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在大鼠体内用白细胞介素-1进行治疗可降低抗原诱导性关节炎的严重程度和持续时间。

In vivo treatment with IL-1 reduces the severity and duration of antigen-induced arthritis in rats.

作者信息

Jacobs C, Young D, Tyler S, Callis G, Gillis S, Conlon P J

机构信息

Department of Cellular Immunology, Immunex Corporation, Seattle, WA 98101.

出版信息

J Immunol. 1988 Nov 1;141(9):2967-74.

PMID:3262673
Abstract

IL-1 has been implicated in the pathogenesis of arthritis. Although IL-1 injected in vivo into normal joints results in a transient inflammatory reaction, we have shown that three weekly repetitive injections of IL-1 do not produce a progressive inflammatory condition suggestive of chronic arthritis. In fact, priming normal joints with three weekly IL-1 intraarticular injections results in a significant reduction in joint swelling and diminished histopathologic alterations/lesions caused by subsequent methylated BSA-induced arthritis. Similarly, post treatment with IL-1 intraarticular injection after arthritis induction reduced arthritic swelling and joint injury if IL-1 was given during the developing stage of arthritis. Our results suggest that IL-1 might limit arthritic inflammation and progressive cartilage destruction through an, as yet, undetermined mechanism(s). Further in vivo investigations are required to determine the therapeutic utility of IL-1 in reducing early arthritic inflammation.

摘要

白细胞介素-1(IL-1)已被认为与关节炎的发病机制有关。虽然将IL-1体内注射到正常关节会导致短暂的炎症反应,但我们已经表明,每周三次重复注射IL-1不会产生提示慢性关节炎的进行性炎症状态。事实上,每周三次关节内注射IL-1对正常关节进行预处理,可显著减轻关节肿胀,并减少随后甲基化牛血清白蛋白诱导的关节炎所引起的组织病理学改变/损伤。同样,如果在关节炎发展阶段给予IL-1关节内注射进行治疗后,可减轻关节炎肿胀和关节损伤。我们的结果表明,IL-1可能通过一种尚未确定的机制来限制关节炎炎症和进行性软骨破坏。需要进一步的体内研究来确定IL-1在减轻早期关节炎炎症方面的治疗效用。

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