Szekanecz Zoltán, Gáspár Levente, Koch Alisa Erika
Division of Rheumatology, Third Department of Medicine, University of Debrecen Medical and Health Sciences Center, Debrecen, H-4004, Hungary.
Front Biosci. 2005 May 1;10:1739-53. doi: 10.2741/1657.
Endothelial cells lining the lumina of blood vessels are involved in leukocyte extravasation underlying inflammatory states, such as rheumatoid arthritis (RA). New vessel formation, termed angiogenesis, is also crucial for leukocyte extravasation during inflammatory synovitis. The outcome of neovascularization in the RA synovium is highly dependent on the balance or imbalance between angiogenic mediators and inhibitors. There have been several attempts to therapeutically interfere with the cellular and molecular mechanisms underlying RA-associated neovascularization. Most studies have been performed using animal models of arthritis. In addition, a limited number of human clinical trials gave promising results. In this review, authors summarize some relevant information on those angiogenic and angiostatic agents, which have also been studied in context with RA. In addition, further perspectives of anti-angiogenic therapy in arthritis are also discussed. Specific targeting of angiogenesis may be useful in the future management of various inflammatory, as well as malignant, diseases.
血管腔内壁的内皮细胞参与了诸如类风湿性关节炎(RA)等炎症状态下的白细胞渗出过程。新血管形成,即血管生成,对于炎症性滑膜炎期间的白细胞渗出也至关重要。RA滑膜中新生血管形成的结果高度依赖于血管生成介质与抑制剂之间的平衡或失衡。人们已多次尝试从治疗上干预RA相关新生血管形成的细胞和分子机制。大多数研究是使用关节炎动物模型进行的。此外,少数人体临床试验也给出了有前景的结果。在本综述中,作者总结了一些与这些血管生成和血管生成抑制因子相关的信息,这些因子也在RA的背景下进行了研究。此外,还讨论了抗血管生成疗法在关节炎中的进一步前景。血管生成的特异性靶向在未来各种炎症性疾病以及恶性疾病的治疗中可能会有用。