Choy E H, Kingsley G H, Panayi G S
Rheumatology Unit, Guy's Hospital, London.
Br J Rheumatol. 1998 May;37(5):484-90. doi: 10.1093/rheumatology/37.5.484.
Monoclonal antibodies bind to their targets with high specificity and therefore have excellent potential as therapeutic agents. Biotechnological advances have allowed the production of large quantities of engineered monoclonal antibodies for therapeutic use. Recent research in rheumatoid arthritis has identified important mediators of synovitis. Monoclonal antibodies targeting these have been tested in clinical trials over the last decade. Anti-cytokine therapies, in particular anti-tumour necrosis factor alpha monoclonal antibodies, suppressed inflammation and produced rapid symptomatic improvement. Anti-lymphocyte monoclonal antibodies produced long-lasting disease suppression in animal models of rheumatoid arthritis. The use of depleting anti-lymphocyte monoclonal antibodies in rheumatoid arthritis had been disappointing as they did not penetrate the synovial joint in sufficient quantity to suppress disease without producing severe and protracted peripheral blood lymphopenia. Consequently, their use in rheumatoid arthritis had been abandoned. In contrast, clinical trials of non-depleting anti-CD4 monoclonal antibodies in rheumatoid arthritis showed that they could suppress synovitis. However, it remains unclear whether they could lead to prolonged disease improvement.
单克隆抗体以高特异性与其靶标结合,因此作为治疗剂具有巨大潜力。生物技术的进步使得能够生产大量用于治疗的工程化单克隆抗体。类风湿性关节炎的最新研究已经确定了滑膜炎的重要介质。在过去十年中,针对这些介质的单克隆抗体已在临床试验中进行了测试。抗细胞因子疗法,特别是抗肿瘤坏死因子α单克隆抗体,可抑制炎症并迅速改善症状。抗淋巴细胞单克隆抗体在类风湿性关节炎动物模型中产生了持久的疾病抑制作用。在类风湿性关节炎中使用消耗性抗淋巴细胞单克隆抗体一直令人失望,因为它们无法足够量地穿透滑膜关节以抑制疾病,同时又不会导致严重且持久的外周血淋巴细胞减少。因此,它们在类风湿性关节炎中的应用已被放弃。相比之下,类风湿性关节炎中非消耗性抗CD4单克隆抗体的临床试验表明,它们可以抑制滑膜炎。然而,它们是否能导致疾病长期改善仍不清楚。