Overexpression of Interleukin (IL)-7 Leads to IL-15–independent Generation of Memory Phenotype CD8+ T Cells

William C. Kieper(Scripps Research Institute), Joyce T. Tan(Scripps Research Institute), Brea Bondi-Boyd(Scripps Research Institute), Laurent Gapin(La Jolla Institute for Immunology), Jonathan Sprent(Scripps Research Institute), Rhodri Ceredig(Inserm), Charles D. Surh(Scripps Research Institute)
The Journal of Experimental Medicine
June 17, 2002
Cited by 280Open Access
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Abstract

Transgenic (TG) mice expressing a high copy number of interleukin (IL)-7 cDNA under the control of the major histocomaptability complex (MHC) class II promoter display a 10-20-fold increase in total T cell numbers. Here, we show that the increase in T cell numbers in IL-7 TG mice is most apparent at the level of memory phenotype CD44hi CD122hi CD8+ cells. Based on studies with T cell receptor (TCR) TG mice crossed to IL-7 TG mice, increased levels of IL-7 may provide costimulation for TCR recognition of self-MHC ligands and thus cause naive CD8+ cells to proliferate and differentiate into memory phenotype cells. In addition, a marked increase in CD44hi CD122hi CD8+ cells was found in IL-7 TG IL-15(-) mice. Since these cell are rare in normal IL-15(-) mice, the dependency of memory phenotype CD8+ cells on IL-15 can be overcome by overexpression of IL-7.


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