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关节炎中炎症与破坏机制的解偶联。

Uncoupling of inflammatory and destructive mechanisms in arthritis.

作者信息

van den Berg W B

机构信息

Department of Rheumatology, University Medical Center, Nijmegen, The Netherlands.

出版信息

Semin Arthritis Rheum. 2001 Apr;30(5 Suppl 2):7-16. doi: 10.1053/sarh.2001.23704.

Abstract

OBJECTIVE

To update clinicians on recent advances in the differentiation of the mechanisms of inflammation and cartilage destruction in the pathogenesis of rheumatoid arthritis (RA).

METHODS

We present analysis of recent published literature and abstracts that elucidates the independent actions of pivotal proinflammatory cytokines. These experimental data provide the framework for understanding the uncoupling of destructive and inflammatory mechanisms in arthritis.

RESULTS

Tumor necrosis factor-alpha (TNF-alpha) is an important mediator in the inflammation that occurs in RA. Interleukin-1 (IL-1) has a dominant effect on cartilage destruction that occurs later in the disease process. TNF-independent IL-1 production occurs in many RA model situations. Cytokine balance determines the erosive nature of the disease.

CONCLUSION

IL-1 is at least as important as TNF-alpha in promoting the disease process. The pathways by which the inflammatory and destructive changes occur suggest that targeted anticytokine intervention will arrest the cartilage damage that occurs in patients with RA.

摘要

目的

向临床医生介绍类风湿关节炎(RA)发病机制中炎症和软骨破坏机制分化的最新进展。

方法

我们对近期发表的文献和摘要进行分析,阐明关键促炎细胞因子的独立作用。这些实验数据为理解关节炎中破坏机制和炎症机制的解偶联提供了框架。

结果

肿瘤坏死因子-α(TNF-α)是RA中发生的炎症的重要介质。白细胞介素-1(IL-1)对疾病后期发生的软骨破坏具有主导作用。在许多RA模型情况下会出现不依赖TNF的IL-1产生。细胞因子平衡决定了疾病的侵蚀性。

结论

IL-1在促进疾病进程中至少与TNF-α一样重要。炎症和破坏变化发生的途径表明,靶向抗细胞因子干预将阻止RA患者发生的软骨损伤。

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