Chemotaxis inhibitory protein of Staphylococcus aureus, a bacterial antiinflammatory agent

被引:341
作者
de Haas, CJC
Veldkamp, KE
Peschel, A
Weerkamp, F
Van Wamel, WJB
Heezius, ECJM
Poppelier, MJJG
Van Kessel, KPM
van Strijp, JAG
机构
[1] Univ Utrecht, Med Ctr, Eijkman Winkler Inst, NL-3584 CX Utrecht, Netherlands
[2] Univ Tubingen, Cellular & Mol Microbiol Med Microbiol & Hyg Dept, D-72076 Tubingen, Germany
关键词
Staphylococcus aureus; phagocytes; chemotaxis; C5a; formylated peptides;
D O I
10.1084/jem.20031636
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Leukocyte migration is a key event both in host defense against invading pathogens as well as in inflammation. Bacteria generate chemoattractants primarily by excretion (formylated peptides), complement activation(C5a), and subsequently through activation of leukocytes (e.g., leukotriene B4, platelet-activating factor, and interleukin 8). Here we describe a new protein secreted by Staphylococcus aureus that specifically impairs the response of neutrophils and monocytes to formylated peptides and C5a. This chemotaxis inhibitory protein of S. aureus (CHIPS) is a 14.1-kD protein encoded on a bacteriophage and is found in >60% of clinical isolates. CHIPS reduces the neutrophil recruitment toward C5a in a mouse peritonitis model, even though its activity is much more potent on human than on mouse cells. These findings suggest a new immune escape mechanism of S. aureus and put forward CHIPS as a potential new antiinflammatory therapeutic compound.
引用
收藏
页码:687 / 695
页数:9
相关论文
共 44 条
  • [11] On the edge: the physiological and pathophysiological role of chemokines during inflammatory and immunological responses
    DeVries, ME
    Ran, L
    Kelvin, DJ
    [J]. SEMINARS IN IMMUNOLOGY, 1999, 11 (02) : 95 - 104
  • [12] Exotoxins of Staphylococcus aureus
    Dinges, MM
    Orwin, PM
    Schlievert, PM
    [J]. CLINICAL MICROBIOLOGY REVIEWS, 2000, 13 (01) : 16 - +
  • [13] DOHLSTEN M, 1993, IMMUNOLOGY, V79, P520
  • [14] Ferguson SSG, 2001, PHARMACOL REV, V53, P1
  • [15] THE CHEMOTACTIC RECEPTOR FOR HUMAN-C5A ANAPHYLATOXIN
    GERARD, NP
    GERARD, C
    [J]. NATURE, 1991, 349 (6310) : 614 - 617
  • [16] Coevolutionary patterns in plasminogen activation
    Gladysheva, IP
    Turner, RB
    Sazonova, IY
    Liu, L
    Reed, GL
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2003, 100 (16) : 9168 - 9172
  • [17] A STAPHYLOCOCCAL AGGRESSIN
    HILL, MJ
    [J]. JOURNAL OF MEDICAL MICROBIOLOGY, 1968, 1 (01) : 33 - &
  • [18] COMPLEMENT-INDUCED GRANULOCYTE AGGREGATION - IMPORTANCE IN MYOCARDIAL-INFARCTION AND SHOCK LUNG
    JACOB, HS
    HAMMERSCHMIDT, DE
    [J]. JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1981, 245 (20): : 2013 - &
  • [19] MEASUREMENT OF THE CHEMOTACTIC COMPLEMENT FRAGMENT C5A IN RHEUMATOID SYNOVIAL-FLUIDS BY RADIOIMMUNOASSAY - ROLE OF C5A IN THE ACUTE INFLAMMATORY PHASE
    JOSE, PJ
    MOSS, IK
    MAINI, RN
    WILLIAMS, TJ
    [J]. ANNALS OF THE RHEUMATIC DISEASES, 1990, 49 (10) : 747 - 752
  • [20] Calmodulin regulates L-selectin adhesion molecule expression and function through a protease-dependent mechanism
    Kahn, J
    Walcheck, B
    Migaki, GI
    Jutila, MA
    Kishimoto, TK
    [J]. CELL, 1998, 92 (06) : 809 - 818