Akahoshi T, Endo H, Kondo H, Kashiwazaki S, Kasahara T, Mukaida N, Harada A, Matsushima K
Department of Internal Medicine, Kitasato University School of Medicine, Japan.
Lymphokine Cytokine Res. 1994 Apr;13(2):113-6.
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.
类风湿性关节炎及相关炎性关节疾病的特点是多形核细胞(PMN)大量浸润到发炎的关节中。白细胞介素-8(IL-8)最近被确定为一种由活化的组织细胞以及单核细胞/巨噬细胞产生的白细胞趋化和激活因子。研究了IL-8在向兔关节注射脂多糖(LPS)或白细胞介素-1α(IL-1α)诱导的急性关节炎中的作用。抗兔IL-8中和抗体几乎完全阻断了PMN向关节的浸润,并在LPS或IL-1α诱导的炎症早期保护组织免受损伤。该抗体并未抑制随后观察到的单核细胞浸润。这是第一篇明确证明IL-8是决定实验性急性关节炎早期PMN浸润是否会发生的关键和主要介质的论文。