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The cross-priming APC requires a Rel-dependent signal to induce CTL
被引:14
作者:

Mintern, JD
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机构: PO Royal Melbourne Hosp, Walter & Eliza Hall Inst, Div Immunol, Parkville, Vic, Australia

Belz, G
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h-index: 0
机构: PO Royal Melbourne Hosp, Walter & Eliza Hall Inst, Div Immunol, Parkville, Vic, Australia

Gerondakis, S
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h-index: 0
机构: PO Royal Melbourne Hosp, Walter & Eliza Hall Inst, Div Immunol, Parkville, Vic, Australia

Carbone, FR
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机构: PO Royal Melbourne Hosp, Walter & Eliza Hall Inst, Div Immunol, Parkville, Vic, Australia

Heath, WR
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机构:
PO Royal Melbourne Hosp, Walter & Eliza Hall Inst, Div Immunol, Parkville, Vic, Australia PO Royal Melbourne Hosp, Walter & Eliza Hall Inst, Div Immunol, Parkville, Vic, Australia
机构:
[1] PO Royal Melbourne Hosp, Walter & Eliza Hall Inst, Div Immunol, Parkville, Vic, Australia
[2] Univ Melbourne, Dept Microbiol & Immunol, Parkville, Vic 3052, Australia
[3] Royal Brisbane Hosp, Queensland Inst Med Res, Cooperat Res Ctr Vaccine Technol, Herston, Qld, Australia
关键词:
D O I:
10.4049/jimmunol.168.7.3283
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Induction of OVA-specific CTL by cross-priming requires help from CD4 T cells, which use CD154 to signal CD40 on the APC. To further dissect the molecular pathways involved in cross-priming, we examined the role of Rel, an NF-kappaB family member. c-rel(-/-) mice failed to generate OVA-specific CTL by cross-priming, but could induce CTL to HSV-1. Using chimeric mice, Rel expression was shown to be required by the APC, but not by the T cells. Notably, the deficiency in Rel could be overcome by triggering CD40, implying that the APC required Rel before receipt of the CD40 signal. These data suggest that the cross-priming APC must receive two signals before it can stimulate CTL. The first signal is Rel dependent and is required before activation of CD4 helper T cells, which then deliver the second signal using CD154 to trigger CD40.
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页码:3283 / 3287
页数:5
相关论文
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