Abstract
Inflammation likely has a role in the early genesis of certain malignancies. Interleukin (IL)-15, a proinflammatory cytokine and growth factor, is required for lymphocyte homeostasis. Intriguingly, the expression of IL-15 protein is tightly controlled by multiple posttranscriptional mechanisms. Here, we engineered a transgenic mouse to overexpress IL-15 by eliminating these posttranscriptional checkpoints. IL-15 transgenic mice have early expansions in natural killer (NK) and CD8+ T lymphocytes. Later, these mice develop fatal lymphocytic leukemia with a T-NK phenotype. These data provide novel evidence that leukemia, like certain other cancers, can arise as the result of chronic stimulation by a proinflammatory cytokine.
Original language | English (US) |
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Pages (from-to) | 219-231 |
Number of pages | 13 |
Journal | Journal of Experimental Medicine |
Volume | 193 |
Issue number | 2 |
DOIs | |
State | Published - Jan 15 2001 |
Externally published | Yes |
All Science Journal Classification (ASJC) codes
- Immunology and Allergy
- Immunology
Keywords
- Inflammation
- Interleukin 15
- Leukemia
- Lymphocytes
- Transgenic mice