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Role of tumour necrosis factor α in experimental arthritis: separate activity of interleukin 1β in chronicity and cartilage destruction

机译:肿瘤坏死因子α在实验性关节炎中的作用:白介素1β在慢性和软骨破坏中的独立活性

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摘要

Chronic arthritis is characterised by persistent joint inflammation and concomitant joint destruction. Using murine arthritis models and neutralising antibodies as well as cytokine specific knockout conditions, it was found that tumour necrosis factor α (TNFα) is important in early joint swelling. Membrane bound TNFα is sufficient to drive this aspect of inflammation as well as the acute cellular infiltrate in the synovial tissue. Interleukin 1 (IL1) is not necessarily a dominant cytokine in early joint swelling, but has a pivotal role in sustained cellular infiltration and erosive cartilage damage. TNFα independent IL1 production is a prominent feature in murine arthritis models. These observations provide evidence for potential uncoupling of joint inflammation and erosive changes, implying that both cytokines need to be targeted to achieve optimal treatment.

机译:慢性关节炎的特征在于持续的关节发炎和伴随的关节破坏。使用鼠关节炎模型和中和抗体以及特定的细胞因子敲除条件,发现肿瘤坏死因子α(TNFα)在早期关节肿胀中很重要。膜结合的TNFα足以驱动该方面的炎症以及滑膜组织中的急性细胞浸润。白细胞介素1(IL1)不一定是早期关节肿胀的主要细胞因子,但在持续的细胞浸润和糜烂性软骨损伤中起关键作用。 TNFα依赖性IL1的产生是鼠关节炎模型的显着特征。这些观察结果为关节炎症和糜烂变化的潜在解耦提供了证据,这意味着需要针对这两种细胞因子来实现最佳治疗。

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