Serum miRNAs as potential biomarkers for the bronchiolitis obliterans syndrome after lung transplantation

被引:19
作者
Budding, K. [1 ]
Rossato, M. [1 ,2 ]
van de Graaf, E. A. [3 ]
Kwakkel-van Erp, J. M. [3 ]
Radstake, T. R. D. J. [1 ,2 ]
Otten, H. G. [1 ]
机构
[1] Univ Med Ctr Utrecht, Lab Translat Immunol, F-03-821,POB 85500, NL-3508 GA Utrecht, Netherlands
[2] Univ Med Ctr Utrecht, Dept Rheumatol & Clin Immunol, Utrecht, Netherlands
[3] Univ Med Ctr Utrecht, Dept Resp Med, Utrecht, Netherlands
关键词
Lung transplantation; Chronic lung allograft dysfunction; Bronchiolitis obliterans syndrome; Micro-RNAs; Biomarker; MICRORNAS; EXPRESSION;
D O I
10.1016/j.trim.2017.04.002
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Lung transplantation (LTx) is the last treatment for patients suffering from end-stage lung diseases. Survival post-LTx is hampered by the development of the bronchiolitis obliterans syndrome (BOS) and diagnosis is often late. Given the urgent clinical need to recognize BOS patients at an early stage, we analyzed circulating miRNAs to identify possible stratification markers for BOS development post-transplantation. Therefore, pro-fibrotic (miR-21, miR-155), anti-fibrotic (miR-29a) and fibrosis-unrelated (miR-103, miR-191) miRNAs were analyzed in serum of end-stage lung disease patients and during LTx follow-up. Significant elevated levels of serum miRNAs were observed for all investigated miRNAs in both chronic obstructive pulmonary disease and interstitial lung disease patients compared to healthy controls. The same miRNAs were also significantly increased in the serum of BOS + vs. BOS - patients. Most importantly, miR-21, miR-29a, miR-103, and miR-191 levels were significantly higher in BOS + patients prior to clinical BOS diagnosis. We demonstrated that a selected group of miRNAs investigated is elevated in end-stage lung disease and BOS + patients, prior to clinical BOS diagnosis. Even if further research is expedient on the prognostic value of circulating miRNAs in BOS and lung conditions in general, these results strongly suggest that circulating miRNAs could be used as potential biomarkers for BOS development.
引用
收藏
页码:1 / 4
页数:4
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