We evaluated the cytolytic function, phenotypic characteristics, and cytokine levels of 22 patients with non-Hodgkin's lymphoma and 7 with Hodgkin's disease receiving interleukin-la (IL-1α) following autologous bone marrow or peripheral blood stem cell transplantation. IL-1α was given i.v. over 6 hr, between day 0 and day +13 posttransplant. On day +14, cells from patients receiving high-dose IL-1α (3.0 μg/m2/day) had significantly enhanced killing of natural killer (NK)-sensitive and -resistant lymphoma targets compared to those treated with low-dose IL-1α (0.1, 0.3, or 1.0 μg/m2/day). The differences in cytolytic function between the two groups persisted but were not as striking on day +28. Patients receiving higher-dose IL-1α had a significantly increased proportion of CD3+ T cells on days +14 and +28, while the proportion of CD16+ and CD56+ NK cells was decreased compared to those of patients treated with the lower dose. There were no detectable levels of IL-2, interferon-γ, or tumor necrosis factor-α in the plasma of patients receiving IL-1α posttransplant. However, higher-dose IL-1α therapy was associated with significant increases in serum IL-6 levels in comparison to those in patients receiving low-dose IL-1α. IL-1α may increase cytolytic function post-bone marrow transplantation; it remains to be determined, however, whether this would have an impact on decreasing relapse rates of patients undergoing transplantation for lymphoma.
|Original language||English (US)|
|Number of pages||7|
|Journal||Journal of Clinical Immunology|
|State||Published - May 1994|
- Interleukin-1 (IL-1)
- bone marrow transplantation