Differential expression of exosomal miRNAs and proteins in the plasma of systemic lupus erythematous patients

Systemic lupus erythematous (SLE) is a complex chronic autoimmune disease with difficult early treatment and accurate diagnosis. Circulating exosomes containing proteins, lipids and nucleic acids can be ideal diagnostic biomarkers and disease management strategies for SLE. Our aim was to examine the unique expression profiles of circulating exosomal miRNAs and proteins in patients with SLE patients. Using RNA-sequencing and proteomic approaches, we compared the expression patterns of exosomal miRNAs and proteins in the plasma of SLE patients and healthy subjects, and discussed the underlying signaling network of circulating exosomes. We also summarize common molecules (miRNAs and proteins) and pathways shared by our plasma exosomes, as well as previously reported data (PBMC, T cells, B cells and plasma). We identified groups of differentially expressed exosomal miRNAs and proteins in the plasma of SLE patients and healthy controls. We obtained consensus molecules (39 miRNAs, 14 proteins) and 21 signaling pathways that are common in our current study and previous reports. Common molecules (miRNAs and proteins) and pathways shared by our plasma exosomes data and other circulating components data reported previously indicate their potential application in the clinical treatment and diagnosis of SLE disease.

Automated summary

This study examined the expression profiles of exosomal miRNAs and proteins in the plasma of SLE patients and healthy subjects and discussed the underlying signaling network of circulating exosomes. The study identified differentially expressed exosomal miRNAs and proteins in SLE patients and healthy controls, as well as consensus molecules and signaling pathways. These findings indicate the potential application of exosomes in the clinical treatment and diagnosis of SLE disease.