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Synovial Tissue Heterogeneity in Rheumatoid Arthritis and Changes With Biologic and Targeted Synthetic Therapies to Inform Stratified Therapy

机译:类风湿性关节炎的滑膜组织异质性和生物学和靶向合成疗法的变化,以通知分层治疗

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The treatment of rheumatoid arthritis 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 summarise 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 towards implementation. Furthermore, development of tissue based omics technology holds still more promise in advancing our understanding of disease processes and guiding future drug selection.
机译:通过引入生物疾病改性抗风湿药物(BDMARD)和更近期,靶向合成的DMARD(TSDMARD)疗法以Janus-激酶抑制剂的形式进行转化为类风湿性关节炎。然而,对这些代理商的反应变化,使得采用试验和误差方法;导致患者生活质量差和长期结果。因此,迫切需要识别有效的生物标志物以指导治疗选择。这一领域已经投入了丰富的研究,但进展最少。越来越认识到是评估滑膜组织,RA的原始部位的重要性,而不是基于外周血的调查。在这个迷你审查中,我们总结了支持滑膜组织异质性的文献,分层治疗的概念依据。这包括识别不同的滑膜病原体亚型和相关分子途径。我们还审查了在进行的滑膜组织研究,以评估单个BDMARD和TSDMARD对细胞和分子特性的影响,以鉴定响应的组织预测因子。初步观察是通过分层的活检试验进入临床试验景观,以验证实施。此外,基于组织的OMICS技术的发展在推进我们对疾病过程的理解和指导未来的药物选择方面仍然存在更多的承诺。

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