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.
| Original language | English |
|---|---|
| Pages (from-to) | 1533-1539 |
| Number of pages | 7 |
| Journal | Journal of Experimental Medicine |
| Volume | 195 |
| Issue number | 12 |
| DOIs | |
| Publication status | Published - 17 Jun 2002 |
| Externally published | Yes |
Keywords
- Cytokines
- Homeostasis
- Mice
- T lymphocytes
- Transgenic