 99.26 [62.3 to 144.43]) isolates tested. 1-log(10) kill was achieved in 9/10 for P. aeruginosa (fAUC/MIC, 106.43 [55.22 to 152.08]), 3/9 for E. coli (fAUC/MIC, 258.96 [74.08 to 559.4]), and 1/2 for E. cloacae (fAUC/MIC, 255.33). Using the murine thigh model, the fAUC/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. The objective was to determine the magnitude of the EVER206 free-plasma area under the concentration time curve (fAUC)/MIC target associated with bacteriostasis and 1-log(10) kill against clinically relevant Gram-negative bacteria in the murine thigh model. Twenty-seven clinical isolates (Pseudomonas aeruginosa, n = 10; Escherichia coli, n = 9; Klebsiella pneumoniae, n = 5; Enterobacter cloacae, n = 2; and Klebsiella aerogenes, n = 1) were tested.
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共 29 条
[1]  
Abdelraouf K, 2017, ANTIMICROB AGENTS CH, V61, DOI [10.1128/AAC.01957-16, 10.1128/aac.01957-16]
[2]   Pharmacokinetics-pharmacodynamics of antimicrobial therapy: It's not just for mice anymore [J].
Ambrose, Paul G. ;
Bhavnani, Sujata M. ;
Rubino, Christopher M. ;
Louie, Arnold ;
Gumbo, Tawanda ;
Forrest, Alan ;
Drusano, George L. .
CLINICAL INFECTIOUS DISEASES, 2007, 44 (01) :79-86
[3]   Design of Next Generation Polymyxins with Lower Toxicity: The Discovery of SPR206 [J].
Brown, Pamela ;
Abbott, Elizabeth ;
Abdulle, Omar ;
Boakes, Steven ;
Coleman, Scott ;
Divan, Naomi ;
Duperchy, Esther ;
Moss, Stephen ;
Rivers, Dean ;
Simonovic, Mona ;
Singh, Jaspal ;
Stanway, Steven ;
Wilson, Antoinette ;
Dawson, Michael J. .
ACS INFECTIOUS DISEASES, 2019, 5 (10) :1645-1656
[4]   Single- and Multiple-Ascending-Dose Study of the Safety, Tolerability, and Pharmacokinetics of the Polymyxin Derivative SPR206 [J].
Bruss, Jon ;
Lister, Troy ;
Gupta, Vipul K. ;
Stone, Emily ;
Morelli, Lisa ;
Lei, Yang ;
Melnick, David .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2021, 65 (10)
[5]  
Bulitta JB, 2019, ANTIMICROB AGENTS CH, V63, DOI [10.1128/aac.02307-18, 10.1128/AAC.02307-18]
[6]   New pharmacokinetic/pharmacodynamic studies of systemically administered colistin against Pseudomonas aeruginosa and Acinetobacter baumannii in mouse thigh and lung infection models: smaller response in lung infection [J].
Cheah, Soon-Ee ;
Wang, Jiping ;
Van Thi Thu Nguyen ;
Turnidge, John D. ;
Li, Jian ;
Nation, Roger L. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2015, 70 (12) :3291-3297
[7]  
CLSI (Clinical and Laboratory Standards Institute), 2021, CLSI Supplement, VM100
[8]   Elucidation of the Pharmacokinetic/Pharmacodynamic Determinant of Colistin Activity against Pseudomonas aeruginosa in Murine Thigh and Lung Infection Models [J].
Dudhani, Rajesh V. ;
Turnidge, John D. ;
Coulthard, Kingsley ;
Milne, Robert W. ;
Rayner, Craig R. ;
Li, Jian ;
Nation, Roger L. .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2010, 54 (03) :1117-1124
[9]   Minocycline pharmacodynamics against Stenotrophomonas maltophilia in the neutropenic murine infection model: implications for susceptibility breakpoints [J].
Fratoni, Andrew J. ;
Nicolau, David P. ;
Kuti, Joseph L. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2022, 77 (04) :1052-1060
[10]   In vivo translational assessment of the GES genotype on the killing profile of ceftazidime, ceftazidime/avibactam and meropenem against Pseudomonas aeruginosa [J].
Gill, Christian M. ;
Oliver, Antonio ;
Fraile-Ribot, Pablo Arturo ;
Nicolau, David P. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2022, 77 (10) :2803-2808