Cheng Xiaohui, Shao Pingwen, Wang XinTong, Jiang Juan, Chen Jiahui, Zhu Jie, Zhu Weiming, Li Yi, Zhang Junfeng, Chen Jiangning, Huang Zhen
State Key Laboratory of Pharmaceutical Biotechnology, School of Life Sciences, Nanjing University, Nanjing, Jiangsu, 210023, China.
Department of General Surgery, Jinling Hospital, School of Medicine, Nanjing University, Nanjing, Jiangsu, 210002, China.
Adv Sci (Weinh). 2025 Feb;12(8):e2411711. doi: 10.1002/advs.202411711. Epub 2024 Dec 31.
Intestinal fibrosis, a severe complication of Crohn's disease (CD), is linked to chronic inflammation, but the precise mechanism by which immune-driven intestinal inflammation leads to fibrosis development is not fully understood. This study investigates the role of myeloid-derived suppressor cells (MDSCs) in intestinal fibrosis in CD patients and a 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced mouse model. Elevated MDSCs are observed in inflamed intestinal tissues prior to fibrosis and their sustained presence in fibrotic tissues of both CD patients and murine models. Depletion of MDSCs significantly reduces fibrosis, highlighting their key role in the fibrotic process. Mechanistically, MDSC-derived mCCL6 activates fibroblasts via the CCR1-MAPK signaling, and interventions targeting this axis, including neutralizing antibodies, a CCR1 antagonist, or fibroblast-specific Ccr1 knockout mice reduce fibrosis. In CD patients with stenosis, human CCL15, analogous to mCCL6, is found to be elevated in MDSCs and activated fibroblasts. Additionally, CXCR2 and CCR2 ligands are identified as key mediators of MDSC recruitment in intestinal fibrosis. Blocking MDSC recruitment with CXCR2 and CCR2 antagonists alleviates intestinal fibrosis. These findings suggest that strategies targeting MDSC recruitment and mCCL6/hCCL15 signaling could offer therapeutic benefits for intestinal fibrosis.
肠道纤维化是克罗恩病(CD)的一种严重并发症,与慢性炎症相关,但免疫驱动的肠道炎症导致纤维化发展的确切机制尚未完全明确。本研究调查了髓系来源抑制细胞(MDSCs)在CD患者肠道纤维化以及三硝基苯磺酸(TNBS)诱导的小鼠模型中的作用。在纤维化之前,在发炎的肠道组织中观察到MDSCs升高,并且它们持续存在于CD患者和小鼠模型的纤维化组织中。MDSCs的消耗显著减少纤维化,突出了它们在纤维化过程中的关键作用。从机制上讲,MDSC衍生的mCCL6通过CCR1-MAPK信号激活成纤维细胞,针对该轴的干预措施,包括中和抗体、CCR1拮抗剂或成纤维细胞特异性Ccr1基因敲除小鼠,可减少纤维化。在患有狭窄的CD患者中,发现与mCCL6类似的人CCL15在MDSCs和活化的成纤维细胞中升高。此外,CXCR2和CCR2配体被确定为肠道纤维化中MDSC募集的关键介质。用CXCR2和CCR2拮抗剂阻断MDSC募集可减轻肠道纤维化。这些发现表明,针对MDSC募集和mCCL6/hCCL15信号的策略可能为肠道纤维化提供治疗益处。