Rheumatology Division, School of Medicine, University of São Paulo, Rua Tabapuã, 1554 ap 1001, 04533-005, São Paulo, Brazil.
Clin Rheumatol. 2010 May;29(5):451-5. doi: 10.1007/s10067-009-1352-3. Epub 2010 Jan 27.
Osteoarthritis (OA) is the most common joint disorder worldwide, and it has an enormous socioeconomic impact both in the United States and throughout the world. The degree of articular inflammation is usually associated with the disease's progression, indicating that this process could contribute to articular damage. IL-1 beta and anti-TNF alpha are the two major cytokines players in the physiopathology of OA. Hence, we aimed to review the current literature on the effects of IL-1 and TNF-alpha neutralization as a new OA therapy. In vitro and experimental models showed a reduction in cartilage destruction with IL-1 inhibition therapy by IL-1 receptor antagonists (IL-1Ra). Despite this favorable evidence in animal models, studies on the inhibition of IL-1R in humans are still scarce. Although there is clear evidence that TNF-alpha plays a role in the pathophysiology of OA, only a few experimental trials have investigated the efficacy of blocking this pro-inflammatory cytokine in the treatment of OA. So far, the few studies available in humans using anti-TNF-alpha and IL-1 receptor antagonist are not remarkable, suggesting that further investigation and new therapeutic approaches are needed.
骨关节炎(OA)是全球最常见的关节疾病,它对美国和全世界都有巨大的社会经济影响。关节炎症的程度通常与疾病的进展有关,这表明这个过程可能导致关节损伤。IL-1β 和抗 TNF-α 是 OA 病理生理学中的两种主要细胞因子。因此,我们旨在回顾关于 IL-1 和 TNF-α 中和作为一种新的 OA 治疗的当前文献。体外和实验模型显示,IL-1 受体拮抗剂(IL-1Ra)抑制 IL-1 可减少软骨破坏。尽管在动物模型中有明确的证据,但关于人类 IL-1R 抑制的研究仍然很少。尽管有明确的证据表明 TNF-α 在 OA 的病理生理学中起作用,但只有少数实验性试验研究了阻断这种促炎细胞因子在 OA 治疗中的疗效。到目前为止,在人类中使用抗 TNF-α 和 IL-1 受体拮抗剂的少数研究并不显著,这表明需要进一步的研究和新的治疗方法。