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      Infiltrating lymphocytes and antigen expression in uveal melanoma.

      Ophthalmic research
      Adult, Aged, Antibodies, Monoclonal, Antigens, Neoplasm, analysis, Flow Cytometry, Histocompatibility Antigens Class I, immunology, Histocompatibility Antigens Class II, Humans, Immunophenotyping, Melanoma, pathology, Middle Aged, Monocytes, T-Lymphocyte Subsets, Uveal Neoplasms

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          Abstract

          Monoclonal antibodies and flow cytometry were used to study lymphocyte, monocyte and tumor cell antigen expression in uveal melanoma. Forty-one melanomas were studied after various forms of treatment. An antimelanoma antibody, 13A3E, stained 81.7% of the cells. Tumors treated with helium ions or 125I plaques had 13A3E staining reduced to 62.5%, p = 0.011. HLA-A,B,C stained 85.4%, and HLA-DR stained 7.0% of the cells. T cells (CD3 positive) comprised 4.5% (range 0.1-29.2%) of total cell population. Natural killer (NK) cells, B cells and macrophages were present in small numbers (mean less than 2.5% in each case). Tumors with numerous T cells (greater than 5%), were used for T cell subtype studies. The mean helper/inducer (CD4) to cytotoxic/suppressor (CD8) ratio was 1.00 (range 0.11-3.15). CD8 decreased, and CD4 increased with age in unirradiated tumors (p less than 0.02).

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