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Disodium cromoglycate treatment reduces T(H)2 immune response and immunohistopathological features in a murine model of Eosinophilic Esophagitis

机译:二冠甘露糖类处理减少了嗜酸性食道炎的小鼠模型中的T(H)2免疫应答和免疫疗法特征

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Eosinophilic esophagitis (EoE) is an emergent chronic disease of the esophagus. The immunopathological process in EoE is characterized by Th-2 immune response and prominent eosinophilic influx, in response to common food allergens. The classical treatment consists of allergen elimination diet and systemic/topical corticosteroid therapy. Nevertheless, patients do not always comply to treatment, and the prolonged corticosteroid therapy can cause side effects, therefore, there is an immediate need for new therapeutic approach for EoE. Disodium cromoglicate (DSCG) is a substance broadly used in allergic asthma treatment, and a well-known mast cell activation stabilizer. However, its effect in EoE have not been evaluated yet. This study aimed to assess the effects of DSCG treatment in an EoE experimental model. Male Balb/C mice were subcutaneously sensitized for five days with OVA, and subsequently orally OVA-challenged, DSCG administration was performed between the OVA-challenges. DSCG treatment not only reduced eosinophilic and mast cell influx, as well as reduced fibrosis. In addition, tslp, GATA(3), IL-5, FoxP(3) and IL-10 mRNA expression were reduced in esophageal mucosa, associated with lower Th2 (CD3(+)CD4(+)GATA3(+)IL4(+)) and B cells (CD19(+)CD40(+)) number in peripheral lymphoid organs. In conclusion, the data demonstrate DSCG treatment was effective in reducing mast cell activation and Th2 immune response, important immunopathological EoE features. Therefore, the use of DSCG as an EoE treatment can be considered a promising therapeutic approach to treat this disease.
机译:嗜酸性食管炎(EOE)是食管的紧急慢性疾病。 EOE中的免疫病理过程的特征在于Th-2免疫应答和突出的嗜酸性膨胀,以应对常见的食物过敏原。古典治疗包括过敏原消除饮食和全身/局部皮质类固醇治疗。然而,患者并不总是遵守治疗,并且延长的皮质类固醇治疗可能导致副作用,因此,立即需要新的eoe治疗方法。二氢钴(DSCG)是广泛用于过敏性哮喘处理的物质,以及众所周知的桅杆细胞活化稳定剂。然而,它尚未评估其在eoe中的效果。本研究旨在评估DSCG治疗在EOE实验模型中的影响。雄性BALB / C小鼠用OVA皮下敏化,然后在OVA攻击之间进行DSCG施用,随后口服OVA攻击。 DSCG治疗不仅减少了嗜酸性嗜纤度和桅杆细胞流入,以及减少纤维化。另外,与下Th2(CD3(+)CD4(+)IL4(+)相关的​​食管粘膜(CD3(+)CD4(+)IL4(+ ))和B细胞(CD19(+)CD40(+))在外周淋巴结器官中数。总之,数据证明DSCG治疗可有效降低肥大细胞活化和TH2免疫应答,重要免疫病理eoE特征。因此,使用DSCG作为EOE治疗可以被认为是治疗这种疾病的有希望的治疗方法。

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