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Th2细胞和调节性免疫反应有助于IgG4的产生以及米库利奇病的发病。

Th2 and regulatory immune reactions contribute to IgG4 production and the initiation of Mikulicz disease.

作者信息

Tanaka Akihiko, Moriyama Masafumi, Nakashima Hitoshi, Miyake Katsuhisa, Hayashida Jun-Nosuke, Maehara Takashi, Shinozaki Shouichi, Kubo Yoshiaki, Nakamura Seiji

机构信息

Faculty of Dental Science, Kyushu University, Fukuoka, Japan.

出版信息

Arthritis Rheum. 2012 Jan;64(1):254-63. doi: 10.1002/art.33320.

Abstract

OBJECTIVE

Mikulicz disease has been considered to be a subtype of Sjögren's syndrome (SS). However, recent studies have suggested that Mikulicz disease is an IgG4-related disease and is distinguishable from SS. In addition, it has been reported that both interleukin-4 (IL-4) and IL-10 induce IgG4 production and inhibit IgE. This study was undertaken to examine the expression of these cytokines in patients with Mikulicz disease and patients with SS.

METHODS

Labial salivary gland (LSG) sections from 15 patients with Mikulicz disease and 18 patients with SS were examined for subsets of the infiltrating lymphocytes, expression patterns of messenger RNA (mRNA) for cytokines/chemokines, and relationships between the IgG4:IgG ratio and the expression of mRNA for IL-4 or IL-10.

RESULTS

Immunohistochemical analysis showed lymphocyte infiltration of various subsets in the LSGs of SS patients, and the selective infiltration of IgG4-positive plasma cells and Treg cells in the LSGs of Mikulicz disease patients. The levels of mRNA for both Th1 and Th2 cytokines and chemokines in LSGs from patients with SS were significantly higher than in controls, while the expression of both Th2 and Treg cells was significantly higher in the patients with Mikulicz disease than in controls. Furthermore, the expression of IL-4 or IL-10 in the LSGs was correlated with the IgG4:IgG ratio.

CONCLUSION

These results suggest that the pathogenesis of Mikulicz disease is different from that of SS. Mikulicz disease is a unique inflammatory disorder characterized by Th2 and regulatory immune reactions that might play key roles in IgG4 production.

摘要

目的

米库利奇病曾被认为是干燥综合征(SS)的一种亚型。然而,最近的研究表明,米库利奇病是一种IgG4相关疾病,可与干燥综合征相区分。此外,有报道称白细胞介素-4(IL-4)和白细胞介素-10均可诱导IgG4产生并抑制IgE。本研究旨在检测这些细胞因子在米库利奇病患者和干燥综合征患者中的表达情况。

方法

对15例米库利奇病患者和18例干燥综合征患者的唇腺组织切片进行检查,观察浸润淋巴细胞的亚群、细胞因子/趋化因子信使核糖核酸(mRNA)的表达模式,以及IgG4:IgG比值与IL-4或IL-10 mRNA表达之间的关系。

结果

免疫组织化学分析显示,干燥综合征患者唇腺中有各种亚群的淋巴细胞浸润,而米库利奇病患者唇腺中有IgG4阳性浆细胞和调节性T细胞的选择性浸润。干燥综合征患者唇腺中Th1和Th2细胞因子及趋化因子的mRNA水平显著高于对照组,而米库利奇病患者中Th2和调节性T细胞的表达显著高于对照组。此外,唇腺中IL-4或IL-10的表达与IgG4:IgG比值相关。

结论

这些结果表明,米库利奇病的发病机制与干燥综合征不同。米库利奇病是一种独特的炎症性疾病,其特征为Th2和调节性免疫反应,可能在IgG4产生中起关键作用。

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