Pei Zhangming, Qian Li, Miao Taolin, Wang Hongchao, Lu Wenwei, Chen Yuqing, Zhuang Qianger
State Key Laboratory of Food Science and Resources, Jiangnan University, Wuxi, China.
School of Food Science and Technology, Jiangnan University, Wuxi, China.
Front Nutr. 2024 Dec 12;11:1523842. doi: 10.3389/fnut.2024.1523842. eCollection 2024.
Food allergies manifest as systemic or digestive allergic responses induced by food allergens, and their progression has been demonstrated to be intimately associated with the host's gut microbiota. Our preceding investigation has revealed that the probiotic strains CCFM1189 and CCFM1190 possess the capability to mitigate the symptoms of food allergy in mice. However, the underlying mechanisms and material foundations through which these probiotic strains exert their effects remain enigmatic. Here, we initially compared the ameliorative effects of these two probiotic strains on food allergy mice subjected to antibiotic cocktail (ABX) treatment. It is indicated that ABX treatment was ineffective in alleviating weight loss, diarrhea, and allergic symptoms in mice, and it also inhibited the reduction of histamine and T helper cell 2 (Th2) cytokines mediated by effective strains, suggesting that effective strains must operate through the gut microbiota. Then, building upon the outcomes of prior non-targeted metabolomics studies, by quantifying the content of indoleacrylic acid (IA) in single-strain fermentation of probiotic strains and mouse feces, it was ascertained that effective strains do not synthesize IA themselves but can augment the concentration of IA in the gut by modulating the gut microbiota. Ultimately, we discovered that direct intervention with IA could mitigate diarrhea, allergic symptoms, and intestinal damage by modulating immunoglobulin E (IgE) levels, histamine, Th2 cytokines, and tight junction proteins, thereby corroborating that IA is a pivotal metabolite for the alleviation of food allergies. These observations underscore the significance of gut microbiota and metabolites like IA in the management of food allergies and hold potential implications for the development of novel therapeutic strategies.
食物过敏表现为由食物过敏原引起的全身或消化性过敏反应,并且已证明其进展与宿主的肠道微生物群密切相关。我们之前的研究表明,益生菌菌株CCFM1189和CCFM1190具有减轻小鼠食物过敏症状的能力。然而,这些益生菌菌株发挥作用的潜在机制和物质基础仍然不明。在此,我们首先比较了这两种益生菌菌株对接受抗生素鸡尾酒(ABX)治疗的食物过敏小鼠的改善效果。结果表明,ABX治疗在减轻小鼠体重减轻、腹泻和过敏症状方面无效,并且还抑制了有效菌株介导的组胺和辅助性T细胞2(Th2)细胞因子的减少,这表明有效菌株必须通过肠道微生物群发挥作用。然后,基于先前非靶向代谢组学研究的结果,通过定量益生菌菌株单菌株发酵和小鼠粪便中吲哚丙烯酸(IA)的含量,确定有效菌株自身不合成IA,但可以通过调节肠道微生物群增加肠道中IA的浓度。最终,我们发现直接干预IA可以通过调节免疫球蛋白E(IgE)水平、组胺、Th2细胞因子和紧密连接蛋白来减轻腹泻、过敏症状和肠道损伤,从而证实IA是减轻食物过敏的关键代谢物。这些观察结果强调了肠道微生物群和IA等代谢物在食物过敏管理中的重要性,并对新型治疗策略的开发具有潜在意义。