Schorlemmer H U, Kanzy E J, Langner K D, Kurrle R
Research Laboratories of Behringwerke AG, Marburg/Lahn, Germany.
Agents Actions. 1993;39 Spec No:C113-6. doi: 10.1007/BF01972739.
Given the role of IL-1 in inflammation and in autoimmune diseases, studies were designed to examine the ability of IL-1 receptor (IL-1-R) to suppress inflammation in a model of chronic degenerative joint disease of adjuvant arthritis (AA) in Lewis rats and to suppress the development of a systemic lupus erythematosus (SLE)-like disease in MRL/lpr mice. IL-1-R was able to prevent the onset of the AA and, even if therapy started after the establishment of AA, the cytokine receptor was still able to reduce the degree of chronic inflammation and arrested its progress. Treating MRL/lpr mice with IL-1-R resulted in a decrease in the amount of autoantibodies and inhibited joint inflammation. Even in the established disease IL-1-R could reduce rheumatoid factors (RF) and autoantibodies, and the signs of a polyarthritis were inhibited.
鉴于白细胞介素-1(IL-1)在炎症和自身免疫性疾病中的作用,研究旨在检测白细胞介素-1受体(IL-1-R)在佐剂性关节炎(AA)慢性退行性关节疾病模型中抑制炎症的能力,以及在MRL/lpr小鼠中抑制系统性红斑狼疮(SLE)样疾病发展的能力。IL-1-R能够预防AA的发作,即使在AA形成后开始治疗,细胞因子受体仍能够减轻慢性炎症的程度并阻止其进展。用IL-1-R治疗MRL/lpr小鼠可使自身抗体量减少并抑制关节炎症。即使在疾病已确立的情况下,IL-1-R也可降低类风湿因子(RF)和自身抗体,并抑制多关节炎的症状。