• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

了解骨关节炎的炎症方面:来自免疫检查点抑制剂的经验教训。

Understanding the Inflammatory Aspect of Osteoarthritis: Lessons from Immune Checkpoint Inhibitors.

作者信息

Portnoy Daniel M, Paiola Matthieu, Tymm Carly, Winchester Robert, Mor Adam, Gartshteyn Yevgeniya

机构信息

Division of Rheumatology, Department of Medicine, Columbia University Irving Medical Center, New York, NY 10032, USA.

Herbert Irving Comprehensive Cancer Center, Columbia University Irving Medical Center, New York, NY 10032, USA.

出版信息

J Clin Med. 2026 Jan 14;15(2):658. doi: 10.3390/jcm15020658.

DOI:10.3390/jcm15020658
PMID:41598595
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12841676/
Abstract

Osteoarthritis (OA) is the most prevalent form of arthritis and is a major global health burden. OA is a heterogeneous condition with multiple contributing mechanisms that characterize different subtypes and stages of the disease. In this review, we examine the insights gained into the immunological characteristics of OA that have emerged from the increasingly widespread use of checkpoint inhibitors in the immunotherapy of malignancies. We discuss how the conventional view of OA as a degenerative disease is changing in view of the evidence suggesting that OA has an inflammatory component along with the presence in joint tissue of peripherally tolerized autoreactive resident memory T cells, which upon release of their inhibition by immunotherapy mediate immune-related adverse event arthritis (irAE-arthritis). We review clinical trials evaluating the efficacy of immunosuppressive therapies in modifying the course of OA, thereby providing an additional perspective on the presence and nature of the inflammation in OA. In summary, we argue that a shift from the traditional understanding of OA as a mechanical disease to one that incorporates the role of synovial immune cells and mechanisms of self-tolerance is necessary to guide future therapies, including the use of immune checkpoints for patients with OA.

摘要

骨关节炎(OA)是最常见的关节炎形式,也是一项重大的全球健康负担。OA是一种异质性疾病,具有多种促成机制,这些机制表征了该疾病的不同亚型和阶段。在本综述中,我们考察了随着检查点抑制剂在恶性肿瘤免疫治疗中的使用日益广泛,人们对OA免疫特征所获得的见解。我们讨论了鉴于有证据表明OA具有炎症成分,且关节组织中存在外周耐受的自身反应性驻留记忆T细胞,而传统上将OA视为退行性疾病的观点是如何发生变化的,这些T细胞在免疫治疗解除其抑制后会介导免疫相关不良事件性关节炎(irAE-关节炎)。我们回顾了评估免疫抑制疗法改变OA病程疗效的临床试验,从而为OA炎症的存在和性质提供了另一个视角。总之,我们认为有必要从传统上将OA理解为机械性疾病,转变为纳入滑膜免疫细胞作用和自身耐受机制的理解,以指导未来的治疗,包括对OA患者使用免疫检查点。

相似文献

1
Understanding the Inflammatory Aspect of Osteoarthritis: Lessons from Immune Checkpoint Inhibitors.了解骨关节炎的炎症方面:来自免疫检查点抑制剂的经验教训。
J Clin Med. 2026 Jan 14;15(2):658. doi: 10.3390/jcm15020658.
2
Osteoarthritis increases the risk of inflammatory arthritis due to immune checkpoint inhibitors associated with tissue-resident memory T cells.骨关节炎会增加因与组织驻留记忆T细胞相关的免疫检查点抑制剂导致的炎性关节炎风险。
J Immunother Cancer. 2025 Mar 21;13(3):e010758. doi: 10.1136/jitc-2024-010758.
3
Adaptive immunity in osteoarthritis: Mechanisms and opportunities for regulatory T-cell-targeted therapy.
Pharmacol Res. 2025 Dec;222:108041. doi: 10.1016/j.phrs.2025.108041. Epub 2025 Nov 19.
4
Intra-articular viscosupplementation with hylan g-f 20 to treat osteoarthritis of the knee: an evidence-based analysis.使用透明质酸钠凝胶20进行膝关节腔内粘弹性补充治疗骨关节炎:一项循证分析。
Ont Health Technol Assess Ser. 2005;5(10):1-66. Epub 2005 Jun 1.
5
The association of osteoarthritis with the risk of de novo inflammatory arthritis in patients receiving immune checkpoint inhibitors: a retrospective study.
medRxiv. 2026 Jan 30:2026.01.28.26344880. doi: 10.64898/2026.01.28.26344880.
6
Breaking the cycle: How immune reprogramming and modulation are redefining Osteoarthritis care.
Eur J Pharmacol. 2026 Jan 20;1012:178494. doi: 10.1016/j.ejphar.2025.178494. Epub 2025 Dec 18.
7
Immune cells differentiation in osteoarthritic cartilage damage: friends or foes?骨关节炎软骨损伤中免疫细胞的分化:朋友还是敌人?
Front Immunol. 2025 Mar 25;16:1545284. doi: 10.3389/fimmu.2025.1545284. eCollection 2025.
8
Role of inflammation in the pathogenesis of osteoarthritis: latest findings and interpretations.炎症在骨关节炎发病机制中的作用:最新发现与诠释。
Ther Adv Musculoskelet Dis. 2013 Apr;5(2):77-94. doi: 10.1177/1759720X12467868.
9
The Role of Adipokines between Genders in the Pathogenesis of Osteoarthritis.性激素在骨关节炎发病机制中的作用。
Int J Mol Sci. 2024 Oct 9;25(19):10865. doi: 10.3390/ijms251910865.
10
The Role of Innate Immunity in Osteoarthritis and the Connotation of "Immune-joint" Axis: A Narrative Review.先天性免疫在骨关节炎中的作用及“免疫-关节”轴的内涵:一篇叙述性综述
Comb Chem High Throughput Screen. 2024;27(15):2170-2179. doi: 10.2174/0113862073264389231101190637.

