Anti‐IgE effect of small‐molecule‐compound arctigenin on food allergy in association with a distinct transcriptome profile

免疫球蛋白E 食物过敏 外周血单个核细胞 免疫学 过敏 牛蒡 花生过敏 化学 生物 生物化学 体外 抗体 医学 传统医学
作者
Mingzhuo Cao,Changda Liu,Kamal Srivastava,Adora Lin,Christopher A. Lazarski,Lu Wang,Anish Maskey,Ying Song,Xiaoke Chen,Nan Yang,Linda Zambrano,Renna Bushko,Anna Nowak‐Węgrzyn,Amanda Cox,Zhi‐Gang Liu,Weihua Huang,David Dunkin,Mingsan Miao,Xiu‐Min Li
出处
期刊:Clinical & Experimental Allergy [Wiley]
卷期号:52 (2): 250-264 被引量:6
标识
DOI:10.1111/cea.14048
摘要

Excessive production of IgE plays a major role in the pathology of food allergy. In an attempt to identify anti-IgE natural products, Arctium Lappa was one of the most effective herbs among approximately 300 screened medicinal herbs. However, little is known about its anti-IgE compounds.To identify compounds from Arctium Lappa for targeted therapy on IgE production and explore their underlying mechanisms.Liquid-liquid extraction and column chromatographic methods were used to purify the compounds. IgE inhibitory effects were determined on IgE-producing human myeloma U266 cells, peanut-allergic murine model and PBMCs from food-allergic patients. Genes involved in IgE inhibition in PBMCs were studied by RNA sequencing.The main compounds isolated were identified as arctiin and arctigenin. Both compounds significantly inhibited IgE production in U266 cells, with arctigenin the most potent (IC50=5.09μg/mL). Arctigenin (at a dose of 13 mg/kg) markedly reduced peanut-specific IgE levels, blocked hypothermia and histamine release in a peanut-allergic mouse model. Arctigenin also significantly reduced IgE production and Th2 cytokines (IL-5, IL-13) by PBMCs. We found 479 differentially expressed genes in PBMCs with arctigenin treatment (p < .001 and fold-change ≥1.5), involving 24 gene ontology terms (p < .001, FDR <0.05); cell division was the most significant. Eleven genes including UBE2C and BCL6 were validated by qPCR.Arctigenin markedly inhibited IgE production in U266 cells, peanut-allergic murine model and PBMCs from allergic patients by down-regulating cell division, cell cycle-related genes and up-regulating anti-inflammatory factors.
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