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恩格列净治疗 2 型糖尿病患者后辅助性 T 细胞相关因子的变化。

Changes in T helper cell-related factors in patients with type 2 diabetes mellitus after empagliflozin therapy.

机构信息

Department of Internal Medicine, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran; Social Determinants of Health Research Center, Hamadan University of Medical Sciences, Hamadan, Iran.

Department of Immunology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.

出版信息

Hum Immunol. 2021 Jun;82(6):422-428. doi: 10.1016/j.humimm.2021.03.004. Epub 2021 Mar 24.

DOI:10.1016/j.humimm.2021.03.004
PMID:33771372
Abstract

The immune factors related to T helper (Th) 1 (T-bet, STAT1, and IFN-γ), Th17 (ROR-γt, STAT3, and IL-17), and Treg (FOXP3, STAT5, and IL-10) cells, and SOCS1/3 and the proliferation of Th cells were investigated in type 2 diabetes mellitus patients before (baseline) and after empagliflozin therapy. A total of 56 patients on metformin and gliclazide were separated into two groups: Group 1 did not receive empagliflozin (EMPA) and the Group 2 received 10 mg/day of empagliflozin for 6 months (EMPA). The expressions of T-bet, ROR-γt, FOXP3, STAT1/3/5 and SOCS1/3 were evaluated in CD4 T cells with real-time PCR. The production of IFN-γ, IL-17, and IL-10 from CD4 T cells was measured using ELISA. The proliferation of Th cells was assessed with flow cytometry. Six months of empagliflozin therapy significantly reduced the expression of ROR-γt and increased FOXP3 and STAT5 expression, compared to baseline. Production of IL-17 decreased after empagliflozin treatment, while IL-10 was enhanced in the EMPA group. Oral administration of empagliflozin or the addition of empagliflozin to the cell cultures diminished the proliferation of Th cells. Empagliflozin showed anti-inflammatory effects on Th cells by decreasing Th17-related factors, reducing proliferation capacity, and increasing Treg cell properties.

摘要

研究了 2 型糖尿病患者在接受恩格列净治疗前后与辅助性 T 细胞(Th)1(T-bet、STAT1 和 IFN-γ)、Th17(ROR-γt、STAT3 和 IL-17)和 Treg(FOXP3、STAT5 和 IL-10)细胞相关的免疫因素以及 SOCS1/3 和 Th 细胞增殖情况。将 56 名服用二甲双胍和格列齐特的患者分为两组:第 1 组未接受恩格列净(EMPA),第 2 组接受恩格列净 10mg/天治疗 6 个月(EMPA)。采用实时 PCR 评估 CD4 T 细胞中 T-bet、ROR-γt、FOXP3、STAT1/3/5 和 SOCS1/3 的表达。采用 ELISA 法测定 CD4 T 细胞 IFN-γ、IL-17 和 IL-10 的产生。采用流式细胞术评估 Th 细胞的增殖。与基线相比,恩格列净治疗 6 个月后,ROR-γt 的表达明显降低,FOXP3 和 STAT5 的表达增加。恩格列净治疗后 IL-17 的产生减少,而 EMPA 组的 IL-10 增强。口服恩格列净或在细胞培养物中添加恩格列净可降低 Th 细胞的增殖。恩格列净通过降低 Th17 相关因子、降低增殖能力和增加 Treg 细胞特性对 Th 细胞发挥抗炎作用。

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