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Updated: Jul 15, 2026

Lymphocyte Isolation from Human Skin for Phenotypic Analysis and Ex Vivo Cell Culture
Published on: April 8, 2016
Leprosy-specific B-cells within cellular infiltrates in active leprosy lesions
Anand M Iyer1, Keshar K Mohanty2, Danielle van Egmond1
1Department of Pathology, Academic Medical Center, Amsterdam 1105AZ, The Netherlands.
Insights
This study reveals B-cells and plasma cells in active leprosy lesions, producing Mycobacterium leprae-specific antibodies. This finding suggests a potential role for B-cells in leprosy immunity and pathology.
Area of Science:
- Immunology
- Dermatology
- Microbiology
Background:
- Leprosy presents a spectrum of forms, from lepromatous to tuberculoid, with varying immune responses.
- While T-cells and macrophages are known infiltrates in leprosy lesions, B-cell presence has been infrequently reported.
Purpose of the Study:
- To investigate the presence and function of B-cells in active leprosy lesions.
- To determine if B-cells contribute to antibody production against Mycobacterium leprae in situ.
Main Methods:
- Immunohistochemical analysis of active leprosy lesions.
- Organotypic skin explant culture model to assess in situ antibody production.
- Cytokine profiling of lesional skin cultures.
Main Results:
- B-cells, including plasma cells, were identified in active lesions across various leprosy forms (lepromatous, borderline lepromatous, borderline tuberculoid).
- In situ production of Mycobacterium leprae-specific antibodies was demonstrated in borderline tuberculoid lesions.
- Lesional skin cultures revealed a cytokine microenvironment supporting B-cell differentiation and maturation.
Conclusions:
- Functionally active B-cells, capable of secreting anti-Mycobacterium leprae antibodies, are present in leprosy lesions, even in borderline tuberculoid forms.
- The specific role of these B-cells in the pathology of leprosy requires further investigation.
Abstract:
Leprosy is a spectral disease with polar lepromatous and tuberculoid forms correlating with enhanced humoral and cell-mediated immunity, respectively, against Mycobacterium leprae and the borderline forms, borderline lepromatous, midborderline, and borderline tuberculoid showing in-between clinical and immunological characteristics. Histopathologically, the cellular infiltrates of leprosy lesions show predominantly the presence of interacting T-cells and antigen presenting cells like macrophages, whereas the presence of B-cells has only been sporadically reported. The present study demonstrates by immunohistochemical techniques the presence of B-cells, including plasma cells, in active lesions from lepromatous leprosy, skin smear negative borderline lepromatous, and paucibacillary borderline tuberculoid leprosy. Furthermore, the study demonstrates the in situ production of M leprae-specific antibodies from BT lesions using an organotypic skin explant culture model. Finally, analysis of the cytokine release profile in supernatants of lesional organotypic skin cultures showed a microenvironment conducive to the differentiation and maturation of B-cells. The results demonstrate the presence of different functionally active B-cell stages within lesions of patients with leprosy, including borderline tuberculoid patients, which could secrete anti-M leprae-specific antibodies. However, their role in leprosy pathology remains to be elucidated.
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