Immunohistological analysis of the lymphoid infiltrate in cutaneous malignant melanomas |
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Authors: | Elisabeth Ralfkiaer Klaus Hou-Jensen Kevin C. Gatter Krzysztof T. Drzewiecki David Y. Mason |
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Affiliation: | (1) Department of Pathology, the Finsen Institute, University of Copenhagen, Strandboulevarden 49, DK-2100 Copenhagen, Denmark;(2) Nuffield Department of Pathology, John Radcliffe Hospital, University of Oxford, England;(3) Department of Plastic Surgery, the Finsen Institute, University of Copenhagen, Denmark |
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Abstract: | Summary The immunological phenotypes of the lymphoid cells in 39 cutaneous malignant melanomas have been investigated by staining cryostat sections with a panel of 20 monoclonal antibodies against lymphoid cells and their subsets. Staining was performed by the alkaline phosphatase: anti-alkaline phosphatase (APAAP) method in which the substrate label (red) is easily distinguishable from melanin. The lymphoid infiltrates had an essentially identical composition in all cases, consisting of T-lymphocytes associated with both Langerhans cells and HLA-DR-positive tissue macrophages. B-lymphocytes and natural killer cells were either absent or only present in low numbers. The ratio between T8 (suppressor/cytotoxic) and T4 (helper/inducer) lymphocytes varied and showed no correlation with melanoma subtype, level of invasion or magnitude of lymphocytic response. Examination for markers associated with T-cell activation and/or with cell proliferation revealed that all lesions contained HLA-DR-positive T-lymphocytes, whereas expression of the transferrin receptor and the interleukin-2 receptor (Tac-antigen) occurred mainly in melanomas with a significant inflammatory infiltrate. These data support the concept that malignant melanomas are capable of evoking autologous T-cell immune reactions. |
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Keywords: | Cutaneous Melanoma Monoclonal antibodies Lymphocytes |
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