Essential involvement of interleukin-8 in neutrophil recruitment in rabbits with acute experimental arthritis induced by lipopolysaccharide and interleukin-1.

Lymphokine and cytokine research Pub Date : 1994-04-01
T Akahoshi, H Endo, H Kondo, S Kashiwazaki, T Kasahara, N Mukaida, A Harada, K Matsushima
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Abstract

Rheumatoid arthritis and related inflammatory joint diseases are characterized by massive infiltration of polymorphonuclear cells (PMN) into inflamed joints. Interleukin-8 (IL-8) has recently been identified as a leukocyte chemotactic and activating factor produced by activated tissue cells as well as monocytes/macrophages. Examination was made of the involvement of IL-8 in acute arthritis induced by injecting lipopolysaccharide (LPS) or interleukin-1 alpha (IL-1 alpha) into the joints of rabbits. The neutralizing antibody to rabbit IL-8 blocked almost completely the infiltration of PMN into the joints and provided protection from damage to tissue in the early phase of inflammation induced by LPS or IL-1 alpha. Mononuclear cell infiltration observed later was not inhibited by this antibody. This is the first paper to clearly demonstrate that IL-8 is an essential and major mediator determining whether PMN infiltration will occur in the early phase of experimental acute arthritis.

白细胞介素-8在脂多糖和白细胞介素-1诱导的兔急性实验性关节炎中性粒细胞募集中的重要作用。
类风湿关节炎及相关炎症性关节疾病的特征是炎症关节内大量多形核细胞(PMN)浸润。白细胞介素-8 (IL-8)最近被确定为一种白细胞趋化和激活因子,由活化的组织细胞以及单核/巨噬细胞产生。采用关节内注射脂多糖(LPS)或白细胞介素-1 α (IL-1 α),观察IL-8在兔急性关节炎中的作用。兔IL-8中和抗体几乎完全阻断PMN向关节的浸润,并在LPS或IL-1 α诱导的炎症早期对组织的损伤提供保护。随后观察到的单核细胞浸润不受该抗体的抑制。这是第一篇明确证明IL-8是决定实验性急性关节炎早期是否会发生PMN浸润的重要和主要介质的论文。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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