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Updated: Jun 27, 2026

Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
miRNA implication in the pathogenesis and the outcome of Tunisian endemic pemphigus foliaceus
Boudour Khabou1, Raouia Fakhfakh1, Safa Tahri1
1Autoimmunity, Cancer and Immunogenetics Research Laboratory (LR18SP12), Immunology Department, Habib Bourguiba Hospital, University of Sfax, Sfax, Tunisia.
Abstract:
Pemphigus foliaceus (PF) is a bullous autoimmune skin disease diagnosed through sera and skin analyses. PF severity is associated with maintained anti-Dsg1 sera levels and its prognosis is unpredictable. MicroRNA (miRNA), dynamic regulators of immune function, have been identified as potential biomarkers for some autoimmune diseases. This study aimed to assess the miRNA expression of miR-17-5p, miR-21-5p, miR-146a-5p, miR-155-5p and miR-338-3p using quantitative real-time PCR in peripheral blood mononuclear cells (PBMC) and lesional skin samples from untreated and treated PF patients (both remittent and chronic) over 3 months. Overall, miRNA expression was significantly higher in PBMC than in biopsy samples. Blood miR-21 expression was increased in untreated patients compared to controls and had a diagnostic value with an AUC of 0.78. After 6 weeks, it decreased significantly, similar to anti-Dsg1 antibodies and the PDAI score. In addition, a positive correlation was observed between cutaneous miR-21 expression and the disease activity score. Conversely, cutaneous expressions of miR-17, miR-146a and miR-155 were significantly higher in treated chronic patients compared to remittent ones. The cutaneous level of miR-155 positively correlated with pemphigus activity, making it a potential predictive marker for patients' clinical stratification with an AUC of 0.86.These findings suggest that blood miR-21 and cutaneous miR-155 can be used as supplemental markers for PF diagnosis and activity, respectively in addition to classical parameters.
Insights
MicroRNA (miRNA) profiling in pemphigus foliaceus (PF) reveals miR-21 in blood as a diagnostic marker and miR-155 in skin as a predictive marker for disease activity.
Area of Science:
- Immunodermatology
- Molecular Biology
- Biomarker Discovery
Background:
- Pemphigus foliaceus (PF) is an autoimmune blistering skin disease with unpredictable prognosis.
- MicroRNAs (miRNAs) are immune regulators and potential biomarkers for autoimmune conditions.
- Current PF diagnosis relies on sera and skin analyses, with limited prognostic markers.
Purpose of the Study:
- To evaluate specific microRNA (miRNA) expression levels (miR-17-5p, miR-21-5p, miR-146a-5p, miR-155-5p, miR-338-3p) in peripheral blood mononuclear cells (PBMCs) and lesional skin of PF patients.
- To assess the diagnostic and prognostic potential of these miRNAs in relation to disease activity and treatment response.
- To correlate miRNA expression with established PF biomarkers like anti-Dsg1 antibodies and the Pemphigus Disease Area Index (PDAI).
Main Methods:
- Quantitative real-time PCR was used to measure miRNA expression in PBMCs and lesional skin biopsies.
- Samples were collected from untreated, treated remittent, and treated chronic PF patients over a 3-month period.
- Statistical analyses, including Area Under the Curve (AUC) calculations, were performed to determine diagnostic and predictive values.
Main Results:
- Overall miRNA expression was higher in PBMCs than in skin biopsies.
- Blood miR-21 expression was elevated in untreated PF patients (AUC=0.78) and decreased with treatment, correlating with disease activity.
- Cutaneous miR-155 expression was higher in chronic PF patients and positively correlated with disease activity (AUC=0.86), suggesting predictive potential.
Conclusions:
- Blood miR-21 serves as a potential supplemental biomarker for PF diagnosis.
- Cutaneous miR-155 shows promise as a predictive marker for PF activity and clinical stratification.
- These miRNAs offer additional tools alongside traditional parameters for managing PF.
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