Laboratory of Respiratory Disease, Cell Biology Section, Fondazione IRCCS Policlinico San Matteo, 27100 Pavia, Italy.
Immunohaematology and Transfusion Service, Apheresis and Cell Therapy Unit, Fondazione IRCCS Policlinico San Matteo, 27100 Pavia, Italy.
Cells. 2022 Mar 25;11(7):1117. doi: 10.3390/cells11071117.
Clinical evidence suggests an improvement or stabilization of lung function in a fraction of patients with bronchiolitis obliterans syndrome (BOS) treated by extracorporeal photopheresis (ECP); however, few studies have explored the epigenetic and molecular regulation of this therapy. The aim of present study was to evaluate whether a specific set of miRNAs were significantly regulated by ECP. Total RNA was isolated from serum of patients with established BOS grade 1-2 prior to the start and after 6 months of ECP treatment. We observed a significant downregulation of circulating hsa-miR-155-5p, hsa-miR-146a-5p and hsa-miR-31-5p in BOS patients at the start of ECP when compared to healthy subjects. In responders, increased miR-155-5p and decreased miR-23b-3p expression levels at 6 months were found. SMAD4 mRNA was found to be a common target of these two miRNAs in prediction pathways analysis, and a significant downregulation was found at 6 months in PBMCs of a subgroup of ECP-treated patients. According to previous evidence, the upregulation of miR-155 might be correlated with a pro-tolerogenic modulation of the immune system. Our analysis also suggests that SMAD4 might be a possible target for miR-155-5p. Further longitudinal studies are needed to address the possible role of miR-155 and its downstream targets.
临床证据表明,在接受体外光化学疗法(ECP)治疗的一部分闭塞性细支气管炎综合征(BOS)患者中,肺功能得到改善或稳定;然而,很少有研究探讨这种治疗的表观遗传和分子调节。本研究旨在评估一组特定的 miRNAs 是否被 ECP 显著调节。在开始 ECP 治疗前和 6 个月后,从已确诊为 BOS 1-2 级的患者的血清中分离总 RNA。与健康受试者相比,我们观察到在开始 ECP 时,BOS 患者的循环 hsa-miR-155-5p、hsa-miR-146a-5p 和 hsa-miR-31-5p 显著下调。在反应者中,在 6 个月时发现 miR-155-5p 表达增加和 miR-23b-3p 表达降低。预测途径分析发现 SMAD4 mRNA 是这两个 miRNA 的共同靶标,在 ECP 治疗患者亚组的 PBMC 中,在 6 个月时发现其显著下调。根据先前的证据,miR-155 的上调可能与免疫系统的耐受原性调节有关。我们的分析还表明,SMAD4 可能是 miR-155-5p 的一个可能靶点。需要进一步的纵向研究来探讨 miR-155 及其下游靶标的可能作用。