Metabolic Stress Boosts Humoral Responses In Vivo Independently of Inflammasome and Inflammatory Reaction

被引:7
作者
Andris, Fabienne [1 ]
Denanglaire, Sebastien [1 ]
Baus, Erika [1 ]
Rongvaux, Anthony [2 ]
Steuve, Jonathan [1 ]
Flavell, Richard A. [2 ,3 ]
Leo, Oberdan [1 ]
机构
[1] Univ Libre Bruxelles, Immunobiol Lab, Inst Biol & Med Mol, B-6041 Gosselies, Belgium
[2] Yale Univ, Sch Med, Dept Immunobiol, New Haven, CT 06520 USA
[3] Yale Univ, Sch Med, Howard Hughes Med Inst, New Haven, CT 06520 USA
关键词
ACTIVATED PROTEIN-KINASE; FOLLICULAR-HELPER-CELLS; NALP3; INFLAMMASOME; T-CELLS; DENDRITIC CELLS; AICA-RIBOSIDE; 5-AMINOIMIDAZOLE-4-CARBOXAMIDE RIBONUCLEOSIDE; CUTTING EDGE; METFORMIN; ALUMINUM;
D O I
10.4049/jimmunol.1002333
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
071005 [微生物学]; 100108 [医学免疫学];
摘要
Adjuvant formulations boost humoral responses by acting through several, yet incompletely elucidated pathways. In this study, we show that oligomycin or 5-aminoimidazole-4-carboxamide-1-beta-D-ribonucleoside (AICAR) enhances Ab production when coinjected with T cell-dependent Ags. Oligomycin and AICAR lead to intracellular ATP reduction, suggesting that metabolic stress could be sensed by immune cells and leads to increased humoral responses. AICAR promotes IL-4 and IL-21 by naive Th cells but does not affect dendritic cell activation/maturation in vitro or in vivo. Accordingly, the adjuvant effect of AICAR or oligomycin does not require MyD88 or caspase-1 expression in vivo. Because AICAR is well tolerated in humans, this compound could represent a novel and safe adjuvant promoting humoral responses in vivo with a minimal reactogenicity. The Journal of Immunology, 2011, 186: 2245-2253.
引用
收藏
页码:2245 / 2253
页数:9
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