Immunosuppressive Effect of Quercetin on Dendritic Cell Activation and Function

被引:143
作者
Huang, Ren-Yeong [1 ,2 ]
Yu, Yen-Ling [3 ,4 ]
Cheng, Wan-Chien [2 ]
OuYang, Chun-Nan [4 ]
Fu, Earl [1 ,2 ]
Chu, Ching-Liang [3 ,4 ,5 ]
机构
[1] Natl Def Med Ctr, Grad Inst Med Sci, Sch Dent, Taipei, Taiwan
[2] Natl Def Med Ctr, Dept Periodontol, Sch Dent, Taipei, Taiwan
[3] Natl Hlth Res Inst, Vaccine Res & Dev Ctr, Miaoli, Taiwan
[4] Natl Hlth Res Inst, Immunol Res Ctr, Miaoli, Taiwan
[5] China Med Univ, Grad Inst Immunol, Taichung, Taiwan
关键词
ARYL-HYDROCARBON RECEPTOR; NF-KAPPA-B; IN-VIVO; IMMUNOSTIMULATORY FUNCTION; CONTACT HYPERSENSITIVITY; MOLECULAR-MECHANISMS; IMMUNE-RESPONSE; T-CELLS; EXPRESSION; FLAVONOIDS;
D O I
10.4049/jimmunol.0903991
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Dendritic cells (DCs) play a crucial role in linking innate and adaptive immunity. Thus, DCs have been regarded as a major target of immunosuppressants for the control of harmful immune responses. In this study, we examined the effect of quercetin, a natural flavonoid found in many vegetables and fruits, on the activation and function of mouse DCs. Quercetin effectively inhibited LPS-induced DC activation by reducing the production of proinflammatory cytokines/chemokines and the expression levels of MHC class II and costimulatory molecules. In addition, quercetin uniquely blocked endocytosis by DCs and the LPS-induced DC migration was diminished by quercetin treatment. Furthermore, quercetin abrogated the ability of LPS-stimulated DCs to induce Ag-specific T cell activation, both in vitro and in vivo. Remarkably, coadministration of quercetin with 2,4-dinitro-1-fluorobenzene prevented 2,4-dinitro-1-fluorobenzene-induced contact hypersensitivity, indicating the potential of quercetin for treating delayed-type hypersensitive diseases. Blockage of LPS-induced ERK, JNK, Akt, and NF-kappa B activation contributed to the inhibitory effect of quercetin on DCs. These results strongly suggest that quercetin may be a potent immunosuppressive agent and could be used in the prevention and therapy of chronic inflammation, autoimmunity, and transplantation via the abolishment of DC activation and function. The Journal of Immunology, 2010, 184: 6815-6821.
引用
收藏
页码:6815 / 6821
页数:7
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