Fatal Leukemia in Interleukin 15 Transgenic Mice Follows Early Expansions in Natural Killer and Memory Phenotype Cd8+ T Cells

Author:

Fehniger Todd A.12,Suzuki Kazuhiro13,Ponnappan Anand1,VanDeusen Jeffrey B.12,Cooper Megan A.12,Florea Sorin M.1,Freud Aharon G.1,Robinson Michael L.4,Durbin Joan4,Caligiuri Michael A.12

Affiliation:

1. Department of Internal Medicine, Division of Hematology/Oncology, Columbus, Ohio 43210

2. Department of Molecular Virology, Immunology and Medical Genetics, Division of Human Cancer Genetics and the Comprehensive Cancer Center, The Ohio State University, Columbus, Ohio 43210

3. Department of Urology, Gunma University School of Medicine, Gunma 371-8511, Japan

4. Children's Hospital and Research Institute, Columbus, Ohio 43205

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.

Publisher

Rockefeller University Press

Subject

Immunology,Immunology and Allergy

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