Phagocytosis and persistence of Helicobacter pylori

被引:78
作者
Allen, Lee-Ann H. [1 ]
机构
[1] Univ Iowa, Inflammat Program, Iowa City, IA 52242 USA
[2] Univ Iowa, Dept Med, Iowa City, IA 52242 USA
[3] Univ Iowa, Dept Microbiol, Iowa City, IA 52242 USA
[4] VA Med Ctr, Iowa City, IA 52242 USA
关键词
D O I
10.1111/j.1462-5822.2007.00906.x
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Helicobacter pylori is a spiral-shaped, flagellated, microaerophilic Gram-negative bacterium that colonizes the gastric epithelium of humans. All persons infected with H. pylori have gastritis, and some will develop severe disease such as peptic ulcers or gastric cancer. A characteristic feature of this infection is the pronounced accumulation of phagocytes, particularly neutrophils, in the gastric mucosa. H. pylori thrives in a phagocyte-rich environment, and we describe here how this organism uses an array of novel virulence factors to manipulate chemotaxis, phagocytosis, membrane trafficking and the respiratory burst as a means to evade elimination by the innate immune response.
引用
收藏
页码:817 / 828
页数:12
相关论文
共 112 条
[21]   THE ROLE OF HEPARAN SULFATE-BINDING ACTIVITY OF HELICOBACTER-PYLORI BACTERIA IN THEIR ADHESION TO MURINE MACROPHAGES [J].
CHMIELA, M ;
PAZIAKDOMANSKA, B ;
RUDNICKA, W ;
WADSTROM, T .
APMIS, 1995, 103 (06) :469-474
[22]   ATTACHMENT, INGESTION AND INTRACELLULAR KILLING OF HELICOBACTER-PYLORI BY HUMAN PERIPHERAL-BLOOD MONONUCLEAR LEUKOCYTES AND MOUSE PERITONEAL INFLAMMATORY MACROPHAGES [J].
CHMIELA, M ;
PAZIAKDOMANSKA, B ;
WADSTROM, T .
FEMS IMMUNOLOGY AND MEDICAL MICROBIOLOGY, 1995, 10 (3-4) :307-316
[23]  
Cornacchione P, 1998, IMMUNOLOGY, V93, P86
[24]   Helicobacter pylori virulence and genetic geography [J].
Covacci, A ;
Telford, JL ;
Del Giudice, G ;
Parsonnet, J ;
Rappuoli, R .
SCIENCE, 1999, 284 (5418) :1328-1333
[25]   Helicobacter pylori VacA, a paradigm for toxin multifunctionality [J].
Cover, TL ;
Blanke, SR .
NATURE REVIEWS MICROBIOLOGY, 2005, 3 (04) :320-332
[26]   A requirement for phosphatidylinositol 3-kinase in pseudopod extension [J].
Cox, D ;
Tseng, CC ;
Bjekic, G ;
Greenberg, S .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (03) :1240-1247
[27]   Respiratory burst in human neutrophils [J].
Dahlgren, C ;
Karlsson, A .
JOURNAL OF IMMUNOLOGICAL METHODS, 1999, 232 (1-2) :3-14
[28]   Co-expression in Helicobacter pylori of cagA and non-opsonic neutrophil activation enhances the association with peptic ulcer disease [J].
Danielsson, D ;
Farmery, SM ;
Blomberg, B ;
Perry, S ;
Rautelin, H ;
Crabtree, JE .
JOURNAL OF CLINICAL PATHOLOGY, 2000, 53 (04) :318-321
[29]  
Darwin P E, 1996, Helicobacter, V1, P20, DOI 10.1111/j.1523-5378.1996.tb00004.x
[30]   MUCOSAL REACTIVE OXYGEN METABOLITE PRODUCTION IN DUODENAL-ULCER DISEASE [J].
DAVIES, GR ;
SIMMONDS, NJ ;
STEVENS, TRJ ;
GRANDISON, A ;
BLAKE, DR ;
RAMPTON, DS .
GUT, 1992, 33 (11) :1467-1472