Antimicrobial and host-defense peptides as new anti-infective therapeutic strategies

被引:3323
作者
Hancock, Robert E. W.
Sahl, Hans-Georg
机构
[1] Univ British Columbia, Ctr Microbial Dis & Immun Res, Vancouver, BC V6T 1Z4, Canada
[2] Inst Med Microbiol & Immunol, Dept Pharmaceut Microbiol, D-53115 Bonn, Germany
基金
美国国家卫生研究院; 加拿大健康研究院;
关键词
D O I
10.1038/nbt1267
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Short cationic amphiphilic peptides with antimicrobial and/or immunomodulatory activities are present in virtually every life form, as an important component of ( innate) immune defenses. These host-defense peptides provide a template for two separate classes of antimicrobial drugs. Direct-acting antimicrobial host-defense peptides can be rapid-acting and potent, and possess an unusually broad spectrum of activity; consequently, they have prospects as new antibiotics, although clinical trials to date have shown efficacy only as topical agents. But for these compounds to fulfill their therapeutic promise and overcome clinical setbacks, further work is needed to understand their mechanisms of action and reduce the potential for unwanted toxicity, to make them more resistant to protease degradation and improve serum half-life, as well as to devise means of manufacturing them on a large scale in a consistent and cost-effective manner. In contrast, the role of cationic host-defense peptides in modulating the innate immune response and boosting infection-resolving immunity while dampening potentially harmful pro-inflammatory ( septic) responses gives these peptides the potential to become an entirely new therapeutic approach against bacterial infections.
引用
收藏
页码:1551 / 1557
页数:7
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