Chen Yu-Hsiu, Hung Yi-Pei, Chen Chih-Ying, Chen Yi-Ting, Tsai Tai-Chen, Yang Jui-Jung, Wu Chia-Chun
Rheumatology/Immunology and Allergy, Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei 114202, Taiwan.
UnicoCell Biomed Co., Ltd., Taipei 11494, Taiwan.
Curr Issues Mol Biol. 2024 Aug 2;46(8):8395-8406. doi: 10.3390/cimb46080495.
Adipose-derived stem cells (ADSCs) comprise a promising therapy for osteoarthritis (OA). The therapeutic potential of ELIXCYTE, an allogeneic human ADSC (hADSC) product, was demonstrated in a phase I/II OA clinical trial. However, the exact mechanism underlying such effects is not clear. Moreover, studies suggest that interleukin-11 (IL-11) has anti-inflammatory, tissue-regenerative, and immune-regulatory functions. Our aim was to unravel the mechanism associated with the therapeutic effects of ELIXCYTE on OA and its relationship with IL-11. We cocultured ELIXCYTE with normal human articular chondrocytes (NHACs) in synovial fluid obtained from individuals with OA (OA-SF) to investigate its effect on chondrocyte matrix synthesis and degradation and inflammation by assessing gene expression and cytokine levels. NHACs exposed to OA-SF exhibited increased expression. However, coculturing ELIXCYTE with chondrocytes in OA-SF reduced expression in chondrocytes and downregulated and expression in ELIXCYTE. ELIXCYTE treatment elevated anti-inflammatory cytokine (IL-1RA, IL-10, and IL-13) levels, and the reduction in was positively correlated with IL-11 concentrations in OA-SF. These findings indicate that IL-11 in OA-SF might serve as a predictive biomarker for the ELIXCYTE treatment response in OA, emphasizing the therapeutic potential of ELIXCYTE to mitigate OA progression and provide insights into its immunomodulatory effects.
脂肪来源干细胞(ADSCs)为骨关节炎(OA)提供了一种有前景的治疗方法。一种同种异体人ADSC(hADSC)产品ELIXCYTE的治疗潜力在一项I/II期OA临床试验中得到了证实。然而,这种作用的确切机制尚不清楚。此外,研究表明白细胞介素-11(IL-11)具有抗炎、组织再生和免疫调节功能。我们的目的是阐明ELIXCYTE对OA治疗作用的相关机制及其与IL-11的关系。我们将ELIXCYTE与从OA患者(OA-SF)获得的滑液中的正常人关节软骨细胞(NHACs)共培养,通过评估基因表达和细胞因子水平来研究其对软骨细胞基质合成、降解和炎症的影响。暴露于OA-SF的NHACs表达增加。然而,在OA-SF中将ELIXCYTE与软骨细胞共培养可降低软骨细胞中的表达,并下调ELIXCYTE中的和表达。ELIXCYTE治疗可提高抗炎细胞因子(IL-1RA、IL-10和IL-13)水平,且的降低与OA-SF中IL-11浓度呈正相关。这些发现表明,OA-SF中的IL-11可能作为OA中ELIXCYTE治疗反应的预测生物标志物,强调了ELIXCYTE减轻OA进展的治疗潜力,并为其免疫调节作用提供了见解。