Overexpression of interleukin (IL)-7 leads to IL-15-independent generation of memory phenotype CD8+ T cells

  • William C. Kieper
  • , Joyce T. Tan
  • , Brea Bondi-Boyd
  • , Laurent Gapin
  • , Jonathan Sprent
  • , Rhodri Ceredig
  • , Charles D. Surh

Research output: Contribution to a Journal (Peer & Non Peer)Articlepeer-review

250 Citations (Scopus)

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 languageEnglish
Pages (from-to)1533-1539
Number of pages7
JournalJournal of Experimental Medicine
Volume195
Issue number12
DOIs
Publication statusPublished - 17 Jun 2002
Externally publishedYes

Keywords

  • Cytokines
  • Homeostasis
  • Mice
  • T lymphocytes
  • Transgenic

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