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救心丹通过抑制效应 T 细胞的活化,并在接触性超敏反应的小鼠模型中诱导和/或激活调节性 T 细胞,发挥抗过敏作用。

Juzentaihoto Exerts Anti-Allergic Effects by Inhibiting Effector T-Cell Activation and Inducing and/or Activating Regulatory T Cells in a Murine Model of Contact Hypersensitivity.

机构信息

Department of Pharmacognosy, Graduate School of Pharmacy, Meijo University, Nagoya, Japan.

Department of Pharmacognosy, Faculty of Pharmacy, Meijo University, Nagoya, Japan.

出版信息

Int Arch Allergy Immunol. 2022;183(1):1-13. doi: 10.1159/000518448. Epub 2021 Oct 12.

Abstract

BACKGROUND

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.

METHODS

We investigated the mechanism underlying the anti-allergic effects of JTT using a TNCB-induced murine CHS model and adoptive cell transfer experiments.

RESULTS

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.

CONCLUSION

We suggested that JTT exerts anti-allergic effects by regulating the activation of effector T cells and Tregs involved in murine CHS model.

摘要

背景

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。

方法

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。

结果

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。

结论

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。

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