Document 0651 DOCN M9620651 TI A B7-1-transfected human melanoma line stimulates proliferation and cytotoxicity of autologous and allogeneic lymphocytes. DT 9602 AU Sule-Suso J; Arienti F; Melani C; Colombo MP; Parmiani G; Division of Experimental Oncology D, Istituto Nazionale Tumori,; Milan, Italy. SO Eur J Immunol. 1995 Oct;25(10):2737-42. Unique Identifier : AIDSLINE MED/96062018 AB B7 co-stimulation is necessary to activate resting T cells upon antigen recognition by the T cell receptor. To see whether expression of B7 may render human melanoma cells able to stimulate T cells, a cloned melanoma line (Me1B6), which did not express B7-1, was transfected with the human B7-1 gene. In proliferation assays, B7-1 transfected cells (Me1B6/B7) showed greater stimulatory activity of allogeneic and autologous peripheral blood lymphocytes (PBL) compared to parental, non-transfected tumor cells. This effect was also seen when allogeneic CD8+ and CD4+ subpopulations were used as effectors. In these studies, activation of lymphocytes was B7-1-dependent and HLA classes I and II mediated. The higher proliferation correlated with an increased lytic activity by PBL stimulated with B7-1+ tumor cells against the untransfected Me1B6. Furthermore, PBL from a metastatic melanoma patient stimulated by Me1B6/B7 developed an higher lytic activity not only against Me1B6 but also against their autologous, B7-1- tumor. Finally, after Me1B6/B7 stimulation, PBL released interleukin (IL)-2 and interferon-gamma, but not IL-4, suggesting a Th1-mediated response. These data support the use of B7-1 transfected melanoma cells in the therapeutic vaccination of melanoma patients. DE Antigens, CD80/GENETICS/*PHYSIOLOGY Cell Division Cells, Cultured Cytotoxicity Tests, Immunologic *Cytotoxicity, Immunologic Haplotypes Human HLA Antigens/IMMUNOLOGY Interferon Type II/SECRETION Interleukin-2/SECRETION Lymphocyte Culture Test, Mixed *Lymphocyte Transformation Melanoma/*IMMUNOLOGY/PATHOLOGY Neoplasm Metastasis Skin Neoplasms/*IMMUNOLOGY/PATHOLOGY Support, Non-U.S. Gov't T-Lymphocytes/*IMMUNOLOGY Th1 Cells/IMMUNOLOGY Transfection Tumor Cells, Cultured Vaccination JOURNAL ARTICLE SOURCE: National Library of Medicine. NOTICE: This material may be protected by Copyright Law (Title 17, U.S.Code).