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Updated: Mar 8, 2026

Lymphocyte Isolation from Human Skin for Phenotypic Analysis and Ex Vivo Cell Culture
Published on: April 8, 2016
Okt6 Positme Epidermal L4ngerhans Cells in Tinea Corporis
Insights
Tinea corporis lesions show significantly reduced Langerhans cells (LC) compared to normal skin. This decrease in epidermal LC may contribute to the weakened cell-mediated immunity observed in fungal skin infections.
Area of Science:
- Dermatology
- Immunology
- Mycology
Background:
- Tinea corporis is a superficial fungal infection of the skin.
- Langerhans cells (LC) are critical immune cells in the epidermis, playing a role in initiating immune responses.
- The role of LC in the pathogenesis of tinea corporis is not fully understood.
Purpose of the Study:
- To investigate the number and distribution of Langerhans cells in the skin lesions of patients with untreated tinea corporis.
- To assess the potential correlation between LC reduction and cell-mediated immunity (CMI) in this condition.
Main Methods:
- Indirect immunofluorescence was used to identify and quantify Langerhans cells.
- The OKT6 monoclonal antibody was employed to detect LC in skin biopsy specimens.
- Comparison was made between LC in lesional skin and normal skin.
Main Results:
- A significant reduction in the number and distribution of epidermal LC (T6+ cells) was observed in tinea corporis lesions compared to normal skin.
- In most lesions, epidermal LC were undetectable.
- Antigens associated with LC were not found on keratinocytes.
Conclusions:
- The findings suggest a diminished cell-mediated immune response to fungal infection in tinea corporis.
- A reduction in Langerhans cells may be a contributing factor to the altered immune response and pathogenesis of tinea corporis.
Abstract:
Langerhans cells (LC) were defined by indirect immunofluoresence using OKT6 monoclonal antibody in the skin lesions of 11 untreated patients with tinea corporis. The number and distribution of OKr6 + epidermal LC in the lesions was very low in comparison to that found in the normal skin. In most of the lesions, T6 + LC could not be seen in the epidermis. A like antigens were not detectable on the keratinocytes. These observations suggest deceased CMI response to the fungal infection and that the reduction in LC may be a contributing factor in the pathogenesis of tinea corporis.
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