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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
来源:
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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