New antibiotics for selective treatment of gastrointestinal infection caused by Clostridium difficile

被引:15
作者
Johnson, Alan P. [1 ]
机构
[1] Hlth Protect Agcy Ctr Infect, Dept Healthcare Associated Infect & Antimicrobial, London NW9 5EQ, England
关键词
antibiotic-associated diarrhoea; fidaxomicin; nitazoxanide; NVB302; oritavancin; REP3123; IN-VITRO ACTIVITY; INTESTINAL BACTERIA; NITAZOXANIDE; OPT-80; VANCOMYCIN; COLITIS; REP3123; SUSCEPTIBILITY; METRONIDAZOLE; ORITAVANCIN;
D O I
10.1517/13543776.2010.511177
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Importance of the field: Clostridium difficile infection (CDI) is associated with consumption of antibiotics which disrupt the normal microbial flora of the gut, allowing C. difficile to establish itself and produce disease. Currently, only vancomycin or metronidazole are recommended for treatment and many patients suffer from relapse on infection. Hence, there is a need for new treatment options. Areas covered in this review: This review evaluates five agents in development where the focus is on treatment of CDI. What the reader will gain: This review gives up-to-date information on fidaxomicin, REP3123, oritavancin, NVB302 and nitazoxanide and their likelihood of being licensed for the treatment of CDI. Take home message: One agent, fidaxomicin, has undergone Phase III clinical trials which show it to be a promising new agent for the treatment of CDI with a low rate of relapse. Nitazoxanide is licensed for the treatment of parasitic intestinal infections but is not licensed for CDI. However, in small scale clinical trials it has been shown to have activity comparable to that of vancomycin and metronidazole. The other agents are all at early stages of development and clinical trials to evaluate their therapeutic potential for CDI have not yet been undertaken.
引用
收藏
页码:1389 / 1399
页数:11
相关论文
共 58 条
[1]   In vitro activity of OPT-80 against clostridium difcile [J].
Ackermann, G ;
Löffler, B ;
Adler, D ;
Rodloff, AC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (06) :2280-2282
[2]  
BABAKHANI E, 2004, 44 INT C ANT AG CHEM
[3]  
BAINES SD, 2009, 49 INT C ANT AG CHEM
[4]   Emergence of reduced susceptibility to metronidazole in Clostridium difficile [J].
Baines, Simon D. ;
O'Connor, Rachael ;
Freeman, Jane ;
Fawley, Warren N. ;
Harmanus, Celine ;
Mastrantonio, Paola ;
Kuijper, Ed J. ;
Wilcox, Mark H. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2008, 62 (05) :1046-1052
[5]   Comparison of oritavancin versus vancomycin as treatments for clindamycin-induced Clostridium difficile PCR ribotype 027 infection in a human gut model [J].
Baines, Simon D. ;
O'Connor, Rachael ;
Saxton, Katie ;
Freeman, Jane ;
Wilcox, Mark H. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2008, 62 (05) :1078-1085
[6]   What have we learned about antimicrobial use and the risks for Clostridium difficile-associated diarrhoea? [J].
Blondeau, J. M. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2009, 63 (02) :238-242
[7]   Typing and susceptibility of bacterial isolates from the fidaxomicin (OPT-80) phase II study for C. difficile infection [J].
Citron, D. M. ;
Babakhani, F. ;
Goldstein, E. J. C. ;
Nagaro, K. ;
Sambol, S. ;
Sears, P. ;
Shue, Y. -K. ;
Gerding, D. N. .
ANAEROBE, 2009, 15 (06) :234-236
[8]   Comparative in vitro activity of REP3123 against Clostridium difficile and other anaerobic intestinal bacteria [J].
Citron, Diane M. ;
Warren, Yumi A. ;
Tyrrell, Kerin L. ;
Merriam, Vreni ;
Goldstein, Ellie J. C. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2009, 63 (05) :972-976
[9]   Activity of OPT-80, a novel macrocycle, compared with those of eight other agents against selected anaerobic species [J].
Credito, KL ;
Appelbaum, PC .
ANTIMICROBIAL AGENTS AND CHEMOTHERAPY, 2004, 48 (11) :4430-4434
[10]   Spectrum of activity and mode of action of REP3123, a new antibiotic to treat Clostridium difficile infections [J].
Critchley, Ian A. ;
Green, Louis S. ;
Young, Casey L. ;
Bullard, James M. ;
Evans, Ron J. ;
Price, Melissa ;
Jarvis, Thale C. ;
Guiles, Joseph W. ;
Janjic, Nebojsa ;
Ochsner, Urs A. .
JOURNAL OF ANTIMICROBIAL CHEMOTHERAPY, 2009, 63 (05) :954-963