In vivo study on the immunomodulating effects of OM-85 BV on survival, inflammatory cell recruitment and bacterial clearance in Klebsiella pneumonia

被引:8
作者
Broug-Holub, E [1 ]
Kraal, G [1 ]
机构
[1] Free Univ Amsterdam, Fac Med, Dept Cell Biol & Immunol, NL-1081 BT Amsterdam, Netherlands
来源
INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY | 1997年 / 19卷 / 9-10期
关键词
D O I
10.1016/S0192-0561(97)00083-0
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Oral administration of the bacterial extract OM-85 BV has been shown to prime alveolar macrophages (AM) in such a way that they secrete significantly more nitric oxide, tumor necrosis factor-alpha and interleukin-1 beta upon in vitro stimulation with lipopolysaccharide (LPS). As increased cytokine secretion by AM may account for the therapeutic effect of OM-85 BV in respiratory tract infections, we studied the effect of orally administered OM-85 BV on the outcome of Klebsiella pneumoniae-induced pneumonia. Mice received a daily oral dose of OM-85 BV (350 mg/kg body weight) for 5 days and were intratracheally infected with 333, 1000 or 3333 CFU K. pneumoniae on day 8. It was shown that OM-85 BV pretreatment of mice has no effect on bacterial clearance, neutrophil recruitment and survival in this acute respiratory tract infection. Also, OM-85 BV treatment had no protective effect in a recurrent infection with K. pneumoniae. It is concluded that AM activation by oral treatment with OM-85 BV is not sufficient to play a protective role in respiratory tract infection with K. pneumoniae. (C) 1998 Published by Elsevier Science Ltd on behalf of the International Society for Immunopharmacology.
引用
收藏
页码:559 / 564
页数:6
相关论文
共 21 条
  • [1] Alveolar macrophages are required for protective pulmonary defenses in murine Klebsiella pneumonia: Elimination of alveolar macrophages increases neutrophil recruitment but decreases bacterial clearance and survival
    BrougHolub, E
    Toews, GB
    VanIwaarden, JF
    Strieter, RM
    Kunkel, L
    Paine, R
    Standiford, TJ
    [J]. INFECTION AND IMMUNITY, 1997, 65 (04) : 1139 - 1146
  • [2] BROUGHOLUB E, 1995, CLIN EXP IMMUNOL, V101, P302
  • [3] MUCOSAL AND SYSTEMIC IMMUNIZATIONS WITH KILLED PSEUDOMONAS-AERUGINOSA PROTECT AGAINST ACUTE RESPIRATORY-INFECTION IN RATS
    CRIPPS, AW
    DUNKLEY, ML
    CLANCY, RL
    [J]. INFECTION AND IMMUNITY, 1994, 62 (04) : 1427 - 1436
  • [4] UP-REGULATION OF ADHESION MOLECULES INDUCED BY BRONCHO-VAXOM ON PHAGOCYTIC-CELLS
    DUCHOW, J
    MARCHANT, A
    DELVILLE, JP
    SCHANDENE, L
    GOLDMAN, M
    [J]. INTERNATIONAL JOURNAL OF IMMUNOPHARMACOLOGY, 1992, 14 (05): : 761 - 766
  • [5] EMMERICH B, 1987, ALLERGOLOGIE, V10, P447
  • [6] EFFECT OF ORAL IMMUNIZATION WITH PSEUDOMONAS-AERUGINOSA ON THE DEVELOPMENT OF SPECIFIC ANTIBACTERIAL IMMUNITY IN THE LUNGS
    FREIHORST, J
    MERRICK, JM
    OGRA, PL
    [J]. INFECTION AND IMMUNITY, 1989, 57 (01) : 235 - 238
  • [7] CYTOKINE-INDUCED SYNTHESIS OF NITROGEN-OXIDES IN MACROPHAGES - A PROTECTIVE HOST RESPONSE TO LEISHMANIA AND OTHER INTRACELLULAR PATHOGENS
    GREEN, SJ
    NACY, CA
    MELTZER, MS
    [J]. JOURNAL OF LEUKOCYTE BIOLOGY, 1991, 50 (01) : 93 - 103
  • [8] GREEN SJ, 1990, J IMMUNOL, V144, P278
  • [9] LOCAL AIRWAYS IMMUNE MODIFICATIONS INDUCED BY ORAL BACTERIAL EXTRACTS IN CHRONIC-BRONCHITIS
    LUSUARDI, M
    CAPELLI, A
    CARLI, S
    SPADA, EL
    SPINAZZI, A
    DONNER, CF
    [J]. CHEST, 1993, 103 (06) : 1783 - 1791
  • [10] MARCHANT A, 1992, RESPIRATION, V59, P24