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

被引:1530
|
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.
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页码:339 / 342
页数:4
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