Ouboussad Lylia, Burska Agata N, Melville Andrew, Buch Maya H
Leeds Institute of Rheumatic and Musculoskeletal Medicine, University of Leeds, Leeds, United Kingdom.
NIHR Leeds Biomedical Research Centre, Leeds Teaching Hospitals NHS Trust, Leeds, United Kingdom.
Front Med (Lausanne). 2019 Mar 19;6:45. doi: 10.3389/fmed.2019.00045. eCollection 2019.
The treatment of rheumatoid arthritis (RA) has been transformed with the introduction of biologic disease modifying anti-rheumatic drugs (bDMARD) and more recently, targeted synthetic DMARD (tsDMARD) therapies in the form of janus-kinase inhibitors. Nevertheless, response to these agents varies such that a trial and error approach is adopted; leading to poor patient quality of life, and long-term outcomes. There is thus an urgent need to identify effective biomarkers to guide treatment selection. A wealth of research has been invested in this field but with minimal progress. Increasingly recognized is the importance of evaluating synovial tissue, the primary site of RA, as opposed to peripheral blood-based investigation. In this mini-review, we summarize the literature supporting synovial tissue heterogeneity, the conceptual basis for stratified therapy. This includes recognition of distinct synovial pathobiological subtypes and associated molecular pathways. We also review synovial tissue studies that have been conducted to evaluate the effect of individual bDMARD and tsDMARD on the cellular and molecular characteristics, with a view to identifying tissue predictors of response. Initial observations are being brought into the clinical trial landscape with stratified biopsy trials to validate toward implementation. Furthermore, development of tissue based omics technology holds still more promise in advancing our understanding of disease processes and guiding future drug selection.
随着生物性病情改善抗风湿药物(bDMARD)的引入,以及最近以 Janus 激酶抑制剂形式出现的靶向合成 DMARD(tsDMARD)疗法的应用,类风湿关节炎(RA)的治疗发生了变革。然而,对这些药物的反应各不相同,因此采用了试错法;这导致患者生活质量低下和长期预后不佳。因此,迫切需要确定有效的生物标志物来指导治疗选择。该领域已投入大量研究,但进展甚微。越来越多的人认识到评估滑膜组织(RA 的主要病变部位)的重要性,而不是基于外周血的研究。在这篇小型综述中,我们总结了支持滑膜组织异质性的文献,这是分层治疗的概念基础。这包括识别不同的滑膜病理生物学亚型和相关分子途径。我们还回顾了为评估单个 bDMARD 和 tsDMARD 对细胞和分子特征的影响而进行的滑膜组织研究,以期确定反应的组织预测指标。初步观察结果正通过分层活检试验引入临床试验领域,以验证其是否可用于实际应用。此外,基于组织的组学技术的发展在增进我们对疾病过程的理解和指导未来药物选择方面仍有更大的前景。