Toll-like receptor ligands synergize through distinct dendritic cell pathways to induce T cell responses: Implications for vaccines

被引:148
作者
Zhu, Qing [1 ]
Egelston, Colt [1 ]
Vivekanandhan, Aravindhan [2 ]
Uematsu, Satoshi [3 ]
Akira, Shizuo [3 ]
Klinman, Dennis M. [2 ]
Belyakov, Igor M. [1 ]
Berzofsky, Jay A. [1 ]
机构
[1] NCI, NIH, Vaccine Branch, Ctr Canc Res, Bethesda, MD 20892 USA
[2] NCI, NIH, Expt Immunol Lab, Bethesda, MD 20892 USA
[3] Osaka Univ, Microbial Dis Res Inst, Dept Host Def, Osaka 5600043, Japan
基金
美国国家卫生研究院;
关键词
HIV; innate immunity; adjuvants; MyD88; TRIF;
D O I
10.1073/pnas.0805325105
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Toll-like receptors (TLRs) may need to cooperate with each other to be effective in detecting imminent infection and trigger immune responses. understanding is still limited about the intracellular mechanism of this cooperation. We found that when certain TLRs are involved, dendritic cells (DCs) establish unidirectional intracellular cross-talk, in which the MyD88-independent TRIF-dependent pathway amplifies the MyD88-dependent DC function through a JNK-dependent mechanism. The amplified MyD88-dependent DC function determines the induction of the T cell response to a given vaccine in vivo. Therefore, our study revealed an underlying TLR mechanism governing the functional, nonrandom interplay among TLRs for recognition of combinatorial ligands that may be dangerous to the host, providing important guidance for design of novel synergistic molecular vaccine adjuvants.
引用
收藏
页码:16260 / 16265
页数:6
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