Fatal Leukemia in Interleukin 15 Transgenic Mice Follows Early Expansions in Natural Killer and Memory Phenotype Cd8+ T Cells
Летальный лейкоз у трансгенных мышей с интерлейкином-15 развивается после раннего увеличения численности естественных киллерных клеток и CD8+ Т-клеток с фенотипом клеток памяти
2001-01-15
SCID: 54.1/ewk7kqag
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CD8+ T cellsInterleukin-15Natural killer cellsT-NK leukemiaTransgenic mice
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Abstract (AI)
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.
Key Findings
1
A transgenic mouse model was engineered to overexpress IL-15 by removing posttranscriptional regulatory checkpoints.
2
IL-15 overexpression initially caused expansions of natural killer cells and memory-phenotype CD8+ T lymphocytes.
3
The findings support chronic stimulation by a proinflammatory cytokine as a mechanism contributing to leukemia development.
4
The mice subsequently developed fatal lymphocytic leukemia characterized by a T–NK phenotype.
5
The study provides evidence linking early inflammation-driven lymphocyte expansion to later malignant transformation.
Research Object
IL-15 transgenic mice with expanded NK and CD8+ T lymphocytes
Research Subject
The progression from early NK and memory-phenotype CD8+ T-cell expansions to fatal T-NK lymphocytic leukemia under chronic IL-15 stimulation
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2001-01-15
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