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Updated: Jun 22, 2026

Granulocyte-dependent Autoantibody-induced Skin Blistering
Published on: October 12, 2012
The final destiny of acantholytic cells in pemphigus is Fas mediated
M G Pacheco-Tovar1, E Avalos-Díaz, E Vega-Memije
1Department of Immunology, Unidad Académica de Biología Experimental, Universidad Autónoma de Zacatecas, Guadalupe, Zacatecas, México.
Background:
Pemphigus is an autoimmune disease characterized by the formation of intra-epidermal blisters. Patients develop auto-antibodies against desmoglein 1 and 3 proteins and induce acantholysis.
Objective:
This work addresses the issue of whether the Fas pathway mediates acantholysis. Furthermore, the possible suppliers of the Fas pathway were investigated.
Methods:
Seventeen biopsies of pemphigus patients were studied by haematoxylin and eosin staining, and apoptosis was defined by TUNEL. The expression of Fas, FasL and caspase 3 was studied by in situ hybridization and immunohistochemistry. Cell infiltrates were studied by immunofluorescence with monoclonal anti-CD3, CD4, CD8, CD19 and CD69.
Results:
All of the biopsies showed intra-epidermal blisters, acantholytic cells and inflammatory infiltrates. The blisters expressed Fas, FasL and caspase 3. Cell infiltrates were composed of CD8 and a few CD4(+)CD69(+) cells. Additionally, CD19(+) cells were detected. Interestingly, the Fas expression was increased in acantholytic cells and perilesional keratinocytes. Incidentally, these cells exhibited apoptotic features. Interestingly, the CD8 cells expressed FasL.
Conclusion:
This paper presents the morphological evidence that apoptosis and acantholysis are linked. Therefore, the Fas pathway is associated with CD8 cells in pemphigus lesions.
Insights
In pemphigus, apoptosis and acantholysis are linked via the Fas pathway. CD8 cells are associated with this pathway in pemphigus lesions, suggesting a role in disease pathogenesis.
Area of Science:
- Dermatology
- Immunology
- Cell Biology
Background:
- Pemphigus is an autoimmune blistering disease.
- Autoantibodies target desmoglein 1 and 3, causing acantholysis.
- The role of the Fas pathway in pemphigus acantholysis is unclear.
Purpose of the Study:
- Investigate Fas pathway involvement in pemphigus acantholysis.
- Identify cellular sources of Fas pathway components in pemphigus lesions.
Main Methods:
- Analysis of 17 pemphigus patient biopsies.
- Histopathology (H&E), apoptosis (TUNEL), and immunohistochemistry (Fas, FasL, caspase 3).
- Immunofluorescence for cell infiltrates (CD3, CD4, CD8, CD19, CD69).
Main Results:
- Biopsies showed intra-epidermal blisters, acantholysis, and inflammatory infiltrates.
- Fas, FasL, and caspase 3 were expressed in blisters.
- Increased Fas expression and apoptotic features were observed in acantholytic cells and keratinocytes; CD8 cells expressed FasL.
Conclusions:
- Morphological evidence links apoptosis and acantholysis in pemphigus.
- The Fas pathway is implicated in pemphigus pathogenesis.
- CD8 cells are associated with the Fas pathway in pemphigus lesions.
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