Molecular basis of host-pathogen interaction in septic shock

被引:93
作者
Heumann, D [1 ]
Glauser, MP [1 ]
Calandra, T [1 ]
机构
[1] CHU Vaudois, Dept Internal Med, Div Infect Dis, CH-1011 Lausanne, Switzerland
关键词
D O I
10.1016/S1369-5274(98)80142-2
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Specific mechanisms of recognition of microbial products have been developed by host cells. Among these mechanisms, recognition of lipopolysaccharide of Gram-negative bacteria by CD14, a glycoprotein expressed at the surface of myelomonocytic cells, plays a major role. There is increasing evidence that CD14 also serves as a receptor for other microbial products including peptidoglycan of Gram-positive bacteria. A common theme is that CD14 represents a key molecule in innate immunity. Recognition of microbial products by host cells leads to cell activation and production of a large array of mediators that are necessary for the development of controlled inflammatory processes. When the activation process is out of control, such as in septic shock, these mediators can be detrimental to the host.
引用
收藏
页码:49 / 55
页数:7
相关论文
共 77 条
[71]   CR3 (CD11B/CD18) EXPRESSES ONE BINDING-SITE FOR ARG-GLY-ASP-CONTAINING PEPTIDES AND A 2ND SITE FOR BACTERIAL LIPOPOLYSACCHARIDE [J].
WRIGHT, SD ;
LEVIN, SM ;
JONG, MTC ;
CHAD, Z ;
KABBASH, LG .
JOURNAL OF EXPERIMENTAL MEDICINE, 1989, 169 (01) :175-183
[72]   CD14, A RECEPTOR FOR COMPLEXES OF LIPOPOLYSACCHARIDE (LPS) AND LPS BINDING-PROTEIN [J].
WRIGHT, SD ;
RAMOS, RA ;
TOBIAS, PS ;
ULEVITCH, RJ ;
MATHISON, JC .
SCIENCE, 1990, 249 (4975) :1431-1433
[73]   SOLUBLE CD14 ACTS AS A SHUTTLE IN THE NEUTRALIZATION OF LIPOPOLYSACCHARIDE (LPS) BY LPS-BINDING PROTEIN AND RECONSTITUTED HIGH-DENSITY-LIPOPROTEIN [J].
WURFEL, MM ;
HAILMAN, E ;
WRIGHT, SD .
JOURNAL OF EXPERIMENTAL MEDICINE, 1995, 181 (05) :1743-1754
[74]  
Wurfel MM, 1997, J IMMUNOL, V158, P3925
[75]   Lipopolysaccharide binding protein and soluble CD14 catalyze exchange of phospholipids [J].
Yu, B ;
Hailman, E ;
Wright, SD .
JOURNAL OF CLINICAL INVESTIGATION, 1997, 99 (02) :315-324
[76]  
Yu B, 1996, J BIOL CHEM, V271, P4100
[77]   MECHANISMS OF STIMULATION OF INTERLEUKIN-1-BETA AND TUMOR-NECROSIS-FACTOR-ALPHA BY MYCOBACTERIUM-TUBERCULOSIS COMPONENTS [J].
ZHANG, YH ;
DOERFLER, M ;
LEE, TC ;
GUILLEMIN, B ;
ROM, WN .
JOURNAL OF CLINICAL INVESTIGATION, 1993, 91 (05) :2076-2083