Department of Pharmacognosy, Graduate School of Pharmacy, Meijo University, Nagoya, Japan.
Department of Pharmacognosy, Faculty of Pharmacy, Meijo University, Nagoya, Japan.
Int Arch Allergy Immunol. 2022;183(1):1-13. doi: 10.1159/000518448. Epub 2021 Oct 12.
Juzentaihoto (JTT) is a Kampo prescription that has been used clinically for treating skin diseases such as atopic dermatitis in Japan. We have previously studied the anti-allergic effects of JTT on 2,4,6-trinitrochlorobenzene (TNCB)-induced contact hypersensitivity (CHS) in mice and demonstrated that it significantly suppresses ear swelling in a dose-dependent manner. However, the mechanism underlying the anti-allergic actions of JTT is obscure.
We investigated the mechanism underlying the anti-allergic effects of JTT using a TNCB-induced murine CHS model and adoptive cell transfer experiments.
We showed that the anti-allergic effects of JTT are due to inhibition of effector T-cell activation and induction and/or activation of regulatory T cells. Furthermore, ex vivo experiments confirmed the effect of JTT on the activation of effector T cells and regulatory T cells, as interferon-γ production decreased, whereas interleukin (IL)-10 production increased, in the cultured lymphocytes obtained from 5% TNCB-sensitized mice treated with anti-CD3ε and anti-CD28 monoclonal antibodies. Flow cytometry showed that the CD4+CD25+Foxp3+, CD4+CD25+Foxp3-, and CD8+CD122+ cell population increased after oral administration of JTT. Finally, the anti-allergic effect of JTT by inducing and/or activating regulatory T cells (Tregs) was confirmed to be mediated by IL-10 through in vivo neutralization experiments with anti-IL-10 monoclonal antibodies.
We suggested that JTT exerts anti-allergic effects by regulating the activation of effector T cells and Tregs involved in murine CHS model.
JT 是一种汉方药,已在临床上用于治疗特应性皮炎等皮肤病。我们之前研究了 JT 对 2,4,6-三硝基氯苯(TNCB)诱导的接触性超敏反应(CHS)的抗过敏作用,结果表明它能显著抑制耳肿胀,且呈剂量依赖性。然而,JT 的抗过敏作用机制尚不清楚。
我们采用 TNCB 诱导的小鼠 CHS 模型和过继细胞转移实验,研究 JT 的抗过敏作用机制。
我们发现 JT 的抗过敏作用是由于抑制效应 T 细胞激活以及诱导和/或激活调节性 T 细胞。此外,体外实验证实 JT 对效应 T 细胞和调节性 T 细胞的激活有影响,因为用抗 CD3ε 和抗 CD28 单克隆抗体处理 5% TNCB 致敏的小鼠培养的淋巴细胞中干扰素-γ的产生减少,而白细胞介素(IL)-10 的产生增加。流式细胞术显示,口服 JT 后 CD4+CD25+Foxp3+、CD4+CD25+Foxp3-和 CD8+CD122+细胞群增加。最后,通过体内中和实验用抗 IL-10 单克隆抗体证实,JT 通过诱导和/或激活调节性 T 细胞(Tregs)发挥抗过敏作用。
我们认为 JT 通过调节参与小鼠 CHS 模型的效应 T 细胞和 Tregs 的激活发挥抗过敏作用。