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Skin Biopsy for Diagnosing Discoid Lupus Erythematosus
Published on: June 10, 2025
IL-17 in cutaneous lupus erythematosus.
C Tanasescu1, E Balanescu, P Balanescu
1Colentina Clinical Hospital, Bucharest, Romania. coman.tanasescu@gmail.com
European Journal of Internal Medicine
|May 25, 2010
Summary
Interleukin-17 (IL-17) isoforms IL-17A and IL-17F are elevated in the skin and serum of patients with lupus erythematosus (LE), suggesting their role in disease pathogenesis. This study investigated IL-17 expression in various lupus subtypes.
Area of Science:
- Immunology
- Dermatology
- Rheumatology
Background:
- Lupus erythematosus (LE) is a complex autoimmune disease with diverse clinical manifestations.
- The role of Interleukin-17 (IL-17) isoforms, specifically IL-17A and IL-17F, in the pathogenesis of LE remains incompletely understood.
- This research investigates the local and systemic expression of IL-17 in different forms of lupus skin disease.
Purpose of the Study:
- To evaluate the expression of IL-17A and IL-17F in the skin and serum of patients with discoid lupus erythematosus (DLE), systemic lupus erythematosus (SLE), and subacute cutaneous lupus erythematosus (SCLE).
- To correlate local and serological IL-17 levels with disease activity and specific autoantibodies.
- To elucidate the involvement of IL-17 isoforms in the immunopathogenesis of various lupus erythematosus subtypes.
Main Methods:
- Recruitment of 89 subjects, including patients with psoriasis, healthy controls, DLE, SLE, and SCLE.
- Collection of blood samples and skin biopsy specimens for analysis.
- Quantification of serum IL-17A, IL-17F, and IL-23 using ELISA, and assessment of skin IL-17A and CD4 expression via immunohistochemistry.
Main Results:
- Immunohistochemical analysis revealed significantly higher IL-17A expression in the skin of DLE, SCLE, and SLE patients compared to controls.
- Serum IL-17A levels were elevated in DLE and SLE patients but not in SCLE patients relative to controls.
- Serum IL-17F concentrations were significantly higher across all lupus patient groups (DLE, SCLE, SLE) compared to healthy controls, while IL-23 levels were comparable across groups.
Conclusions:
- IL-17 isoforms, IL-17A and IL-17F, are implicated in the immunopathogenesis of systemic lupus erythematosus (SLE).
- These IL-17 isoforms also play a significant role in the development of discoid lupus erythematosus (DLE) and subacute cutaneous lupus erythematosus (SCLE).
- The findings highlight IL-17 as a potential therapeutic target in various forms of lupus erythematosus.
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