Tigecycline: A new glycylcycline for treatment of serious infections

被引:165
作者
Noskin, GA
机构
[1] NW Mem Hosp, Div Infect Dis, Chicago, IL 60611 USA
[2] Northwestern Univ, Feinberg Sch Med, Dept Med, Chicago, IL 60611 USA
关键词
D O I
10.1086/431672
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Tigecycline is a new semisynthetic glycylcycline for the treatment of serious infections. Of the glycylcyclines, tigecycline is the most studied and appears to hold promise as a new antimicrobial agent that can be administered as monotherapy to patients with many types of serious bacterial infections. For patients with serious infections, the initial choice for empirical therapy with broad-spectrum antibiotics is crucial, and, if the choice is inappropriate, it may have adverse consequences for the patient. Tigecycline has been designed to overcome many existing mechanisms of resistance among bacteria and confers broad antibiotic coverage against vancomycin-resistant enterococci, methicillin-resistant Staphylococcus aureus, and many species of multidrug-resistant gram-negative bacteria. Tigecycline has been efficacious and well tolerated in human clinical phase 2 studies, which warranted further evaluation of tigecycline in larger studies for treatment of many indications, including complicated skin and skin-structure infections, complicated intra-abdominal infections, and infections of the lower respiratory tract.
引用
收藏
页码:S303 / S314
页数:12
相关论文
共 62 条
[21]   Comparative in vitro activities of GAR-936 against aerobic and anaerobic animal and human bite wound pathogens [J].
Goldstein, EJC ;
Citron, DM ;
Merriam, CV ;
Warren, Y ;
Tyrrell, K .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (10) :2747-2751
[22]   Antibiotic resistance among clinical isolates of Acinetobacter in the UK, and in vitro evaluation of tigecycline (GAR-936) [J].
Henwood, CJ ;
Gatward, T ;
Warner, M ;
James, D ;
Stockdale, MW ;
Spence, RP ;
Towner, KJ ;
Livermore, DM ;
Woodford, N .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 49 (03) :479-487
[23]   Effects of efflux transporter genes on susceptibility of Escheichia coli to tigecycline (GAR-936) [J].
Hirata, T ;
Saito, A ;
Nishino, K ;
Tamura, N ;
Yamaguchi, A .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (06) :2179-2184
[24]   Antipneumococcal activities of GAR-936 (a new glycylcycline) compared to those of nine other agents against penicillin-susceptible and -resistant pneumococci [J].
Hoellman, DB ;
Pankuch, GA ;
Jacobs, MR ;
Appelbaum, PC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (04) :1085-1088
[25]   In vitro activities of tigecycline against the Bacteroides fragilis group [J].
Jacobus, NV ;
McDermott, LA ;
Ruthazer, R ;
Snydman, DR .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (03) :1034-1036
[26]   Antimicrobial susceptibility of Gram-positive bacteria: What's current, What's anticipated? [J].
Johnson, AP ;
Livermore, DM ;
Tillotson, GS .
JOURNAL OF HOSPITAL INFECTION, 2001, 49 :S3-S11
[27]  
JOHNSON B, 2003, 43 INT C ANT AG CHEM, P257
[28]  
JOHNSON B, 2003, 43 INT C ANT AG CHEM, P206
[29]  
JONES R, 2004, 14 EUR C CLIN MICR I, P247
[30]   Susceptibilities of Mycoplasma hominis, M-pneumoniae, and Ureaplasma urealyticum to GAR-936, dalfopristin, dirithromycin, evernimicin, gatifloxacin, linezolid, moxifloxacin, quinupristin-dalfopristin, and telithromycin compared to their susceptibilities to reference macrolides, tetracyclines, and quinolones [J].
Kenny, GE ;
Cartwright, FD .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2001, 45 (09) :2604-2608