Rheumatology Department, Military Hospital of Tunis, Tunis, Tunisia.
Internal Medicine Department, Military Hospital of Tunis, Tunis, Tunisia.
Curr Rev Clin Exp Pharmacol. 2021;16(3):235-238. doi: 10.2174/1574884715666200917102055.
Over the years, drug monitoring-such as Anti-Drug Antibodies (ADA) dosage- has witnessed major transformations. In fact, ADA are more and more used in rheumatology and gastro-enterology in monitoring chronic inflammatory disease therapeutic response. The main purpose of those researches is to produce less immunogenic drugs and, in consequences, to improve tolerance and efficiency since immunogenicity of those drugs still is the main constraint to their long-term use. The aim of this review was to highlight anti-drug-antibodies potential effects on the pharmacokinetics and bioavailability of biotherapies as well as their clinical implications.
For this purpose, we collected and summarized published data on PubMed using keywords "Biologics, Rheumatoid Arthritis, Spondyloarthritis, Crohn disease, Anti-drug antibodies, residual rate, immunogenicity, efficacy, tolerance". The time-period selected for this study was 2000-2019.
Anti-Drug-antibodies decrease the pharmaco-availability of drugs and, in consequences, its efficiency and high risk of refractory diseases and side effects.
Recent literature is consistent with the fact that drug monitoring using ADA dosage coupled with residual drug concentration offers reliable options to comfort practitioner' therapeutic management decisions. This is particularly interesting in failure of treatment or in side effects onset situations.
多年来,药物监测——如抗药物抗体 (ADA) 剂量——已经发生了重大转变。事实上,ADA 越来越多地用于风湿病学和胃肠病学,以监测慢性炎症性疾病的治疗反应。这些研究的主要目的是生产免疫原性更低的药物,从而提高耐受性和疗效,因为这些药物的免疫原性仍然是其长期使用的主要限制。本文的目的是强调抗药物抗体对生物疗法的药代动力学和生物利用度的潜在影响及其临床意义。
为此,我们使用关键词“生物制剂、类风湿关节炎、脊柱关节炎、克罗恩病、抗药物抗体、残留率、免疫原性、疗效、耐受性”在 PubMed 上收集和总结已发表的数据。本研究选择的时间段为 2000-2019 年。
抗药物抗体降低了药物的药代动力学可用性,从而降低了其疗效和发生难治性疾病和副作用的高风险。
最近的文献与以下事实一致,即使用 ADA 剂量和残留药物浓度进行药物监测为临床医生的治疗管理决策提供了可靠的选择。在治疗失败或出现副作用的情况下,这一点尤其有趣。