Department of Immunology, School of Medicine, Mazandaran University of Medical Sciences, Sari, IRAN; Immunogenetics Research Center, Mazandaran University of Medical Sciences, Sari, Iran.
Anatomical Research Center, Kashan University of Medical Sciences and Health Services, kashan, IRAN.
Cell Immunol. 2024 Nov-Dec;405-406:104876. doi: 10.1016/j.cellimm.2024.104876. Epub 2024 Sep 24.
IBD, an autoimmune-inflammatory disorder that affects people who are genetically prone to inflammation. There is a lot of interest in MSC-CM therapy, especially when primed with TNF-α + IFN-γ. Throughout the study, data were collected on the percentage of apoptotic cells, gene expression of ZO-1, Foxp3, GATA3, IDO-1, Muc2, T-bet, Notch1, TNFR2, and ROR-γt, colon weight and length, histopathological analysis, and DAI. TNF-α and IL-10 levels were assessed in addition to the NO level. The results suggest that primed MSC-CM improved DAI, mucosal deterioration, intestinal inflammation and NO concentration. The amount of TNF-α was decreased, but IL-10 and the colon's percentage of apoptotic cells was increased. The mRNA expression of ZO-1, Foxp3, GATA3, IDO-1, and Muc2 genes increased greatly in the treatment groups, while the expression of T-bet, Notch1, TNFR2, and ROR-γt genes has decreased. These studies suggest that primed MSC-CM may combine with common treatments to improve responsiveness.
IBD,一种自身免疫性炎症性疾病,影响那些易患炎症的遗传倾向人群。MSC-CM 疗法备受关注,特别是在 TNF-α+IFN-γ 预激活后。在整个研究过程中,收集了凋亡细胞的百分比、ZO-1、Foxp3、GATA3、IDO-1、Muc2、T-bet、Notch1、TNFR2 和 ROR-γt 的基因表达、结肠重量和长度、组织病理学分析和 DAI 的数据。除了 NO 水平外,还评估了 TNF-α 和 IL-10 水平。结果表明,预激活的 MSC-CM 改善了 DAI、黏膜恶化、肠道炎症和 NO 浓度。TNF-α 含量减少,但 IL-10 和结肠凋亡细胞的百分比增加。治疗组中 ZO-1、Foxp3、GATA3、IDO-1 和 Muc2 基因的 mRNA 表达大大增加,而 T-bet、Notch1、TNFR2 和 ROR-γt 基因的表达则减少。这些研究表明,预激活的 MSC-CM 可能与常规治疗相结合,以提高反应性。