Swetha Byravan, Harini Samarasinghe, Jack Shi Jie Yuan, Syed Haider Tahir, Arumugam Moorthy, Hasan Tahir
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引用次数: 0
Abstract
Introduction: IL-17 has been described as a pro-inflammatory cytokine that is relevant in the seronegative spondylarthritides with IL-17 targeted therapies being licensed for their treatment.There is evidence to demonstrate that IL-17 is found in RA joints and contributes to the pro-inflammatory cascade. This results in synovial hyperplasia and osteoclastogenesis thus causing joint destruction and bony erosions.
Areas covered: This review article summarizes trials that have studied the use of IL-17 targeted therapies in RA patients who have failed conventional synthetic disease-modifying therapy (C-DMARDS) and biologic DMARDS.
Expert opinion: The trials that have studied IL-17 inhibitors in RA patients have only shown a modest improvement in disease activity. In several trials, the primary endpoint was not achieved whilst in others, when comparing with existing licensed biologics for RA, did not demonstrate any superiority.Tissue Necrosis Factor-alpha (TNF-α) likely plays more of a pivotal role in the pathogenesis of RA with IL-17 having a synergistic effect. Therefore, in our opinion, IL-17 inhibitors as an independent therapy for RA are less likely to provide a cost-effective benefit. There may be scope to potentially combine it with TNF-α-inhibitors (TNF-i), but this requires further research especially with the potential concerns related to increased immunosuppression.
简介:IL-17被描述为一种促炎细胞因子,与血清阴性脊柱关节炎有关,IL-17靶向疗法已获得治疗许可。这导致滑膜增生和破骨细胞生成,从而引起关节破坏和骨质侵蚀:这篇综述文章总结了对传统合成疾病缓解疗法(C-DMARDS)和生物DMARDS治疗失败的RA患者使用IL-17靶向疗法的试验研究:IL-17抑制剂治疗RA患者的试验仅显示疾病活动略有改善。组织坏死因子-α(TNF-α)可能在 RA 的发病机制中起着更关键的作用,而 IL-17 具有协同作用。因此,我们认为,IL-17抑制剂作为独立疗法治疗RA不太可能带来成本效益。IL-17抑制剂有可能与TNF-α抑制剂(TNF-i)联合使用,但这需要进一步研究,特别是考虑到与免疫抑制增加有关的潜在问题。
期刊介绍:
Expert Opinion on Investigational Drugs (ISSN 1354-3784 [print], 1744-7658 [electronic]) is a MEDLINE-indexed, peer-reviewed, international journal publishing review articles and original papers on drugs in preclinical and early stage clinical development, providing expert opinion on the scope for future development.
The Editors welcome:
Reviews covering preclinical through to Phase II data on drugs or drug classes for specific indications, and their potential impact on future treatment strategies
Drug Evaluations reviewing the clinical and pharmacological data on a particular drug
Original Research papers reporting the results of clinical investigations on agents that are in Phase I and II clinical trials
The audience consists of scientists, managers and decision-makers in the pharmaceutical industry, and others closely involved in R&D.