Cathelicidin peptides as candidates for a novel class of antimicrobials

被引:104
作者
Zanetti, M
Gennaro, R
Skerlavaj, B
Tomasinsig, L
Circo, R
机构
[1] Univ Udine, Dipartimento Sci & Tecnol Biomed, I-33100 Udine, Italy
[2] Lab Nazl CIB, Area Sci Pk, I-34012 Trieste, Italy
[3] Univ Trieste, Dipartimento Biochim Biofis & Chim Macromol, I-34127 Trieste, Italy
关键词
D O I
10.2174/1381612023395457
中图分类号
R9 [药学];
学科分类号
1007 ;
摘要
Cathelicidin peptides are a numerous group of mammalian cationic antimicrobial peptides. Despite a common evolutionary origin of their genes, peptides display a remarkable variety of sizes, sequences and structures. Their spectra of antimicrobial activity are varied and cover a range of organisms that includes bacteria, fungi and enveloped viruses. In addition, they bind to and neutralize the effects of endotoxin. These features make this family of peptides good candidates in view of a therapeutic use. The most promising ones are currently under evaluation as leads for the development of novel anti-infectives, and synthetic variants are in an advanced stage of development for specific clinical applications. This review focuses on recent studies on the structure and in vitro and in vivo biological activities of these peptides.
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收藏
页码:779 / 793
页数:15
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