Tumor-mediated immunosuppression: Prevention by inhibitors of prostaglandin synthesis |
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Authors: | Kazimiera D. Grinwich Otto J. Plescia |
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Affiliation: | Waksman Institute of Microbiology Rutgers, The State University of New Jersey P. O. Box 759, Piscataway, New JerseyUSA 08854 |
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Abstract: | The addition of MC16 tumor cells (a prostaglandin E2-producing cell line induced in C57B1/6J mice by methylcholanthrene) to cultures of normal syngeneic spleen cells inhibits the antibody response of these cells to sheep red blood cells. This inhibition can be blocked by adding to the cultures prostaglandin synthetase inhibitors, such as indomethacin, flufenamic acid and aspirin. These MC16 tumor cells are also immunosuppressive . Mice bearing the syngeneic MC16 tumor become unresponsive to sheep red blood cells as the tumor grows. As in the test system, inhibitors of prostaglandin synthetases seem to block the immunosuppressive activity of MC16 cells since tumor-bearing mice, treated therapeutically with indomethacin, responded normally in their production of antibody to sheep red blood cells. |
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Keywords: | To whom requests for reprints should be sent |
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