β-defensin 1 contributes to pulmonary innate immunity in mice

被引:178
作者
Moser, C
Weiner, DJ
Lysenko, E
Bals, R
Weiser, JN
Wilson, JM
机构
[1] 204 Wistar Inst, Philadelphia, PA 19104 USA
[2] Univ Penn, Dept Microbiol, Philadelphia, PA 19104 USA
[3] Univ Penn, Dept Pediat, Philadelphia, PA 19104 USA
[4] Childrens Hosp Philadelphia, Div Pulm Med, Philadelphia, PA 19104 USA
[5] Univ Penn, Dept Med, Inst Human Gene Therapy, Philadelphia, PA 19104 USA
[6] Univ Penn, Dept Mol & Cellular Engn, Philadelphia, PA 19104 USA
关键词
D O I
10.1128/IAI.70.6.3068-3072.2002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Innate immunity serves as a first line defense in vertebrate organisms by providing an initial barrier to microorganisms and triggering antigen-specific responses. Antimicrobial peptides are thought to be effectors of innate immunity through their antibiotic activity and direct killing of microorganisms. Evidence to support this hypothesis in vertebrates is indirect, based on expression profiles and in vitro assays using purified peptides. Here we investigated the function of antimicrobial peptides in vivo using mice deficient in an antimicrobial peptide, mouse beta-defensin-1 (mBD-1). We find that loss of mBD-1 results in delayed clearance of Haemophilus influenzae from lung. These data demonstrate directly that antimicrobial peptides of vertebrates provide an initial block to bacteria at epithelial surfaces.
引用
收藏
页码:3068 / 3072
页数:5
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