Staphylococcal innate immune evasion

被引:204
作者
Rooijakkers, SHM [1 ]
van Kessel, KPM [1 ]
van Strijp, JAG [1 ]
机构
[1] Univ Utrecht, Med Ctr, Eijkman Winkler Inst, NL-3584 CX Utrecht, Netherlands
关键词
D O I
10.1016/j.tim.2005.10.002
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
Upon entering the human body, bacteria are confronted with the sophisticated innate defense mechanisms of the human host. From work in recent years it has become obvious that a new and growing family of small and excreted proteins can counteract the antibacterial effects of innate immunity. These highly selective proteins pick out crucial elements of our immune system and inhibit their function. In Staphylococcus aureus these proteins act on specific cellular receptors, on antimicrobial peptides and especially on the complement system. The combined action of this growing group of essential virulence factors ascertains efficient innate immune evasion.
引用
收藏
页码:596 / 601
页数:6
相关论文
共 43 条
[21]   Innate defenses of the intestinal epithelial barrier [J].
Müller, CA ;
Autenrieth, IB ;
Peschel, A .
CELLULAR AND MOLECULAR LIFE SCIENCES, 2005, 62 (12) :1297-1307
[22]   Enhancement of complement activation and opsonophagocytosis by complexes of mannose-binding lectin with mannose-binding lectin-associated serine protease after binding to Staphylococcus aureus [J].
Neth, O ;
Jack, DL ;
Johnson, M ;
Klein, NJ ;
Turner, MW .
JOURNAL OF IMMUNOLOGY, 2002, 169 (08) :4430-4436
[23]   How do bacteria resist human antimicrobial peptides? [J].
Peschel, A .
TRENDS IN MICROBIOLOGY, 2002, 10 (04) :179-186
[24]   Residues 10-18 within the C5a receptor N terminus compose a binding domain for chemotaxis inhibitory protein of Staphylococcus aureus [J].
Postma, B ;
Kleibeuker, W ;
Poppelier, MJJG ;
Boonstra, M ;
Van Kessel, KPM ;
Van Strijp, JAG ;
de Haas, CJC .
JOURNAL OF BIOLOGICAL CHEMISTRY, 2005, 280 (03) :2020-2027
[25]   Chemotaxis inhibitory protein of Staphylococcus aureus binds specifically to the c5a and formylated peptide receptor [J].
Postma, B ;
Poppelier, MJ ;
van Galen, JC ;
Prossnitz, ER ;
van Strijp, JAG ;
de Haas, CJC ;
van Kessel, KPM .
JOURNAL OF IMMUNOLOGY, 2004, 172 (11) :6994-7001
[26]  
Projan S.J., 1997, The Staphylococci in human diseases, P55
[27]  
Rahimpour R, 1999, J IMMUNOL, V162, P2299
[28]   The contrasting mechanisms of serum resistance of Neisseria gonorrhoeae and group B Neisseria meningitidis [J].
Ram, S ;
Mackinnon, FG ;
Gulati, S ;
McQuillen, DP ;
Vogel, U ;
Frosch, M ;
Elkins, C ;
Guttormsen, HK ;
Wetzler, LM ;
Oppermann, M ;
Pangburn, MK ;
Rice, PA .
MOLECULAR IMMUNOLOGY, 1999, 36 (13-14) :915-928
[29]   Immune evasion by a staphylococcal complement inhibitor that acts on C3 convertases [J].
Rooijakkers, SHM ;
Ruyken, M ;
Roos, A ;
Daha, MR ;
Presanis, JS ;
Sim, RB ;
van Wamel, WJB ;
van Kessel, KPM ;
van Strijp, JAG .
NATURE IMMUNOLOGY, 2005, 6 (09) :920-927
[30]   Anti-opsonic properties of staphylokinase [J].
Rooijakkers, SHM ;
van Wamel, WJB ;
Ruyken, M ;
van Kessel, KPM ;
van Strijp, JAG .
MICROBES AND INFECTION, 2005, 7 (03) :476-484