Volume 110, Issue 7 pp. 2221-2229
REGULAR ARTICLE

MicroRNA profiling in Chinese children with Henoch-Schonlein purpura and association between selected microRNAs and inflammatory biomarkers

Jing Li

Corresponding Author

Jing Li

Department of Pediatrics, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China

Correspondence

Jing Li, Department of Pediatrics, The First Affiliated Hospital of Jinzhou Medical University, No. 2, Section 5, Renmin Street, Jinzhou 121000, Liaoning, China.

Email: [email protected]

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Meixue Chen

Meixue Chen

Department of Pediatrics, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China

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Jinfeng Wang

Jinfeng Wang

Department of Pediatrics, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China

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Lingling Lu

Lingling Lu

Department of Pediatrics, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China

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Xiang Li

Xiang Li

Department of Pediatrics, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China

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Yuan Le

Yuan Le

Department of Pediatrics, The First Affiliated Hospital of Jinzhou Medical University, Jinzhou, China

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First published: 03 February 2021
Citations: 6

Abstract

Aim

This study aimed to profile the microRNA levels in Chinese Henoch-Schonlein purpura (HSP) children and to explore their association with inflammatory factors and T helper 17 (Th17)/regulatory T (Treg).

Methods

Forty-five HSP children and 27 healthy controls were enrolled in this study, and microRNA levels were profiled with a microRNA microarray. The levels of selected microRNAs were determined by quantitative real-time PCR, and the levels of serum IgA, interleukin-6, interleukin-10 and interleukin-17A were detected by enzyme-linked immunosorbent assay. Additionally, Th17 and Treg cells were analysed by flow cytometry.

Results

There were 9 up-regulated and 27 down-regulated microRNAs in the PBMCs of Chinese HSP children. Among them, miR-1-3p, miR-19b-1-5p and miR-29b-1-5p were up-regulated, while miR-483-5p and miR-1246 were down-regulated. Additionally, these selected microRNAs could differentiate HSP patients from healthy controls. Interestingly, miR-29b-1-5p was correlated with IgA, miR-19b-1-5p, miR-483-5p and miR-1246 were correlated with interleukin-6, while miR-1-3p and miR-1246 were correlated with Th17/Treg.

Conclusion

This study reveals that the altered microRNAs could differentiate HSP from the healthy, and were associated with inflammatory factors or Th17/Treg. It is indicated that alteration in these microRNAs may contribute to the HSP pathogenesis and may become therapeutic targets or diagnostic biomarkers for HSP.

CONFLICT OF INTEREST

The authors have no conflicts of interest to declare.

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