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环孢素A对大鼠链球菌细胞壁诱导的关节炎和肝肉芽肿的抑制作用。

Inhibition by cyclosporin A of streptococcal cell wall-induced arthritis and hepatic granulomas in rats.

作者信息

Yocum D E, Allen J B, Wahl S M, Calandra G B, Wilder R L

出版信息

Arthritis Rheum. 1986 Feb;29(2):262-73. doi: 10.1002/art.1780290215.

Abstract

We investigated the effect of cyclosporin A, an inhibitor of T helper/inducer lymphocyte activation, on the development of streptococcal cell wall-induced arthritis and hepatic granulomas in female LEW/N rats. Continuous daily treatment with cyclosporin A, begun either 24 hours before or 7-12 days after streptococcal cell wall administration and continued for 6 weeks, resulted in significant inhibition of the chronic proliferative, erosive synovitis and total inhibition of hepatic granuloma formation. When cyclosporin A was stopped at 6 weeks, its effects continued for at least another 5 weeks, demonstrating long-term benefit without continued administration of the drug. In contrast, therapy given only during the acute phases of the experimental disease (days 1-12) did not inhibit the development of chronic disease. Cyclosporin A had no apparent effects on streptococcal cell wall antigen distribution or persistence in tissues. These data provide additional evidence of an important role for the T helper/inducer lymphocyte in the experimental model and suggest that cyclosporin A may be a useful probe in defining molecular and cellular processes involved in chronic proliferative and erosive synovitis.

摘要

我们研究了T辅助/诱导淋巴细胞激活抑制剂环孢素A对雌性LEW/N大鼠链球菌细胞壁诱导的关节炎和肝肉芽肿形成的影响。在给予链球菌细胞壁前24小时或给药后7 - 12天开始,持续每日用环孢素A治疗6周,可显著抑制慢性增殖性、侵蚀性滑膜炎,并完全抑制肝肉芽肿形成。当环孢素A在6周时停药,其作用至少持续另外5周,表明无需持续给药即可获得长期益处。相比之下,仅在实验性疾病急性期(第1 - 12天)给予治疗并不能抑制慢性疾病的发展。环孢素A对链球菌细胞壁抗原在组织中的分布或持续存在没有明显影响。这些数据为T辅助/诱导淋巴细胞在该实验模型中的重要作用提供了额外证据,并表明环孢素A可能是确定参与慢性增殖性和侵蚀性滑膜炎的分子和细胞过程的有用探针。

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