Department of Internal Medicine 3, Rheumatology and Immunology, Friedrich-Alexander-University Erlangen-Nürnberg (FAU) and Universitätsklinikum Erlangen, Erlangen, Germany.
Department of Internal Medicine 1, University of Erlangen-Nuremberg, Erlangen, Germany.
Cell Rep. 2018 Jul 3;24(1):169-180. doi: 10.1016/j.celrep.2018.06.005.
Group 2 innate lymphoid cells (ILC2s) were detected in the peripheral blood and the joints of rheumatoid arthritis (RA) patients, serum-induced arthritis (SIA), and collagen-induced arthritis (CIA) using flow cytometry. Circulating ILC2s were significantly increased in RA patients compared with healthy controls and inversely correlated with disease activity. Induction of arthritis in mice led to a fast increase in ILC2 number. To elucidate the role of ILC2 in arthritis, loss- and gain-of-function mouse models for ILC2 were subjected to arthritis. Reduction of ILC2 numbers in RORα/GATA3 and Tie2/RORα mice significantly exacerbated arthritis. Increasing ILC2 numbers in mice by IL-25/IL-33 mini-circles or IL-2/IL-2 antibody complex and the adoptive transfer of wild-type (WT) ILC2s significantly attenuated arthritis by affecting the initiation phase. In addition, adoptive transfer of IL-4/13-competent WT but not IL-4/13 ILC2s and decreased cytokine secretion by macrophages. These data show that ILC2s have immune-regulatory functions in arthritis.
采用流式细胞术在类风湿关节炎(RA)患者的外周血和关节中检测到 2 组固有淋巴细胞(ILC2),血清诱导关节炎(SIA)和胶原诱导关节炎(CIA)。与健康对照组相比,RA 患者的循环 ILC2 显著增加,且与疾病活动度呈负相关。关节炎在小鼠中的诱导导致 ILC2 数量的快速增加。为了阐明 ILC2 在关节炎中的作用,对 ILC2 的失活和功能获得性小鼠模型进行了关节炎研究。RORα/GATA3 和 Tie2/RORα 小鼠中 ILC2 数量的减少显著加重了关节炎。通过 IL-25/IL-33 微环或 IL-2/IL-2 抗体复合物增加小鼠中的 ILC2 数量,并通过影响起始阶段,显著减轻关节炎,通过野生型(WT)ILC2 的过继转移。此外,过继转移 IL-4/13 功能完整的 WT 但不是 IL-4/13 ILC2,以及减少巨噬细胞的细胞因子分泌。这些数据表明 ILC2 在关节炎中具有免疫调节功能。