RECOMBINANT INTERLEUKIN-6 PROTECTS MICE AGAINST EXPERIMENTAL BACTERIAL-INFECTION

被引:57
作者
LIU, ZQ
SIMPSON, RJ
CHEERS, C
机构
[1] UNIV MELBOURNE, DEPT MICROBIOL, PARKVILLE, VIC 3052, AUSTRALIA
[2] ROYAL MELBOURNE HOSP, LUDWIG INST CANC RES, PARKVILLE, VIC 3050, AUSTRALIA
关键词
D O I
10.1128/IAI.60.10.4402-4406.1992
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Because of reports of high levels of interleukin-6 (IL-6) in patients during infection, we studied the role of IL-6 in experimental infection. Mice infected with the facultative intracellular pathogen Listeria monocytogenes displayed high levels of IL-6 in their sera and tissues, particularly the spleen, 1 to 3 days after infection. At this time, the IL-6 titers correlated with bacterial numbers in individual mice and in groups of mice given graded doses of Listeria organisms. However, the presence of IL-6 in serum declined after 4 days, even when a large initial dose of bacteria meant that bacterial numbers were still increasing at this time. Recombinant mouse IL-6 injected intraperitoneally before infection protected mice in a dose-dependent manner. It was effective when given 4 h before infection but not when administration was delayed for 24 h postinfection. It is therefore believed that IL-6 plays a role in early priming of the immune response to infection. Its exact function in this model is being investigated.
引用
收藏
页码:4402 / 4406
页数:5
相关论文
共 32 条
[1]  
CHANG HR, 1990, IMMUNOLOGY, V69, P33
[2]   MACROPHAGE PRODUCTION DURING MURINE LISTERIOSIS - COLONY-STIMULATING FACTOR-I (CSF-1) AND CSF-1-BINDING CELLS IN GENETICALLY RESISTANT AND SUSCEPTIBLE MICE [J].
CHEERS, C ;
STANLEY, ER .
INFECTION AND IMMUNITY, 1988, 56 (11) :2972-2978
[3]   PRODUCTION OF COLONY-STIMULATING FACTORS (CSFS) DURING INFECTION - SEPARATE DETERMINATIONS OF MACROPHAGE-CSF, GRANULOCYTE-CSF, GRANULOCYTE-MACROPHAGE-CSF, AND MULTI-CSF [J].
CHEERS, C ;
HAIGH, AM ;
KELSO, A ;
METCALF, D ;
STANLEY, ER ;
YOUNG, AM .
INFECTION AND IMMUNITY, 1988, 56 (01) :247-251
[4]  
CHEERS C, 1990, IMMUNOLOGY, V70, P411
[5]   INTERLEUKIN-6 INDUCED AT MUCOSAL SURFACES BY GRAM-NEGATIVE BACTERIAL-INFECTION [J].
DEMAN, P ;
VANKOOTEN, C ;
AARDEN, L ;
ENGBERG, I ;
LINDER, H ;
EDEN, CS .
INFECTION AND IMMUNITY, 1989, 57 (11) :3383-3388
[6]   STIMULATION OF ANTIBACTERIAL MACROPHAGE ACTIVITIES BY B-CELL STIMULATORY FACTOR-II (INTERLEUKIN-6) [J].
FLESCH, IEA ;
KAUFMANN, SHE .
INFECTION AND IMMUNITY, 1990, 58 (01) :269-271
[7]   ANTIBACTERIAL ACTIVITY OF RECOMBINANT MURINE BETA-INTERFERON [J].
FUJIKI, T ;
TANAKA, A .
INFECTION AND IMMUNITY, 1988, 56 (03) :548-551
[8]   INTERLEUKIN-6 PRODUCTION IN EXPERIMENTAL CEREBRAL MALARIA - MODULATION BY ANTICYTOKINE ANTIBODIES AND POSSIBLE ROLE IN HYPERGAMMAGLOBULINEMIA [J].
GRAU, GE ;
FREI, K ;
PIGUET, PF ;
FONTANA, A ;
HEREMANS, H ;
BILLIAU, A ;
VASSALLI, P ;
LAMBERT, PH .
JOURNAL OF EXPERIMENTAL MEDICINE, 1990, 172 (05) :1505-1508
[9]   TREATMENT OF MICE WITH HUMAN RECOMBINANT INTERLEUKIN-2 AUGMENTS RESISTANCE TO THE FACULTATIVE INTRACELLULAR PATHOGEN LISTERIA-MONOCYTOGENES [J].
HAAKFRENDSCHO, M ;
YOUNG, KM ;
CZUPRYNSKI, CJ .
INFECTION AND IMMUNITY, 1989, 57 (10) :3014-3021
[10]  
HACK CE, 1989, BLOOD, V74, P1704