Division of Rheumatology, Istituto G Pini, Piazza C. Ferrari, 1, 20122, Milan, Italy.
Clin Rev Allergy Immunol. 2014 Aug;47(1):6-16. doi: 10.1007/s12016-013-8359-x.
Biological drugs targeting pro-inflammatory or co-stimulatory molecules or depleting lymphocyte subsets made a revolution in rheumatoid arthritis (RA) treatment. Their comparable efficacy in clinical trials raised the point of the heterogeneity of RA pathogenesis, suggesting that we are dealing with a syndrome rather than with a single disease. Several tumor necrosis factor-alpha (TNF-α) blockers are available, and a burning question is whether they are biosimilar or not. The evidence of diverse biological effects in vitro is in line with the fact that a lack of efficacy to one TNF-α agent does not imply a non-response to another one. As proteins, biologicals are potentially immunogenic. It has been recently raised that anti-drug antibodies (ADA) may affect their bioavailability and eventually the clinical efficacy through local formation of immune complexes and directly by preventing the interaction between the drug and TNF-α. Regular monitoring of drug and ADA levels appears the best way to tailor anti-TNF-α therapies. Owing to the pleiotropic characteristics of the target, anti-TNF-α blockers may affect several mechanisms beyond rheumatoid synovitis. As TNF-α plays a pivotal role in the induction of early atherosclerosis, treatment with TNF-inhibitors may modulate cholesterol handling, in particular, cholesterol efflux from macrophages. Side effects are a major issue because of the systemic TNF-α blocking action. The efficacy of an anti-C5 monoclonal antibody fused to a peptide targeting inflamed synovia in experimental arthritis opened the way for new strategies: Homing to the synovium of molecules neutralizing TNF would allow to maximize the therapeutic action avoiding the side effects.
针对促炎或共刺激分子或耗竭淋巴细胞亚群的生物药物在类风湿关节炎(RA)治疗中引发了一场革命。临床试验中它们相当的疗效提出了 RA 发病机制异质性的观点,表明我们正在处理一种综合征而不是单一疾病。有几种肿瘤坏死因子-α(TNF-α)阻滞剂可用,一个热门问题是它们是否具有生物相似性。体外多种生物学效应的证据与以下事实相符,即一种 TNF-α 药物无效并不意味着对另一种药物无反应。作为蛋白质,生物制剂具有潜在的免疫原性。最近有人提出,抗药物抗体(ADA)可能会通过局部形成免疫复合物并直接阻止药物与 TNF-α 相互作用,从而影响它们的生物利用度并最终影响临床疗效。定期监测药物和 ADA 水平似乎是定制抗 TNF-α 治疗的最佳方法。由于靶标的多效性特征,抗 TNF-α 阻滞剂可能会影响类风湿关节炎滑膜以外的几种机制。由于 TNF-α 在早期动脉粥样硬化的诱导中起关键作用,因此 TNF 抑制剂的治疗可能会调节胆固醇的处理,特别是从巨噬细胞中排出胆固醇。由于全身 TNF-α 阻断作用,副作用是一个主要问题。在实验性关节炎中,与靶向炎症滑膜的肽融合的抗 C5 单克隆抗体的疗效为新策略开辟了道路:针对中和 TNF 的分子向滑膜归巢将允许在避免副作用的情况下最大限度地发挥治疗作用。