Requirement of IL-7 for IL-4-producing potential of MHC class I-selected CD4(-)CD8(-) TCR alpha beta(+) thymocytes

被引:17
|
作者
LeiteDeMoraes, MD
Herbelin, A
Gombert, JM
Vicari, A
Papiernik, M
Dy, M
机构
[1] HOP NECKER ENFANTS MALAD,INSERM U25,F-75015 PARIS 15,FRANCE
[2] HOP NECKER ENFANTS MALAD,INSERM U345,F-75015 PARIS 15,FRANCE
[3] DNAX RES INST MOL & CELLULAR BIOL INC,PALO ALTO,CA 94304
关键词
granulocyte macrophage colony stimulating factor; IL-1; NK T cells; MHC class I selection; T(h)2 cells;
D O I
10.1093/intimm/9.1.73
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
IL-7 plays an important role in the growth and differentiation of T cells. We have previously reported that IL-7 induces preferential expansion of MHC class I-selected CD4(-)CD8(-)TCR alpha beta(+) thymocytes which express a skewed V-beta repertoire and are potent IL-4 producers, In this report, we provide evidence that IL-1 in combination with granulocyte macrophage colony stimulating factor can also expand this population. Yet, these cells do not share the functional characteristics of those obtained in the presence of IL-7, i.e. cytotoxic activity and high IL-4 production. These functional capacities can be acquired by adding IL-7. In conclusion, our findings demonstrate that the capacity of MHC class I-selected CD4(-)CD8(-)TCR alpha beta(+) thymocytes to produce IL-4 as well as to kill target cells is IL-7 dependent.
引用
收藏
页码:73 / 79
页数:7
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