CD4+CD3- accessory cells costimulate primed CD4 T cells through OX40 and CD30 at sites where T cells collaborate with B cells

被引:198
作者
Kim, MY [1 ]
Gaspal, FMC [1 ]
Wiggett, HE [1 ]
McConnell, FM [1 ]
Gulbranson-Judge, A [1 ]
Raykundalia, C [1 ]
Walker, LSK [1 ]
Goodall, MD [1 ]
Lane, PJL [1 ]
机构
[1] Univ Birmingham, Sch Med, Med Res Council, Ctr Immune Regulat, Birmingham B15 2TT, W Midlands, England
基金
英国惠康基金;
关键词
D O I
10.1016/S1074-7613(03)00110-9
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
In this report we identify an accessory cell that interacts with primed and memory T cells at sites where they collaborate with B cells. These cells are distinguished from conventional dendritic cells by their lack of response to FIt3 ligand and their inability to process antigen. Unlike dendritic cells, the CD4(+)CD3(-) cells have little CD80 or CD86 expression but do express high levels of the TNF ligands, OX40 ligand and CD30 ligand. We show that Th2-primed cells express the receptors for these TNF ligands and preferentially survive when cocultured with these cells. Furthermore, we show that the preferential survival of OX40(+) T cells and support of memory T cell help for B cells are linked to their association with CD4(+)CD3(-) cells in vivo.
引用
收藏
页码:643 / 654
页数:12
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