Extracellular-matrix-binding proteins as targets for the prevention of Staphylococcus aureus infections

被引:69
作者
Flock, JI [1 ]
机构
[1] Huddinge Univ Hosp, Karolinska Inst, Dept Immunol Microbiol Pathol & Infect Dis, S-14186 Huddinge, Sweden
来源
MOLECULAR MEDICINE TODAY | 1999年 / 5卷 / 12期
关键词
D O I
10.1016/S1357-4310(99)01597-X
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Staphylococcal infections cause a number of serious diseases, ranging from acute septicaemia to chronic problems such as osteomyelitis and septic arthritis. Resistance to antibiotics is a growing problem and has re-ignited interest in vaccines and in passive immunization with antibodies. Natural infections and vaccines based on whole bacteria lead to poor antibody responses, but recent research using animal models of several staphylococcal diseases reveals that vaccines based on recombinant staphylococcal extracellular-matrix-binding proteins are much mom protective. Passive immunization with antibodies against one of these proteins (collagen-binding protein) also shows promise in a mouse model of sepsis.
引用
收藏
页码:532 / 537
页数:6
相关论文
共 40 条
[1]   Autoinducer of virulence as a target for vaccine and therapy against Staphylococcus aureus [J].
Balaban, N ;
Goldkorn, T ;
Nhan, RT ;
Dang, LB ;
Scott, S ;
Ridgley, RM ;
Rasooly, A ;
Wright, SC ;
Larrick, JW ;
Rasooly, R ;
Carlson, JR .
SCIENCE, 1998, 280 (5362) :438-440
[2]   Immunogenicity of peptides derived from a fibronectin-binding protein of S-aureus expressed on two different plant viruses [J].
Brennan, FR ;
Jones, TD ;
Longstaff, M ;
Chapman, S ;
Bellaby, T ;
Smith, H ;
Xu, F ;
Hamilton, WDO ;
Flock, JI .
VACCINE, 1999, 17 (15-16) :1846-1857
[3]   Chimeric plant virus particles administered nasally or orally induce systemic and mucosal immune responses in mice [J].
Brennan, FR ;
Bellaby, T ;
Helliwell, SM ;
Jones, TD ;
Kamstrup, S ;
Dalsgaard, K ;
Flock, JI ;
Hamilton, WDO .
JOURNAL OF VIROLOGY, 1999, 73 (02) :930-938
[4]  
Brokke P, 1991, J Biomater Appl, V5, P204, DOI 10.1177/088532829100500305
[5]   Antibody response to fibronectin-binding adhesin FnbpA in patients with Staphylococcus aureus infections [J].
Casolini, F ;
Visai, L ;
Joh, D ;
Conaldi, PG ;
Toniolo, A ;
Höök, M ;
Speziale, P .
INFECTION AND IMMUNITY, 1998, 66 (11) :5433-5442
[6]   IMMUNOLOGICAL RESPONSE TO A STAPHYLOCOCCUS-AUREUS FIBRONECTIN-BINDING PROTEIN [J].
CIBOROWSKI, P ;
FLOCK, JI ;
WADSTROM, T .
JOURNAL OF MEDICAL MICROBIOLOGY, 1992, 37 (06) :376-381
[7]   Novel animal model for studying the molecular mechanisms of bacterial adhesion to bone-implanted metallic devices: Role of fibronectin in Staphylococcus aureus adhesion [J].
Fischer, B ;
Vaudaux, P ;
Magnin, M ;
ElMestikawy, Y ;
Proctor, RA ;
Lew, DP ;
Vasey, H .
JOURNAL OF ORTHOPAEDIC RESEARCH, 1996, 14 (06) :914-920
[8]   Reconsideration of the role of fibronectin binding in endocarditis caused by Staphylococcus aureus [J].
Flock, JI ;
Hienz, SA ;
Heimdahl, A ;
Schennings, T .
INFECTION AND IMMUNITY, 1996, 64 (05) :1876-1878
[9]   Surface protein adhesins of Staphylococcus aureus [J].
Foster, TJ ;
Höök, M .
TRENDS IN MICROBIOLOGY, 1998, 6 (12) :484-488
[10]   INFLUENCE OF STAPHYLOCOCCUS-AUREUS ANTIBODY ON EXPERIMENTAL ENDOCARDITIS IN RABBITS [J].
GREENBERG, DP ;
WARD, JI ;
BAYER, AS .
INFECTION AND IMMUNITY, 1987, 55 (12) :3030-3034