Enterococcal infections: host response, therapeutic, and prophylactic possibilities

被引:108
作者
Koch, S
Hufnagel, M
Theilacker, C
Huebner, J
机构
[1] Brigham & Womens Hosp, Channing Lab, Dept Med, Boston, MA 02115 USA
[2] Univ Childrens Hosp Kiel, D-24105 Kiel, Germany
[3] Res Ctr Borstel, D-23845 Borstel, Germany
[4] Harvard Univ, Childrens Hosp, Sch Med, Div Infect Dis, Boston, MA 02115 USA
关键词
enterococcus; vaccine; therapeutic antibodies;
D O I
10.1016/j.vaccine.2003.11.027
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The emergence of resistance against multiple antibiotics and the increasing frequency with which Enterococcus faecalis and Enterococcus faecium are isolated from hospitalized patients underscore the necessity for a better understanding of the virulence mechanisms of this pathogen and the development of alternatives to current antibiotic treatments. The genetic plasticity of enterococci and their ability to rapidly acquire and/or develop resistance against many clinically important antibiotics and to transfer these resistance determinants to other more pathogenic microorganisms makes the search for alternative treatment and preventive options even more important. A capsular polysaccharide antigen has recently been characterized that is the target of,opsonic antibodies. A limited number of clinically relevant serotypes exist, and the development of an enterococcal vaccine based on capsular polysaccharides may improve our ability to prevent and treat these infections. Additional enterococcal surface antigens, including ABC transporter proteins and other virulence factors, such as aggregation substance (AS), may also be useful targets for therapeutic antibodies. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:822 / 830
页数:9
相关论文
共 129 条
[91]   Effects of Enterococcus faecalis fsr genes on production of gelatinase and a serine protease and virulence [J].
Qin, X ;
Singh, KV ;
Weinstock, GM ;
Murray, BE .
INFECTION AND IMMUNITY, 2000, 68 (05) :2579-2586
[92]   Characterization of fsr, a regulator controlling expression of gelatinase and serine protease in Enterococcus faecalis OG1RF [J].
Qin, X ;
Singh, KV ;
Weinstock, GM ;
Murray, BE .
JOURNAL OF BACTERIOLOGY, 2001, 183 (11) :3372-3382
[93]   Inventory, assembly and analysis of Bacillus subtilis ABC transport systems [J].
Quentin, Y ;
Fichant, G ;
Denizot, F .
JOURNAL OF MOLECULAR BIOLOGY, 1999, 287 (03) :467-484
[94]   Enterococcus faecalis bearing aggregation substance is resistant to killing by human neutrophils despite phagocytosis and neutrophil activation [J].
Rakita, RM ;
Vanek, NN ;
Jacques-Palaz, K ;
Mee, M ;
Mariscalco, MM ;
Dunny, GM ;
Snuggs, M ;
van Winkle, WB ;
Simon, SI .
INFECTION AND IMMUNITY, 1999, 67 (11) :6067-6075
[95]   Ace is a collagen-binding MSCRAMM from Enterococcus faecalis [J].
Rich, RL ;
Kreikemeyer, B ;
Owens, RT ;
LaBrenz, S ;
Narayana, SVL ;
Weinstock, GM ;
Murray, BE ;
Höök, M .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1999, 274 (38) :26939-26945
[96]   Nosocomial infections in combined medical-surgical intensive care units in the United States [J].
Richards, MJ ;
Edwards, JR ;
Culver, DH ;
Gaynes, RP .
INFECTION CONTROL AND HOSPITAL EPIDEMIOLOGY, 2000, 21 (08) :510-515
[97]   Nosocomial infections in medical intensive care units in the United States [J].
Richards, MJ ;
Edwards, JR ;
Culver, DH ;
Gaynes, RP .
CRITICAL CARE MEDICINE, 1999, 27 (05) :887-892
[98]   The commonality of risk factors for nosocomial colonization and infection with antimicrobial-resistant Staphylococcus aureus, enterococcus, gram-negative bacilli, Clostridium difficile, and Candida [J].
Safdar, N ;
Maki, DG .
ANNALS OF INTERNAL MEDICINE, 2002, 136 (11) :834-844
[99]   CHARACTERIZATION OF A CLASS OF NONFORMYLATED ENTEROCOCCUS-FAECALIS-DERIVED NEUTROPHIL CHEMOTACTIC PEPTIDES - THE SEX-PHEROMONES [J].
SANNOMIYA, P ;
CRAIG, RA ;
CLEWELL, DB ;
SUZUKI, A ;
FUJINO, M ;
TILL, GO ;
MARASCO, WA .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1990, 87 (01) :66-70
[100]   Aggregation substance increases adherence and internalization, but not translocation, of Enterococcus faecalis through different intestinal epithelial cells in vitro [J].
Sartingen, S ;
Rozdzinski, E ;
Muscholl-Silberhorn, A ;
Marre, R .
INFECTION AND IMMUNITY, 2000, 68 (10) :6044-6047