Mechanisms of Action of Extracorporeal Photopheresis in the Control of Bronchiolitis Obliterans Syndrome (BOS): Involvement of Circulating miRNAs

被引:7
|
作者
Bozzini, Sara [1 ]
Del Fante, Claudia [2 ]
Morosini, Monica [1 ]
Berezhinskiy, Hatice Oya [3 ]
Auner, Sophia [3 ]
Cattaneo, Elena [1 ]
Della Zoppa, Matteo [1 ]
Pandolfi, Laura [1 ]
Cacciatore, Rosalia [2 ]
Perotti, Cesare [2 ]
Hoetzenecker, Konrad [3 ]
Jaksch, Peter [3 ]
Benazzo, Alberto [3 ]
Meloni, Federica [4 ]
机构
[1] Fdn IRCCS Policlin San Matteo, Cell Biol Sect, Lab Resp Dis, I-27100 Pavia, Italy
[2] Fdn IRCCS Policlin San Matteo, Immunohaematol & Transfus Serv, Apheresis & Cell Therapy Unit, I-27100 Pavia, Italy
[3] Med Univ Vienna, Dept Thorac Surg, A-1090 Vienna, Austria
[4] Fdn IRCCS Policlin San Matteo, UOS Transplant Ctr, I-27100 Pavia, Italy
关键词
circulating microRNAs; BOS; ECP; VERSUS-HOST-DISEASE; REGULATORY T-CELLS; LUNG-TRANSPLANT; DENDRITIC CELLS; IN-VITRO; MICRORNAS; INDUCTION; PHOTOCHEMOTHERAPY; INFLAMMATION; EFFICACY;
D O I
10.3390/cells11071117
中图分类号
Q2 [细胞生物学];
学科分类号
071009 ; 090102 ;
摘要
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.
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页数:14
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