Department of Human Immunology, Research Institute for Frontier Medicine, Sapporo Medical University School of Medicine, Sapporo, Japan.
Department of Respiratory Medicine and Allergology, Sapporo Medical University School of Medicine, Sapporo, Japan.
Mod Rheumatol. 2021 Jan;31(1):249-260. doi: 10.1080/14397595.2020.1719576. Epub 2020 Feb 5.
The aim of this study was to determine pathological features of T peripheral helper (Tph)-like (PD-1CXCR5CD4 T) cells in IgG4-related disease (IgG4-RD).
Tph-like cells in the blood and submandibular glands (SMGs) from IgG4-RD patients were analyzed by flow cytometry. Correlations between level of a Tph-like cell subset and clinical parameters of IgG4-RD were investigated. The cytotoxic capacity of Tph-like cells was also examined. Expression profiles of a molecule related to a Tph-like cell subset in IgG4-RD SMGs were assessed by immunohistochemistry.
Tph-like cells from IgG4-RD patients highly expressed a fractalkine receptor, CX3CR1. Percentages of circulating CX3CR1 Tph-like cells were significantly correlated with clinical parameters including IgG4-RD Responder Index, number of involved organs, and serum level of soluble IL-2 receptor. CX3CR1 Tph-like cells abundantly possessed cytotoxic T lymphocyte-related molecules such as granzyme A, perforin, and G protein-coupled receptor 56. Functional assays revealed their cytotoxic potential against vascular endothelial cells and ductal epithelial cells. Immunohistochemistry showed that fractalkine was markedly expressed in vascular endothelial cells and ductal epithelial cells in IgG4-RD SMGs.
CX3CR1 Tph-like cells are thought to contribute to persistent tissue injury in IgG4-RD and are a potential clinical marker and/or therapeutic target for inhibiting progression of IgG4-RD.
本研究旨在确定 T 外周辅助(Tph-样)(PD-1+CXCR5+CD4+T 细胞)在 IgG4 相关疾病(IgG4-RD)中的病理特征。
通过流式细胞术分析 IgG4-RD 患者血液和颌下腺(SMG)中的 Tph-样细胞。研究 Tph-样细胞亚群水平与 IgG4-RD 临床参数之间的相关性。还检查了 Tph-样细胞的细胞毒性能力。通过免疫组织化学评估 IgG4-RD SMG 中与 Tph-样细胞亚群相关的分子的表达谱。
IgG4-RD 患者的 Tph-样细胞高表达趋化因子 fractalkine 受体 CX3CR1。循环 CX3CR1+Tph-样细胞的百分比与 IgG4-RD 应答指数、受累器官数量和可溶性白细胞介素 2 受体的血清水平等临床参数显著相关。CX3CR1+Tph-样细胞大量表达颗粒酶 A、穿孔素和 G 蛋白偶联受体 56 等细胞毒性 T 淋巴细胞相关分子。功能测定显示它们对血管内皮细胞和导管上皮细胞具有细胞毒性潜力。免疫组织化学显示,IgG4-RD SMG 中的 fractalkine 在血管内皮细胞和导管上皮细胞中明显表达。
CX3CR1+Tph-样细胞被认为有助于 IgG4-RD 中的持续组织损伤,是抑制 IgG4-RD 进展的潜在临床标志物和/或治疗靶点。