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Published on: August 11, 2018
Acne inversa: evaluating antimicrobial peptides and proteins.
Falk G Bechara1, Michael Sand, Marina Skrygan
1Department of Dermatology, Venerology and Allergology, Ruhr-University Bochum, Bochum, Germany.
The innate immune system plays a key role in acne inversa. Antimicrobial peptides (AMPs) like human β-defensin-2 (hBD-2) and LL-37 are significantly upregulated in acne inversa lesions, indicating their involvement in this inflammatory skin disease.
Area of Science:
- Dermatology
- Immunology
- Molecular Biology
Background:
- Acne inversa is a chronic, inflammatory skin condition affecting specific body areas.
- The innate immune system is implicated in the development of acne inversa.
Purpose of the Study:
- To investigate the role of the innate immune system in acne inversa pathogenesis.
- To compare immune markers in acne inversa lesions with non-lesional skin and chronic venous leg ulcers.
Main Methods:
- Skin biopsies from acne inversa patients (lesional and non-lesional) and controls with chronic venous leg ulcers.
- Quantitative real-time PCR to measure mRNA levels of antimicrobial peptides (AMPs) and cytokines.
- Analysis included human β-defensin (hBD)-1, hBD-2, hBD-3, LL-37, Ribonuclease 7 (RNase 7), TNF-α, MMP1, IL-1β, IL-6, IL-8, and IL-10.
Main Results:
- Acne inversa lesions showed significantly higher mRNA levels of hBD-2, LL-37, IL-1β, IL-6, IL-8, IL-10, and MMP1 compared to non-lesional skin.
- Positive correlations were found between hBD-2 and LL-37, and between hBD-2 and RNase 7 mRNA expression.
- Acne inversa lesions had higher RNase 7 mRNA than leg ulcers, while leg ulcers showed higher expression of IL-1β, IL-6, IL-8, TNF-α, and MMP1.
Conclusions:
- The profile of AMPs, cytokines, and proteases in acne inversa lesions differs from normal skin and leg ulcers.
- Upregulation of AMPs in acne inversa suggests a significant role for the innate immune system in its pathogenesis.
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