Helper requirements for generation of effector CTL to islet β cell antigens

被引:53
作者
Behrens, GMN
Li, M
Davey, GM
Allison, J
Flavell, RA
Carbone, FR
Heath, WR
机构
[1] Walter & Eliza Hall Inst Med Res, Immunol Div, Melbourne, Vic 3050, Australia
[2] Monash Univ, Dept Med, Ctr Inflammatory Dis, Clayton, Vic, Australia
[3] Univ Melbourne, Dept Microbiol & Immunol, Parkville, Vic, Australia
[4] Yale Univ, Immunobiol Sect, New Haven, CT 06520 USA
[5] Yale Univ, Howard Hughes Med Inst, New Haven, CT 06520 USA
关键词
D O I
10.4049/jimmunol.172.9.5420
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
We have dissected the helper requirements for converting a tolerogenic CD8 T cell response into one capable of causing destruction of the pancreatic islets. Injection of naive OVA-specific CD8 T cells into transgenic mice expressing OVA in the pancreas only resulted in islet destruction when activated CD4 Th cells were coinjected. This requirement for activated CD4 T cell help for induction of primary CD8 T cell-mediated immunity to tissue Ags contrasts recent reports suggesting that help is only important for CTL memory. Our findings show that signaling of CD40 on the dendritic cell presenting to CD8 T cells is important, but not sufficient, for induction of diabetes. Furthermore, once helpers are activated, they need not recognize Ag on the dendritic cells they license. This provides insight into the helper requirements for adoptive transfer immunotherapy of tumors and suggests key points for inhibition of CTL-mediated autoimmunity.
引用
收藏
页码:5420 / 5426
页数:7
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