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

被引:234
|
作者
Kieper, WC
Tan, JT
Bondi-Boyd, B
Gapin, L
Sprent, J
Ceredig, R
Surh, CD
机构
[1] Scripps Res Inst, Dept Immunol, La Jolla, CA 92037 USA
[2] La Jolla Inst Allergy & Immunol, Div Dev Immunol, San Diego, CA 92121 USA
[3] CEA, INSERM, U548, F-38054 Grenoble, France
来源
JOURNAL OF EXPERIMENTAL MEDICINE | 2002年 / 195卷 / 12期
关键词
T lymphocytes; homeostasis; cytokines; mice; transgenic;
D O I
10.1084/jem.20020067
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Transgenic (TG) mice expressing a high copy number of interleukin (IL)-7 cDNA under the control of the major histocomaptability complex (MHC) class 11 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 CD44(bi) CD 122(bi) 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 CD44(bi) CD122(bi) 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.
引用
收藏
页码:1533 / 1539
页数:7
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