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
[1]  
[Anonymous], 43 INT C ANT AG CHEM
[2]   Comparison of tetracycline and tigecycline binding to ribosomes mapped by dimethylsulphate and drug-directed Fe2+ cleavage of 16S rRNA [J].
Bauer, G ;
Berens, C ;
Projan, SJ ;
Hillen, W .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2004, 53 (04) :592-599
[3]   In vitro activities of tigecycline (GAR-936) against recently isolated clinical bacteria in Spain [J].
Betriu, C ;
Rodríguez-Avial, I ;
Sánchez, BA ;
Gómez, M ;
Alvarez, J ;
Picazo, JJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2002, 46 (03) :892-895
[4]   In vitro activities of tigecycline against erythromycin-resistant Streptococcus pyogenes and Streptococcus agalactiae:: Mechanisms of macrolide and tetracycline resistance [J].
Betriu, C ;
Culebras, E ;
Rodríguez-Avial, I ;
Gómez, M ;
Sánchez, BA ;
Picazo, JJ .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (01) :323-325
[5]   Comparative in vitro activities of tigecycline (GAR-936) and other antimicrobial agents against Stenotrophomonas maltophilia [J].
Betriu, C ;
Rodríguez-Avial, I ;
Sánchez, BA ;
Gómez, M ;
Picazo, JJ .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2002, 50 (05) :758-759
[6]   In vitro antimicrobial activity of GAR-936 tested against antibiotic-resistant gram-positive blood stream infection isolates and strains producing extended-spectrum β-lactamases [J].
Biedenbach, DJ ;
Beach, ML ;
Jones, RN .
DIAGNOSTIC MICROBIOLOGY AND INFECTIOUS DISEASE, 2001, 40 (04) :173-177
[7]   In vitro activities of the glycylcycline GAR-936 against gram-positive bacteria [J].
Boucher, HW ;
Wennersten, CB ;
Eliopoulos, GM .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2000, 44 (08) :2225-2229
[8]   Determining incidence of extended spectrum β-lactamase producing Enterobacteriaceae, vancomycin-resistant Enterococcus faecium and methicillin-resistant Staphylococcus aureus in 38 centres from 17 countries:: the PEARLS study 2001-2002 [J].
Bouchillon, SK ;
Johnson, BM ;
Hoban, DJ ;
Johnson, JL ;
Dowzicky, MJ ;
Wu, DH ;
Visalli, MA ;
Bradford, PA .
INTERNATIONAL JOURNAL OF ANTIMICROBIAL AGENTS, 2004, 24 (02) :119-124
[9]   Antibacterial susceptibility of a vancomycin-resistant Staphylococcus aureus strain isolated at the Hershey Medical Center [J].
Bozdogan, B ;
Esel, D ;
Whitener, C ;
Browne, FA ;
Appelbaum, PC .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2003, 52 (05) :864-868
[10]   In Vitro activities of tigecycline (GAR-936) and 12 other antimicrobial agents against 90 Eikenella corrodens clinical isolates [J].
Cercenado, E ;
Cercenado, S ;
Bouza, E .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2003, 47 (08) :2644-2645