a Hematology Disease Center, The First Affiliated Hospital of Xinjiang Medical University , Urumqi , P.R. China ; Xinjiang Uygur Autonomous Region Research Institute of Hematology, The First Affiliated Hospital of Xinjiang Medical University , Urumqi , P.R. China.
b State Key Laboratory Incubation Base of Major Diseases in Xinjiang, The First Affiliated Hospital of Xinjiang Medical University , Urumqi , P.R. China.
Hum Vaccin Immunother. 2018 Apr 3;14(4):832-838. doi: 10.1080/21645515.2017.1342913. Epub 2018 Jan 18.
The present study is to measure the expression of programmed death (PD)-1 / programmed death ligand-1 (PD-L1) negative costimulatory molecules, soluble format sPD-1 in patients with immune thrombocytopenia (ITP), and to investigate their correlation with the secretion of cytokines. A total of 35 patients with ITP were included in the present study. Twenty healthy subjects who received physical examination at our hospital were included as control group. Peripheral blood was collected from all ITP patients and healthy subjects. Flow cytometry was performed to determine the percentages of PD-1CD4T cells and PD-L1DCs in ITP patients and healthy subjects. Enzyme-linked immunosorbent assay was performed to measure the concentrations of interferon (IFN)-γ, interleukin (IL)-17 and sPD-1 in peripheral blood from ITP patients and healthy subjects. Percentages of PD-1CD4T cells and PD-L1DCs in peripheral blood from ITP patients before treatment were significantly higher than that from healthy subjects, but were not different from those after treatment. Serum concentrations of IFN-γ, IL-17 and sPD-1 in ITP patients before treatment were significantly higher than those in healthy subjects, and these concentrations were significantly reduced after treatment. The concentration of sPD-1 was positively correlated with the concentration of IFN-γ, and negatively correlated with platelet count. Percentages of PD-1CD4T cells and PD-L1DCs in ITP patients are higher than those in healthy subjects, but elevated sPD-1 concentration in the blood blocks PD-1/PD-L1 signaling pathway, leading to unaffected Th cell function. Elevated concentrations of IFN-γ and IL-17 in the blood may participate in the occurrence and development of ITP.
本研究旨在测定免疫性血小板减少症(ITP)患者程序性死亡(PD)-1/程序性死亡配体-1(PD-L1)负性共刺激分子、可溶性 PD-1(sPD-1)的表达,并探讨其与细胞因子分泌的关系。本研究共纳入 35 例 ITP 患者,同时选取 20 例于我院体检的健康者作为对照组。采集所有 ITP 患者和健康者外周血,采用流式细胞术检测 ITP 患者和健康者外周血中 PD-1CD4T 细胞和 PD-L1DCs 的比例;采用酶联免疫吸附试验检测 ITP 患者和健康者外周血中干扰素(IFN)-γ、白细胞介素(IL)-17 和 sPD-1 的浓度。治疗前 ITP 患者外周血中 PD-1CD4T 细胞和 PD-L1DCs 的比例显著高于健康者,但与治疗后无差异。治疗前 ITP 患者血清中 IFN-γ、IL-17 和 sPD-1 的浓度显著高于健康者,治疗后显著降低。sPD-1 浓度与 IFN-γ浓度呈正相关,与血小板计数呈负相关。ITP 患者外周血中 PD-1CD4T 细胞和 PD-L1DCs 的比例高于健康者,但血液中升高的 sPD-1 浓度阻断了 PD-1/PD-L1 信号通路,导致 Th 细胞功能不受影响。血液中升高的 IFN-γ和 IL-17 浓度可能参与了 ITP 的发生和发展。