The heat stable antigen (CD24) is not required for the generation of CD4+ effector and memory T cells by dendritic cells in vivo

被引:10
作者
de Heusch, M
Garzé, V
Maliszewski, C
Urbain, J
Liu, Y
Moser, M
机构
[1] Free Univ Brussels, Inst Biol & Med Mol, B-6041 Gosselies, Belgium
[2] Amgen Corp, Seattle, WA 98101 USA
[3] Ohio State Univ, Med Ctr, Dept Pathol, Columbus, OH 43210 USA
[4] Ohio State Univ, Med Ctr, Ctr Comprehens Canc, Columbus, OH 43210 USA
关键词
T-cell activation; interferon-gamma; costimulation;
D O I
10.1016/j.imlet.2004.05.009
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Previous work has established that CD24 is a costimulatory molecule for T-cell clonal expansion. Studies using CD24-/- mice demonstrated that CD24 plays a critical role in the CD28-independent immune response against virus and soluble antigens. The role of CD24 on dendritic cells (DCs) has not been reported. Here, we compare the CD24(+/+) and CD24(-/-) DCs in the induction of initial clonal expansion and elicitation of memory CD4(+) T cells in vivo. Our results demonstrate that the CD24 expressed on DCs is essential neither for the induction of initial T-cell clonal expansion nor for elicitation of memory activity of primed T cells in vivo. (C) 2004 Elsevier B.V. All rights reserved.
引用
收藏
页码:229 / 237
页数:9
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