Greenwald R A
Long Island Jewish Medical Center/Albert Einstein College of Medicine/School of Medicine and School of Dental Medicine, State University of New York at Stony Brook.
J Clin Rheumatol. 1995 Jun;1(3):185-9. doi: 10.1097/00124743-199506000-00011.
Several clinical trials have been conducted in the past 3 years using minocycline as an anti-inflammatory agent for rheumatoid arthritis (RA), Depending on one's viewpoint, these trials have or have not shown a mild beneficial effect on conventional RA parameters of inflammation. In the context of currently available anti-inflammatory therapy, the magnitude of the reported effects would not seem to justify additional large scale trials. There is, however, compelling basic science data as well as preliminary clinical data, suggesting that certain tetracyclines may have a valuable role to play in treatment of RA. There is even reason to believe that such an agent could be the Holy Grail of rheumatology, namely the drug that prevents connective tissue degradation in destructive arthritides. This concept is based on the properties of tetracyclines as inhibitors of matrix metalloproteinases. In this article, the properties of the tetracyclines in this regard are reviewed, and concepts are suggested for the design of a trial addressing the unique properties of these drugs.
在过去3年里,已经开展了几项使用米诺环素作为类风湿性关节炎(RA)抗炎药的临床试验。根据个人观点,这些试验对传统的RA炎症参数显示或未显示出轻微的有益效果。在目前可用的抗炎治疗背景下,所报道效果的程度似乎不足以证明有必要进行更多大规模试验。然而,有令人信服的基础科学数据以及初步临床数据表明,某些四环素类药物可能在RA治疗中发挥重要作用。甚至有理由相信,这样一种药物可能是风湿病学的圣杯,即能够防止破坏性关节炎中结缔组织降解的药物。这一概念基于四环素类药物作为基质金属蛋白酶抑制剂的特性。在本文中,将对四环素类药物在这方面的特性进行综述,并提出针对这些药物独特特性设计试验的概念。