IMPAIRED IMMUNE AND ACUTE-PHASE RESPONSES IN INTERLEUKIN-6-DEFICIENT MICE

被引:1531
作者
KOPF, M
BAUMANN, H
FREER, G
FREUDENBERG, M
LAMERS, M
KISHIMOTO, T
ZINKERNAGEL, R
BLUETHMANN, H
KOHLER, G
机构
[1] ROSWELL PK CANC INST, DEPT MOLEC & CELLULAR BIOL, BUFFALO, NY 14263 USA
[2] UNIV ZURICH, INST EXPTL IMMUNOL, ZURICH, SWITZERLAND
[3] HOFFMANN LA ROCHE AG, DEPT BIOL, CH-4002 BASEL, SWITZERLAND
[4] OSAKA UNIV, SCH MED, DEPT MED 3, OSAKA, OSAKA 565, JAPAN
关键词
D O I
10.1038/368339a0
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
INTERLEUKIN-6 (IL-6) is a multifunctional cytokine that regulates various aspects of the immune response, acute-phase reaction and haematopoiesis (for reviews see refs 1, 2). In vitro, leukaemia inhibitory factor, oncostatin M, ciliary neurotrophic factor and interleukin-ll display overlapping activities with IL-6. This functional redundancy may be explained by the interactions of specific binding receptors with a common signal-transducing receptor (gp130) (for reviews see refs 3, 4). To elucidate the unique function of IL-6 in vivo, we have disrupted the IL-6 gene by homologous recombination. IL-6-deficient mice develop normally. They fail to control efficiently vaccinia virus and infection with Listeria mono-cytogenes, a facultative intracellular bacterium. The T-cell-dependent antibody response against vesicular stomatitis virus is impaired. Further, the inflammatory acute-phase response after tissue damage or infection is severely compromised, whereas it is only moderately affected after challenge with lipopolysaccharide. We conclude that IL-6 production induced by injury or infection is an important in vivo SOS signal which coordinates activities of liver cells, macrophages and lymphocytes.
引用
收藏
页码:339 / 342
页数:4
相关论文
共 30 条
  • [1] BAUMANN H, 1988, METHOD ENZYMOL, V163, P566
  • [2] MOUSE ALPHA-1-PROTEASE INHIBITOR IS NOT AN ACUTE PHASE REACTANT
    BAUMANN, H
    LATIMER, JJ
    GLIBETIC, MD
    [J]. ARCHIVES OF BIOCHEMISTRY AND BIOPHYSICS, 1986, 246 (01) : 488 - 493
  • [3] BECKERMAN KP, 1993, J IMMUNOL, V150, P888
  • [4] BINDER D, 1991, J IMMUNOL, V146, P4301
  • [5] Blanden R V, 1972, Scand J Immunol, V1, P379, DOI 10.1111/j.1365-3083.1972.tb03304.x
  • [6] MULTIPLE DEFECTS OF IMMUNE CELL-FUNCTION IN MICE WITH DISRUPTED INTERFERON-GAMMA GENES
    DALTON, DK
    PITTSMEEK, S
    KESHAV, S
    FIGARI, IS
    BRADLEY, A
    STEWART, TA
    [J]. SCIENCE, 1993, 259 (5102) : 1739 - 1742
  • [7] DING AH, 1988, J IMMUNOL, V141, P2407
  • [8] DOHERTY PC, 1992, ANNU REV IMMUNOL, V10, P123
  • [9] GREGORY SH, 1993, J IMMUNOL, V150, P2901
  • [10] PRIMARY ANTIBODY-RESPONSES TO A WELL-DEFINED AND UNIQUE HAPTEN ARE NOT ENHANCED BY PREIMMUNIZATION WITH CARRIER - ANALYSIS IN A VIRAL MODEL
    GUPTA, SC
    HENGARTNER, H
    ZINKERNAGEL, RM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1986, 83 (08) : 2604 - 2608