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滑膜环境可引导软骨的退化和再生。

The synovial environment steers cartilage deterioration and regeneration.

机构信息

Wake Forest Institute for Regenerative Medicine, Wake Forest School of Medicine, Winston Salem, NC, USA.

Skeletal Biology and Research Engineering Center, KU Leuven, Leuven, Belgium.

出版信息

Sci Adv. 2023 Apr 21;9(16):eade4645. doi: 10.1126/sciadv.ade4645.


DOI:10.1126/sciadv.ade4645
PMID:37083524
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10121162/
Abstract

Osteoarthritis (OA) was recently defined as an epidemic, and the lack of effective treatment is highly correlated to the limited knowledge regarding the underlying pathophysiology. Failure to regenerate upon trauma is thought to be one of the underlying causes for degenerative diseases, including OA. To investigate why lesions within an OA environment fail to heal, a heterogeneous cell population was isolated from the synovial fluid (SF) of OA patients. The cells' ability to undergo processes required for functional tissue regeneration was evaluated in the presence or absence of autologous SF. The obtained mechanistic findings were then used for the development of an immunomodulatory cell treatment, aimed to restore the pro-regenerative environment. Intra-articular injection in a clinical compassionate use study showed that the treatment restored the articular cartilage and joint homeostasis of OA patients. These findings confirm the role of pro-regenerative immune cells and their targeted influence on progenitor cells for degenerative joint disease therapies.

摘要

骨关节炎(OA)最近被定义为一种流行病,而缺乏有效治疗方法与对潜在病理生理学知识的有限了解高度相关。人们认为,在创伤后无法再生是包括 OA 在内的退行性疾病的一个潜在原因。为了研究为什么 OA 环境中的病变无法愈合,从 OA 患者的滑膜液 (SF) 中分离出了异质细胞群体。评估了在存在或不存在自体 SF 的情况下,细胞经历功能性组织再生所需过程的能力。然后,将获得的机制研究结果用于开发一种免疫调节细胞治疗方法,旨在恢复具有再生能力的环境。在一项临床同情使用研究中进行的关节内注射表明,该治疗方法恢复了 OA 患者的关节软骨和关节内稳态。这些发现证实了促再生免疫细胞的作用及其对退行性关节疾病治疗中祖细胞的靶向影响。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c26/10121162/263c9c14c25e/sciadv.ade4645-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c26/10121162/19da85efd565/sciadv.ade4645-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c26/10121162/bbcb573d084e/sciadv.ade4645-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c26/10121162/3016df637158/sciadv.ade4645-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c26/10121162/f1195ef285a6/sciadv.ade4645-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c26/10121162/c5a350adcf95/sciadv.ade4645-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c26/10121162/a9a2cdd8411f/sciadv.ade4645-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c26/10121162/263c9c14c25e/sciadv.ade4645-f7.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c26/10121162/19da85efd565/sciadv.ade4645-f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c26/10121162/bbcb573d084e/sciadv.ade4645-f2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c26/10121162/3016df637158/sciadv.ade4645-f3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c26/10121162/f1195ef285a6/sciadv.ade4645-f4.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c26/10121162/c5a350adcf95/sciadv.ade4645-f5.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c26/10121162/a9a2cdd8411f/sciadv.ade4645-f6.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9c26/10121162/263c9c14c25e/sciadv.ade4645-f7.jpg

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本文引用的文献

[1]
Prevalence Trends of Site-Specific Osteoarthritis From 1990 to 2019: Findings From the Global Burden of Disease Study 2019.

Arthritis Rheumatol. 2022-7

[2]
Single-Cell Profiles of Age-Related Osteoarthritis Uncover Underlying Heterogeneity Associated With Disease Progression.

Front Mol Biosci. 2022-1-10

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Front Immunol. 2021

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Immunohorizons. 2021-6-8

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Nature. 2020-11

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Am J Pathol. 2020-6-10

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Adv Wound Care (New Rochelle). 2020-2-7

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Stem Cells Transl Med. 2020-1

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Sci Immunol. 2019-10-11

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Intraarticular injection of processed lipoaspirate cells has anti-inflammatory and analgesic effects but does not improve degenerative changes in murine monoiodoacetate-induced osteoarthritis.

BMC Musculoskelet Disord. 2019-7-19

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