Department of Physiology, College of Oriental Medicine, Kyung Hee University, Seoul 130-701, Republic of Korea.
Evid Based Complement Alternat Med. 2012;2012:647308. doi: 10.1155/2012/647308. Epub 2012 May 10.
A mouse pulmonary hypersensitivity experimental model that mimics human asthma was developed, and electroacupuncture (EA) treatment was shown to reduce allergic inflammatory processes. In addition, we also assessed whether the beneficial effects of EA on allergic asthma could be correlated with CD4(+)CD25(+)Foxp3(+) regulatory T cells (Treg). Cellular profiles and histopathologic analysis demonstrated that peribronchial and perivascular inflammatory cell infiltrates were significantly decreased in the EA-treated groups when compared to the OVA and anti-CD25 Ab-injected (Treg depletion) groups. Furthermore, total BAL cells were reduced in the EA groups when compared to other groups. Interestingly, the population of CD4(+)CD25(+)Foxp3(+)Tregs in pneumonocytes increased in EA-treated group when compared to OVA and Treg depletion groups. These results imply that EA stimulation at ST 36 may affect CD4(+)CD25(+)Foxp3(+) Treg in an OVA-induced experimental model and may enhance Treg function by suppressing other T cells and limiting the immune response.
建立了一种模拟人类哮喘的小鼠肺过敏实验模型,结果表明电针(EA)治疗可减轻过敏炎症过程。此外,我们还评估了 EA 对过敏性哮喘的有益作用是否与 CD4+CD25+Foxp3+调节性 T 细胞(Treg)有关。细胞特征和组织病理学分析表明,与卵清蛋白(OVA)和抗 CD25 Ab 注射(Treg 耗竭)组相比,EA 治疗组的支气管周围和血管周围炎症细胞浸润明显减少。此外,与其他组相比,EA 组的 BAL 总细胞数减少。有趣的是,与 OVA 和 Treg 耗竭组相比,EA 治疗组肺细胞中的 CD4+CD25+Foxp3+Treg 群体增加。这些结果表明,ST36 的 EA 刺激可能会影响 OVA 诱导的实验模型中的 CD4+CD25+Foxp3+Treg,并通过抑制其他 T 细胞和限制免疫反应来增强 Treg 功能。