前沿:病变滤泡辅助性T细胞在IgG4相关疾病发病机制中的关键作用

Cutting Edge: A Critical Role of Lesional T Follicular Helper Cells in the Pathogenesis of IgG4-Related Disease.

作者信息

Kamekura Ryuta, Takano Kenichi, Yamamoto Motohisa, Kawata Koji, Shigehara Katsunori, Jitsukawa Sumito, Nagaya Tomonori, Ito Fumie, Sato Akinori, Ogasawara Noriko, Tsubomatsu Chieko, Takahashi Hiroki, Nakase Hiroshi, Himi Tetsuo, Ichimiya Shingo

机构信息

Department of Human Immunology, Research Institute for Frontier Medicine, Sapporo Medical University School of Medicine, Chuo-ku, Sapporo 060-8556, Japan;

Department of Otolaryngology, Sapporo Medical University School of Medicine, Chuo-ku, Sapporo 060-8543, Japan.

出版信息

J Immunol. 2017 Oct 15;199(8):2624-2629. doi: 10.4049/jimmunol.1601507. Epub 2017 Sep 15.

Abstract

IgG4-related disease (IgG4-RD) is a newly recognized systemic chronic fibroinflammatory disease. However, the pathogenesis of IgG4-RD remains unknown. To determine the pathophysiologic features of IgG4-RD, we examined T follicular helper (Tfh) cells in lesions and blood from patients with IgG4-RD. Patients with IgG4-related dacryoadenitis and sialadenitis (IgG4-DS) showed increased infiltration of Tfh cells highly expressing programmed death 1 and ICOS in submandibular glands. Tfh cells from IgG4-DS submandibular glands had higher expression of B cell lymphoma 6 and a greater capacity to help B cells produce IgG4 than did tonsillar Tfh cells. We also found that the percentage of programmed death 1 circulating Tfh cells in IgG4-DS patients was higher than that in healthy volunteers and was well correlated with clinical parameters. Our findings indicate that anomalous Tfh cells in tissue lesions of IgG4-RD have features distinct from those in lymphoid counterparts or blood and potentially regulate local IgG4 production in IgG4-RD.

摘要

IgG4相关疾病(IgG4-RD)是一种新认识的全身性慢性纤维炎性疾病。然而,IgG4-RD的发病机制仍不清楚。为了确定IgG4-RD的病理生理特征,我们检测了IgG4-RD患者病变组织和血液中的滤泡辅助性T细胞(Tfh)。患有IgG4相关性泪腺炎和涎腺炎(IgG4-DS)的患者下颌下腺中高表达程序性死亡1和诱导共刺激分子的Tfh细胞浸润增加。与扁桃体Tfh细胞相比,IgG4-DS下颌下腺中的Tfh细胞B细胞淋巴瘤6表达更高,且辅助B细胞产生IgG4的能力更强。我们还发现,IgG4-DS患者循环中程序性死亡1阳性Tfh细胞的百分比高于健康志愿者,且与临床参数密切相关。我们的研究结果表明,IgG4-RD组织病变中的异常Tfh细胞具有与淋巴组织或血液中的Tfh细胞不同的特征,并可能在IgG4-RD中调节局部IgG4的产生。

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