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Colloid body formation in bullous pemphigoid
Archives of Dermatological Research
|January 1, 1985
Summary
Researchers identified unique fibrillar bodies in bullous pemphigoid (BP) skin biopsies. These bodies, formed from degenerated keratinocytes, resemble colloid bodies seen in other skin diseases.
Area of Science:
- Dermatology
- Immunopathology
- Cell Biology
Background:
- Bullous pemphigoid (BP) is an autoimmune blistering disease.
- Characteristic immune deposits are found at the basement membrane zone in BP.
- The origin and nature of certain histological findings in BP require further elucidation.
Purpose of the Study:
- To characterize the nature of homogeneous and globular fluorescent bodies observed in bullous pemphigoid skin biopsies.
- To investigate the potential origin of these bodies from degenerated keratinocytes.
- To compare these findings with colloid bodies in other dermatoses.
Main Methods:
- Direct immunofluorescence (IF) using FITC-labelled antisera.
- Immunoperoxidase staining.
- Haematoxylin/eosin (HE) and Periodic Acid-Schiff (PAS) staining.
- Electron microscopy.
Main Results:
- Immunoglobulin and complement deposits were observed at the basement-membrane zone (BMZ).
- Homogeneous and globular fluorescent bodies were detected in the uppermost dermis and/or blisters in a subset of BP specimens.
- These bodies were PAS positive, slightly eosinophilic, and composed of microfilaments (7-8 nm diameter) under electron microscopy.
- Histological, immunohistological, and ultrastructural features were consistent with colloid bodies.
Conclusions:
- Degenerated keratinocytes in the blister roof may transform into these fibrillar bodies.
- These bodies are histologically similar to colloid bodies found in other inflammatory skin conditions.
- The findings provide insights into the cellular changes and potential pathogenetic mechanisms in bullous pemphigoid.