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炎症性骨损伤的分子机制:新兴的治疗靶点

Molecular mechanisms of inflammatory bone damage: emerging targets for therapy.

作者信息

Herman Sonja, Krönke Gerhard, Schett Georg

机构信息

Department of Internal Medicine 3, University of Erlangen-Nuremberg, Krankenhausstrasse 12, D-91054 Erlangen, Germany.

出版信息

Trends Mol Med. 2008 Jun;14(6):245-53. doi: 10.1016/j.molmed.2008.04.001. Epub 2008 May 9.

Abstract

Chronic inflammatory bone diseases, such as rheumatoid arthritis (RA), ankylosing spondylitis and periodontal disease, demonstrate the major impact of chronic inflammation on both bone metabolism and bone architecture. During the past decade, scientists have gained increasing insight into the link between inflammation and bone. As a result of new discoveries about the molecular mechanisms of inflammatory bone loss, several molecules have been identified that are attractive and novel targets for the treatment of inflammatory bone loss. These novel therapeutic approaches include anti-tumor necrosis factor (TNF)-alpha blocking agents, neutralizing antibodies against certain pro-inflammatory cytokines, such as interleukin (IL)-6 and IL-17, and a set of other promising targets that still require extensive research, such as the Wnt signaling network.

摘要

慢性炎症性骨病,如类风湿性关节炎(RA)、强直性脊柱炎和牙周病,显示出慢性炎症对骨代谢和骨结构的重大影响。在过去十年中,科学家们对炎症与骨之间的联系有了越来越深入的了解。由于对炎症性骨丢失分子机制的新发现,已确定了几种分子,它们是治疗炎症性骨丢失有吸引力的新靶点。这些新的治疗方法包括抗肿瘤坏死因子(TNF)-α阻断剂、针对某些促炎细胞因子(如白细胞介素(IL)-6和IL-17)的中和抗体,以及一组仍需广泛研究的其他有前景的靶点,如Wnt信号网络。

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