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
Todd A. Fehniger, Kazuhiro Suzuki, Anand Ponnappan, Jeffrey VanDeusen, Megan A. Cooper, Sorin M. Florea, Aharon G. Freud, Michael L. Robinson, Joan E. Durbin, Michael A. Caligiuri
2001-01-15

CD8+ T cellsInterleukin-15Natural killer cellsT-NK leukemiaTransgenic mice
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.
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.

IL-15 transgenic mice with expanded NK and CD8+ T lymphocytes

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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Todd A. Fehniger
Kazuhiro Suzuki
Anand Ponnappan
Jeffrey VanDeusen
Megan A. Cooper
Sorin M. Florea
Aharon G. Freud
Michael L. Robinson
Joan E. Durbin
Michael A. Caligiuri
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