Inhibition of neutrophil-mediated acute inflammatory injury by an antibody against interleukin-8 (IL-8)

被引:0
|
作者
Mukaida, N
Matsumoto, T
Yokoi, K
Harada, A
Matsushima, K
机构
[1] Kanazawa Univ, Canc Res Inst, Dept Mol Pharmacol, Kanazawa, Ishikawa 9200934, Japan
[2] Kanazawa Univ, Dept Neurosurg, Kanazawa, Ishikawa 9200934, Japan
[3] Kanazawa Univ, Dept Surg 1, Kanazawa, Ishikawa 9200934, Japan
[4] Kanazawa Univ, Sch Med, Dept Hyg, Kanazawa, Ishikawa 9200934, Japan
[5] Univ Tokyo, Sch Med, Dept Mol Prevent Med, Bunkyo Ku, Tokyo 1130033, Japan
关键词
interleukin-8; neutrophil; acute inflammation; cerebral reperfusion injury; acute respiratory distress syndrome;
D O I
暂无
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
Chemokines are a family of cytokines regulating the migration and functions of leukocytes in a cell-type specific manner. A prototype of C-X-C chemokines, interleukin-X (IL-8), chemoattracts and activates neutrophils in vitro, and IL-8 concentrations in body fluids are markedly increased in several neutrophil-mediated acute inflammation. Moreover, we previously reported that the administration of a neutralizing antibody to IL-8 prevented neutrophil mediated tissue injury, as well as neutrophil infiltration, in several animal disease models. These observations implicate IL-8 as a major mediator of neutrophil-mediated tissue injury. Furthermore, we recently showed that an anti-IL-8 antibody effectively prevented two models that are very relevant to clinical situations; endotoxemia-induced acute respiratory distress syndrome (ARDS)-like lung injury and cerebral reperfusion injury. These results raise the possibility that IL-8 is a novel target for therapeutic intervention in neutrophil-mediated acute inflammation.
引用
收藏
页码:S151 / S157
页数:7
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