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膳食核酸与肠道微生物群协同促进Th1/Th2平衡向Th1偏向性免疫转变。

Dietary nucleic acid and intestinal microbiota synergistically promote a shift in the Th1/Th2 balance toward Th1-skewed immunity.

作者信息

Sudo Nobuyuki, Aiba Yuji, Oyama Naomi, Yu Xiao-Nian, Matsunaga Masaji, Koga Yasuhiro, Kubo Chiharu

机构信息

Department of Psychosomatic Medicine, Graduate School of Medical Sciences, Kyushu University, Fukuoka, Japan.

出版信息

Int Arch Allergy Immunol. 2004 Oct;135(2):132-5. doi: 10.1159/000080655. Epub 2004 Sep 2.

Abstract

BACKGROUND

Intestinal microbiota are known to play an important role in the establishment of oral tolerance, thereby protecting the organism from food allergies. Dietary intake of nucleic acid (NA) is also reported to have such an anti-allergic effect; however, one unsolved question is whether or not dietary NA would act through a process of toll-like receptor 9 signaling activated by DNA containing a CpG motif, a well-known sequence leading to immunostimulatory activity. In this study, we focused on the question of whether the addition of dietary NA lacking CpG motifs would allow continued modulation of the Th1/Th2 balance.

METHODS

Germ free (GF) and Bifidobacterium-infantis-monoassociated BALB/c mice were maintained on either an NA-free casein diet or on an NA-supplemented casein diet for 4 weeks. Thereafter, both the in vivo anti-casein antibody levels and in vitro splenocyte cytokine secretion pattern were evaluated.

RESULTS

Feeding with a casein diet elicited a substantial increase in the serum anti-casein-specific IgG1, IgG2a, and IgE levels of GF mice fed the NA free-diet. The in vitro cytokine production profile showed that enhanced IL-4 production in the GF mice fed the NA free-diet was markedly reduced by the supplementation with dietary NA in both the GF and B.-infantis-monoassociated mice. In addition, IFN-gamma secretion increased in the B.-infantis-reconstituted mice fed the diet containing NA.

CONCLUSIONS

These results suggest that dietary intake of NA devoid of CpG motifs may prevent the development of allergies via acceleration of Th1-dominant immunity.

摘要

背景

已知肠道微生物群在建立口服耐受性中起重要作用,从而保护机体免受食物过敏。据报道,饮食中摄入核酸(NA)也具有这种抗过敏作用;然而,一个尚未解决的问题是,饮食中的NA是否会通过含CpG基序的DNA激活的Toll样受体9信号传导过程起作用,CpG基序是一种导致免疫刺激活性的著名序列。在本研究中,我们关注的问题是,添加缺乏CpG基序的饮食NA是否能持续调节Th1/Th2平衡。

方法

将无菌(GF)和婴儿双歧杆菌单联的BALB/c小鼠分别用不含NA的酪蛋白饮食或补充了NA的酪蛋白饮食喂养4周。此后,评估体内抗酪蛋白抗体水平和体外脾细胞细胞因子分泌模式。

结果

用酪蛋白饮食喂养使喂食不含NA饮食的GF小鼠血清抗酪蛋白特异性IgG1、IgG2a和IgE水平大幅增加。体外细胞因子产生谱显示,在GF小鼠和婴儿双歧杆菌单联小鼠中,喂食不含NA饮食的GF小鼠中增强的IL-4产生通过补充饮食NA而显著降低。此外,在喂食含NA饮食的婴儿双歧杆菌重建小鼠中,IFN-γ分泌增加。

结论

这些结果表明,摄入不含CpG基序的饮食NA可能通过加速以Th1为主导的免疫反应来预防过敏的发生。

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