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骨关节炎的疾病修饰治疗策略:现状与未来方向。

Disease-modifying therapeutic strategies in osteoarthritis: current status and future directions.

机构信息

Department of Biological Sciences, College of Natural Sciences, Seoul National University, Seoul, 08826, South Korea.

Center for RNA Research, Institute for Basic Science, Seoul, 08826, South Korea.

出版信息

Exp Mol Med. 2021 Nov;53(11):1689-1696. doi: 10.1038/s12276-021-00710-y. Epub 2021 Nov 30.

Abstract

Osteoarthritis (OA) is the most common form of arthritis. It is characterized by progressive destruction of articular cartilage and the development of chronic pain and constitutes a considerable socioeconomic burden. Currently, pharmacological treatments mostly aim to relieve the OA symptoms associated with inflammation and pain. However, with increasing understanding of OA pathology, several potential therapeutic targets have been identified, enabling the development of disease-modifying OA drugs (DMOADs). By targeting inflammatory cytokines, matrix-degrading enzymes, the Wnt pathway, and OA-associated pain, DMOADs successfully modulate the degenerative changes in osteoarthritic cartilage. Moreover, regenerative approaches aim to counterbalance the loss of cartilage matrix by stimulating chondrogenesis in endogenous stem cells and matrix anabolism in chondrocytes. Emerging strategies include the development of senolytic drugs or RNA therapeutics to eliminate the cellular or molecular sources of factors driving OA. This review describes the current developmental status of DMOADs and the corresponding results from preclinical and clinical trials and discusses the potential of emerging therapeutic approaches to treat OA.

摘要

骨关节炎(OA)是最常见的关节炎形式。它的特征是关节软骨进行性破坏和慢性疼痛的发展,并构成相当大的社会经济负担。目前,大多数药物治疗主要旨在缓解与炎症和疼痛相关的 OA 症状。然而,随着对 OA 病理学的认识不断加深,已经确定了几个潜在的治疗靶点,从而能够开发出治疗骨关节炎的药物(DMOAD)。通过靶向炎症细胞因子、基质降解酶、Wnt 通路和 OA 相关疼痛,DMOAD 成功地调节了骨关节炎软骨的退行性变化。此外,再生方法旨在通过刺激内源性干细胞中的软骨生成和软骨细胞中的基质合成来抵消软骨基质的损失。新兴策略包括开发选择性细胞凋亡药物或 RNA 治疗药物,以消除导致 OA 的细胞或分子来源。本文描述了 DMOAD 的当前开发状况以及临床前和临床试验的相应结果,并讨论了新兴治疗方法治疗 OA 的潜力。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7915/8640059/1e4a843bdc91/12276_2021_710_Fig1_HTML.jpg

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