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移植物抗宿主病中中间型单核细胞的增加:与 MDR1 Th17.1 水平的相关性以及泼尼松龙和 1α,25-二羟维生素 D3 的作用。

Increase of Intermediate Monocytes in Graft-versus-Host Disease: Correlation with MDR1Th17.1 Levels and the Effect of Prednisolone and 1α,25-Dihydroxyvitamin D3.

机构信息

Children's Hospital, University of Tuebingen, Germany.

Institute of Immunology, University of Muenster, Germany.

出版信息

Biol Blood Marrow Transplant. 2017 Dec;23(12):2057-2064. doi: 10.1016/j.bbmt.2017.08.008. Epub 2017 Aug 12.

Abstract

Graft-versus-host disease (GVHD) remains one of the major complications after allogeneic hematopoietic stem cell transplantation that is mainly treated with glucocorticoids such as prednisolone. In this study the influence of monocyte subpopulations, prednisolone, and 1α,25-dihydroxyvitamin D3 (1α,25-(OH)D3) on the induction of a proinflammatory subset of Th17 cells (MDRTh17.1) characterized by CCR6CXCR3CCR4CCR10CD161 and stable expression of the multidrug resistance protein type 1 (MDR1) was investigated. Our results demonstrate that intermediate monocytes are increased in patients with acute GVHD, promoting the induction of proinflammatory MDR1Th17.1 cells. Furthermore, prednisolone induces the development of MDR1Th17.1 cells, whereas 1α,25-(OH)D3 acts as an anti-inflammatory, leading to diminished percentages of proinflammatory MDR1Th17.1 cells in the presence of prednisolone after stimulation with the TLR4-ligand S100A8/S100A9. Moreover, 1α,25-(OH)D3 decreased the expression level of the targets JAK2 and CD74, both associated with T cell activation, in monocytes. Thus, in steroid-resistant GVHD, 1α,25-(OH)D3 could be an important regulator in monocyte-induced development of proinflammatory MDR1Th17.1 cells and might therefore be a potential therapeutic agent in combination with glucocorticoids for GVHD treatment.

摘要

移植物抗宿主病(GVHD)仍然是异基因造血干细胞移植后主要并发症之一,主要用泼尼松龙等糖皮质激素治疗。在这项研究中,研究了单核细胞亚群、泼尼松龙和 1α,25-二羟维生素 D3(1α,25-(OH)D3)对诱导表达 CCR6、CXCR3、CCR4、CCR10、CD161 和多药耐药蛋白 1(MDR1)稳定表达的促炎 Th17 细胞(MDRTh17.1)的影响。我们的研究结果表明,急性 GVHD 患者中间单核细胞增多,促进了促炎 MDR1Th17.1 细胞的诱导。此外,泼尼松龙诱导 MDR1Th17.1 细胞的发育,而 1α,25-(OH)D3 作为抗炎剂,在刺激 TLR4 配体 S100A8/S100A9 后,与泼尼松龙一起存在时,导致促炎 MDR1Th17.1 细胞的比例减少。此外,1α,25-(OH)D3 降低了单核细胞中与 T 细胞激活相关的靶点 JAK2 和 CD74 的表达水平。因此,在类固醇耐药性 GVHD 中,1α,25-(OH)D3 可能是单核细胞诱导促炎 MDR1Th17.1 细胞发育的重要调节剂,因此可能是与糖皮质激素联合治疗 GVHD 的潜在治疗剂。

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