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代谢应激在体内增强体液反应,且独立于炎性小体和炎症反应。

Metabolic stress boosts humoral responses in vivo independently of inflammasome and inflammatory reaction.

作者信息

Andris Fabienne, Denanglaire Sébastien, Baus Erika, Rongvaux Anthony, Steuve Jonathan, Flavell Richard A, Leo Oberdan

机构信息

Laboratoire d'Immunobiologie, Institut de Biologie et de Médecine Moléculaire, Université Libre de Bruxelles, Gosselies, Belgium.

出版信息

J Immunol. 2011 Feb 15;186(4):2245-53. doi: 10.4049/jimmunol.1002333. Epub 2011 Jan 19.

Abstract

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-β-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.

摘要

佐剂配方通过多种尚未完全阐明的途径发挥作用,从而增强体液免疫反应。在本研究中,我们发现,与T细胞依赖性抗原共同注射时,寡霉素或5-氨基咪唑-4-甲酰胺-1-β-D-核糖核苷(AICAR)可增强抗体产生。寡霉素和AICAR导致细胞内ATP减少,这表明免疫细胞可能感知到代谢应激并导致体液免疫反应增强。AICAR可促进初始Th细胞产生IL-4和IL-21,但在体外或体内均不影响树突状细胞的激活/成熟。因此,AICAR或寡霉素的佐剂作用在体内不需要MyD88或caspase-1表达。由于AICAR在人体内耐受性良好,这种化合物可能代表一种新型且安全的佐剂,在体内以最小的反应原性促进体液免疫反应。

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