Dynamic expression analysis of peripheral blood derived small extracellular vesicle miRNAs in sepsis progression

Author:

Liu Xinyan1,Yu Dapeng2,Li Tiantian3,Zhu Kehan4,Bi Yang4,Wang Chaofan4,Wang Chunting5,Song Xuan56ORCID

Affiliation:

1. ICU, Dong E Hospital Liaocheng China

2. Cardiac Surgery Department Dong E Hospital Liaocheng China

3. High Dependency Unit Shandong Public Health Clinical Center Jinan China

4. Shandong First Medical University Jinan China

5. ICU, Shandong Provincial Hospital Affiliated to Shandong First Medical University Jinan China

6. Endocrine and Metabolic Diseases Hospital of Shandong First Medical University Jinan China

Abstract

AbstractImmune disorders caused by sepsis have recently drawn much attention. We sought to dynamically monitor the expression of small extracellular vesicle (sEV) miRNAs in peripheral blood during sepsis to explore these miRNAs as potential biomarkers for monitoring immune function in sepsis patients. This study included patients with sepsis. Blood samples were obtained from 10 patients on the first through 10th days, the 12th day and the 14th day since sepsis onset, resulting in 120 collected samples. Serum sEVs were extracted from peripheral venous blood, and levels of MIR497HG, miR‐195, miR‐497, and PD‐L1 in serum sEVs were detected by qPCR, and clinical information was recorded. Our study revealed that the levels of MIR497HG, miR‐195, miR‐497 and PD‐L1 in serum sEVs showed periodic changes; the time from peak to trough was approximately 4–5 days. The levels of sEV MIR497HG and miR‐195 had a positive linear relationship with SOFA score (r values were −0.181 and −0.189; p values were 0.048 and 0.039, respectively). The recorded quantities of sEV MIR497HG, miR‐195 and PD‐L1 showed a substantial correlation with ARDS. ROC curve analysis revealed that sEV MIR497HG, miR‐195 and miR‐497 could predict the 28‐day mortality of sepsis patients with an AUC of 0.66, 0.68 and 0.72, respectively. Levels of sEVs MIR497HG, miR‐195, miR‐497 and PD‐L1 showed periodic changes with the immune status of sepsis, which provides a new exploration direction for immune function biomarkers and immunotherapy timing in sepsis patients.

Funder

National Natural Science Foundation of China

Natural Science Foundation of Shandong Province

Shandong Provincial Postdoctoral Science Foundation

Publisher

Wiley

Subject

Cell Biology,Molecular Medicine

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