The Therapeutic Pipeline for Pseudomonas aeruginosa Infections

被引:65
作者
Burrows, Lori L. [1 ,2 ]
机构
[1] McMaster Univ, Dept Biochem & Biomed Sci, 4H18 Hlth Sci Ctr,1280 Main St West, Hamilton, ON L8S 4K1, Canada
[2] McMaster Univ, Michael G DeGroote Inst Infect Dis Res, 4H18 Hlth Sci Ctr,1280 Main St West, Hamilton, ON L8S 4K1, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
CYSTIC-FIBROSIS; ANTIBACTERIAL RESISTANCE; ANTIBIOTIC-RESISTANCE; BACTERIA; ADAPTATIONS; MECHANISMS; INHIBITORS; VIRULENCE; LPTD; AGE;
D O I
10.1021/acsinfecdis.8b00112
中图分类号
R914 [药物化学];
学科分类号
100701 ;
摘要
Pseudomonas aeruginosa is a Gram-negative opportunistic pathogen, designated by the World Health Organization as a critical priority for development of new therapeutics due to high levels of intrinsic and acquired antibiotic resistance. Other challenges include its versatility (it can persist in the environment and most strains are capable of causing disease in compromised hosts), robust efflux mechanisms that limit drug penetration, and the propensity to form antimicrobial-tolerant biofilms. Novel therapeutics in development to prevent or treat P. aeruginosa infections include vaccines, biologics such as antimicrobial peptides and therapeutic antibodies, virulence inhibitors, antimicrobials with novel targets, antibody-drug conjugates, resistance inhibitor-antibiotic or antibiotic-potentiator combinations, and bacteriophages or phage-derived lysins.
引用
收藏
页码:1041 / 1047
页数:13
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