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Department of Pathology and Laboratory Medicine, Hahnemann University [C-M. L., Y. S., L. C., T. O., E. F. W], and the Department of Microbiology, Thomas Jefferson University [C. E. C.], Philadelphia, Pennsylvania
We studied the antitumor effects of recombinant human interleukin 2 (HuIL-2) in DBA/2 mice which harbor L5178Y lymphoma cells in a tumor-dormant state in the peritoneal cavity and in peritoneal cell (PC) cultures prepared from such mice. Intraperitoneal injection of 10,000 to 100,000 units of HuIL-2/day for 10 days eliminated tumor cells from 3045% of the mice, whereas no mice became tumor-free in the phosphate-buffered saline-treated control group. In vitro, as little as 10 units/well HuIL-2 stimulated antitumor cytotoxic activity in PC from tumor-dormant mice, whereas HuIL-2 in concentrations up to 1,000 units/well HuIL-2 failed to stimulate cytotoxic activity in PC from normal mice. HuIL-2 directly stimulated antitumor cytotoxic activity in nonadherent but not in adherent PC cultures from tumor-dormant mice; however, treatment of whole PC from tumor-dormant mice with HuIL-2 resulted in the development of antitumor cytotoxic activity in the adherent PC population which were derived from such cultures. This suggests that the HuIL-2-treated nonadherent PC contributed to the cytotoxic activation of the adherent PC. Flow cytometric analysis of the PC from tumordormant mice revealed a polyclonal expansion of T-lymphocytes. Lyt-1+, Lyt-2+, and L3T4+ lymphocytes were all required for HuIL-2 to induce antitumor cytotoxic activity.
1 Supported by PHS Grants CA32577 and CA37438, awarded by the National Cancer Institute, HHHS, and by a grant from Hoffmann La Roche.
2 Present address: Beckman Instruments, 200 S. Kraemer Blvd., Brea, CA 92621.
3 Present address: Second Department of Surgery, Hokkaido University School of Medicine, Sapporo, Japan.
4 To whom requests for reprints should be addressed, at Department of Pathology, Hahnemann University, Broad and Vine Streets, Philadelphia, PA 19102.
Received 9/ 7/88. Revised 7/13/89. Accepted 11/27/89.
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