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   <subfield code="a">Induction of interleukin-2 receptor by tumor necrosis factor α on cultured ovarian tumor-associated lymphocytes</subfield>
   <subfield code="h">[Elektronische Daten]</subfield>
   <subfield code="c">[Constantin Ioannides, Bryan Fisk, Barbara Tomasovic, Raj Pandita, Bharat Aggarwal, Ralph Freedman]</subfield>
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   <subfield code="a">Summary: We have recently reported that autologous tumor-specific cytotoxic T lymphocyte (CTL) lines and clones can be developed from lymphocytes infiltrating ovarian malignant ascites (TAL). In this study, we investigated the biological effects of tumor necrosis factor α (TNFα) in the induction, expansion, long-term proliferation and lytic function of CD8+ TAL. TNFα up-regulated the IL-2 receptor (IL-2R) α chain (Tac antigen) on the surface of CD3+ CD8+ CD4− TAL, enhanced the proliferation of autologous tumor-specific CTL, and potentiated their lytic function in long-term cultures. Furthermore, in the induction and expansion phase of CD8+ TAL, the presence of TNFα was associated with a selective increase in CD8+ IL-2R+ (Tac+) cells, and subsequent decrease in CD4+ IL-2R+ (Tac+) cells. These results suggest that the observed facilitation of the outgrowth of CD8+ cells in TAL cultures may be due, at least in part, to the up-regulation of IL-2R, and indicate the usefulness of TNFα in the analysis of signalling in autologous tumor-reactive CTL.</subfield>
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   <subfield code="u">Department of Gynecology, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Box 67, 77 030, Houston, Texas, USA</subfield>
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   <subfield code="u">Department of Gynecology, The University of Texas M. D. Anderson Cancer Center, 1515 Holcombe Boulevard, Box 67, 77 030, Houston, Texas, USA</subfield>
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