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Updated: Aug 8, 2026

Lymphocyte Isolation from Human Skin for Phenotypic Analysis and Ex Vivo Cell Culture
Published on: April 8, 2016
Recent physiopathological insights in cutaneous lymphocytic infiltrates
1Institut de Recherche sur la Peau et Service de Dermatologie, Hôpital Saint-Louis, 1, avenue Claude-Vellefaux, 75475 Paris Cedex 10, France. h-bachelez@chu-stlouis.fr
Insights
Benign cutaneous lymphocytic infiltrates (CLI) are classified by clinicopathology and T-cell phenotype. Recent studies reveal clonal expansions and antigen-driven mechanisms in HIV-associated pseudolymphomas, improving CLI understanding.
Area of Science:
- Dermatology
- Immunology
- Pathology
Background:
- Benign cutaneous lymphocytic infiltrates (CLI) encompass diverse entities.
- Classification relies on clinicopathological findings and lymphocytic subset phenotypes.
- Recent focus on clonality status using PCR amplification of TCR/Ig loci.
Purpose of the Study:
- To characterize clonal benign cutaneous lymphocytic expansions.
- To investigate oligoclonal patterns in HIV-associated CD8 cutaneous pseudolymphomas.
- To understand the role of antigen-driven mechanisms in pseudolymphoma pathogenesis.
Main Methods:
- Highly sensitive assays utilizing PCR amplification of TCR/Ig loci.
- Phenotypic analysis of lymphocytic subsets within skin infiltrates.
- Functional studies of skin-infiltrating lymphocytes.
Main Results:
- Characterization of clonal benign cutaneous lymphocytic expansions.
- Evidence of oligoclonal patterns in HIV-associated CD8 cutaneous pseudolymphomas.
- Identification of antigen-driven mechanisms in pseudolymphoma pathogenesis.
Conclusions:
- Clonality assessment enhances understanding of benign CLI.
- Antigen-driven mechanisms are implicated in HIV-associated pseudolymphomas.
- Cutaneous Lymphocyte-associated Antigen (CLA) aids in identifying skin-homing T cells.
Abstract:
The spectrum of benign cutaneous lymphocytic infiltrates (CLI) includes a variety of entities which are classified on the basis of clinicopathological findings, and of the phenotype of the predominant lymphocytic subset among the skin infiltrate. Major concern has been recelntly given to the clonality status of CLI by using highly sensitive assays based on the PCR amplification of TCR/Ig loci. These studies allowed the characterisation of clonal benighn cutaneous lymphocytic expansions. Other studies have shown evidence of oligoclonal patterns in HIV-associated CD8 cutaneous pseudolymphomas, and functionnal studies of the skin infiltrate further showed that an antigen-driven mechanism was involved in the pathogenesis of this latter entity. Finally, the knowledge in the field of CLI has been improved by the identification of antigens associated with skin-homing properties such as the so-called. Cutaneous Lymphocyte-associated Antigen (CLA) whicis expressed at the surface of most memory T cells infiltrating the dermis in inflammatory conditions.
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