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Effect of Topical Corticosteroid Treatment on microRNA Expression in Infants with Atopic Dermatitis
Janna Nousbeck1, Maeve A McAleer1,2, Elaine M Kenny3
1Clinical Medicine, Trinity College Dublin, Dublin, Ireland.
Abstract:
MicroRNAs (miRNAs) have been implicated in a variety of disorders. Although studies have examined miRNA in pediatric atopic dermatitis (AD), the impact of topical corticosteroid (TCS) therapy on miRNA expression in pediatric AD has not been investigated. We sought to investigate the effects of 6 weeks of TCS therapy on miRNA expression in infants with AD. Small RNA sequencing and real-time RT-qPCR were performed to identify differentially expressed miRNAs in PBMCs of infants with AD after TCS treatment; HTG EdgeSeq was used to identify differentially expressed miRNAs in plasma. Kyoto Encyclopedia of Genes and Genomes pathway enrichment analysis was conducted using a list of experimentally verified miRNA targets sourced from the DIANA-TarBase and miRTarBase databases. Five miRNAs were differentially expressed in circulating PBMCs after TCS treatment (miR-143-3p, miR-27a-5p, miR-126-3p, miR-451a, and miR-223-3p); 12 miRNAs were differentially expressed in plasma. These miRNAs have regulatory functions crucial for regulating cell growth and survival, vascular adhesion, angiogenesis, skin barrier integrity, stress and nervous system processes, immune responses, inflammation, and T helper 17 cell differentiation. TCS treatment led to a distinct miRNA expression profile in peripheral blood, providing insights into how this treatment impacts disease mechanisms in childhood AD.
Insights
Topical corticosteroid (TCS) therapy alters microRNA (miRNA) expression in infants with atopic dermatitis (AD). This study reveals specific miRNA changes in peripheral blood, offering insights into AD treatment mechanisms.
Area of Science:
- Molecular Biology
- Immunology
- Dermatology
Background:
- MicroRNAs (miRNAs) are crucial regulators implicated in various diseases.
- Pediatric atopic dermatitis (AD) involves complex biological pathways.
- The effect of topical corticosteroid (TCS) therapy on miRNA expression in pediatric AD remains uncharacterized.
Purpose of the Study:
- To investigate the impact of 6 weeks of TCS therapy on miRNA expression in infants with AD.
- To identify specific differentially expressed miRNAs in peripheral blood mononuclear cells (PBMCs) and plasma following TCS treatment.
- To understand the functional roles of these miRNAs in AD pathogenesis and treatment response.
Main Methods:
- Small RNA sequencing and real-time RT-qPCR were employed to analyze miRNA expression in PBMCs.
- HTG EdgeSeq technology was utilized for miRNA profiling in plasma.
- Kyoto Encyclopedia of Genes and Genomes (KEGG) pathway enrichment analysis was performed on predicted miRNA targets.
Main Results:
- Five miRNAs (miR-143-3p, miR-27a-5p, miR-126-3p, miR-451a, miR-223-3p) were significantly altered in PBMCs post-TCS treatment.
- Twelve miRNAs exhibited differential expression in plasma after 6 weeks of TCS therapy.
- The identified miRNAs are involved in critical cellular processes including immune response, inflammation, and skin barrier function.
Conclusions:
- TCS treatment induces a distinct miRNA expression signature in the peripheral blood of infants with AD.
- These miRNA alterations provide novel insights into the molecular mechanisms underlying TCS efficacy in pediatric AD.
- Further research into these miRNAs may lead to improved therapeutic strategies for childhood AD.
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