本文引用的文献

1
Safety and effectiveness of immune checkpoint inhibitors in patients with preexisting autoimmune diseases: a systematic review.
Front Immunol. 2025 Nov 18;16:1712632. doi: 10.3389/fimmu.2025.1712632. eCollection 2025.
2
Inhibitory PD-1 axis maintains high-avidity stem-like CD8 T cells.抑制性PD-1轴维持高亲和力的干细胞样CD8 T细胞。
Nature. 2026 Jan;649(8095):194-204. doi: 10.1038/s41586-025-09440-x. Epub 2025 Nov 26.
3
Lineage plasticity and signal dysregulation define the cellular trajectory of osteoarthritis progression.谱系可塑性和信号失调决定了骨关节炎进展的细胞轨迹。
Clin Exp Med. 2025 Nov 25;26(1):41. doi: 10.1007/s10238-025-01947-x.
4
Single-cell sequencing reveals a senescent immune landscape in bone marrow lesions inducing articular cartilage damage in osteoarthritis.
Bone Res. 2025 Nov 21;13(1):94. doi: 10.1038/s41413-025-00467-4.
5
Single-cell sequencing reveals the immune microenvironment in osteoarthritis: from heterogeneity to therapeutic targets.
Int Immunopharmacol. 2025 Nov 14;165:115521. doi: 10.1016/j.intimp.2025.115521. Epub 2025 Sep 10.
6
Cellular and molecular mechanisms underlying subchondral bone remodeling and associated pain in osteoarthritis.骨关节炎中软骨下骨重塑及相关疼痛的细胞和分子机制
Connect Tissue Res. 2025 Aug 13:1-7. doi: 10.1080/03008207.2025.2540950.
7
PD-1 is requisite for skin T cell formation and specification by TGFβ.程序性死亡受体1(PD-1)是转化生长因子β(TGFβ)形成和分化皮肤T细胞所必需的。
Nat Immunol. 2025 Aug;26(8):1339-1351. doi: 10.1038/s41590-025-02228-1. Epub 2025 Jul 29.
8
Tissue-resident memory CD4 T cells infiltrate the CNS in progressive multiple sclerosis and contribute to chronic autoimmunity in mice.组织驻留记忆性CD4 T细胞在进展性多发性硬化症中浸润中枢神经系统,并在小鼠中导致慢性自身免疫。
Sci Transl Med. 2025 Jul 23;17(808):eadp8109. doi: 10.1126/scitranslmed.adp8109.
9
Glucagon-Like Peptide-1 (GLP-1) receptor agonists in rheumatology: A review of current evidence and future directions.胰高血糖素样肽-1(GLP-1)受体激动剂在风湿病学中的应用:当前证据与未来方向综述
Autoimmun Rev. 2025 Aug 29;24(9):103864. doi: 10.1016/j.autrev.2025.103864. Epub 2025 Jul 3.
10
Low-Dose Methotrexate for the Treatment of Inflammatory Knee Osteoarthritis: A Randomized Clinical Trial.小剂量甲氨蝶呤治疗炎性膝关节骨关节炎:一项随机临床试验
JAMA Intern Med. 2025 Jun 2. doi: 10.1001/jamainternmed.2025.1359.