Wang Guoxing, Stange Eduard F, Wehkamp Jan
Institute of Clinical Pharmacology, Dr Margarete Fischer-Bosch Institute and University of Tübingen, Auerbachstr. 112, 70376 Stuttgart, Germany.
Expert Rev Anti Infect Ther. 2007 Dec;5(6):1049-57. doi: 10.1586/14787210.5.6.1049.
Defensins are endogenous antibiotics with microbicidal activity against Gram-negative and -positive bacteria, fungi, enveloped viruses and protozoa. A disturbed antimicrobial defense, as provided by Paneth and other epithelial cell defensins, seems to be a critical factor in the pathogenesis of Crohn's disease, an inflammatory disease of the intestinal tract. Different direct and indirect mechanisms leading to a breakdown of antimicrobial barrier function include direct changes in defensin gene numbers (e.g., copy number polymorphism), genetic mutations in pattern-recognition receptors (e.g., nucleotide-binding oligomerization domain 2) and, as described recently, a differentiation problem of epithelial stem cells mediated by the wingless type (Wnt) pathway. Knowledge regarding the regulation and biology of defensins provides an attractive target to open up new therapeutic avenues.
防御素是一种内源性抗生素,对革兰氏阴性菌和阳性菌、真菌、包膜病毒及原生动物具有杀菌活性。潘氏细胞和其他上皮细胞防御素所提供的抗菌防御功能紊乱,似乎是克罗恩病(一种肠道炎症性疾病)发病机制中的关键因素。导致抗菌屏障功能破坏的不同直接和间接机制包括防御素基因数量的直接变化(如拷贝数多态性)、模式识别受体的基因突变(如核苷酸结合寡聚化结构域2),以及最近所描述的由无翅型(Wnt)信号通路介导的上皮干细胞分化问题。有关防御素调节和生物学特性的知识为开辟新的治疗途径提供了一个有吸引力的靶点。