• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

重度抑郁症患者 T 调节细胞功能下降:选择性 5-羟色胺再摄取抑制剂的影响。

Diminished functional properties of T regulatory cells in major depressive disorder: The influence of selective serotonin reuptake inhibitor.

机构信息

Research Center for Behavioral Disorders and Substances Abuse, Hamadan University of Medical Sciences, Hamadan, Iran.

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

出版信息

J Neuroimmunol. 2020 Jul 15;344:577250. doi: 10.1016/j.jneuroim.2020.577250. Epub 2020 Apr 23.

DOI:10.1016/j.jneuroim.2020.577250
PMID:32344162
Abstract

The properties of CD4CD25 T regulatory cells (Tregs), and interleukin (IL)-2 pathway were investigated in major depressive disorder (MDD) patients treated with or without selective serotonin reuptake inhibitor (SSRI). The frequencies of FOXP3 and pSTAT5 in peripheral Tregs were found to be diminished in untreated patients (SSRI) versus HCs (p < .001 for both), while their percentages were increased in treated patients (SSRI) versus untreated patients (p < .001 and p = .04). The proliferation of CD4 T cells was higher in SSRIMDD patients versus HCs (p = .03). The SSRIMDD patients showed a lower concentration of supernatant TGF-β than HCs (p = .001), while the production of TGF-β was enhanced in SSRIMDD versus SSRIMDD patients (p = .003). The number of CD45RA-expressing Tregs, the expression of JAK1 and JAK3, and the levels of IL-2 and IL-10 were similar between the patients and HCs. The study results showed that untreated patients have an impaired IL-2 signaling pathway and defective Tregs, and SSRI treatment may improve the Tregs function.

摘要

研究了未接受选择性 5-羟色胺再摄取抑制剂(SSRI)治疗和接受 SSRI 治疗的重度抑郁症(MDD)患者中 CD4+CD25+调节性 T 细胞(Tregs)的特性和白细胞介素(IL)-2 通路。与健康对照(HCs)相比,未经治疗的患者(SSRI)外周血 Tregs 中 FOXP3 和 pSTAT5 的频率降低(均为 p<0.001),而经治疗的患者(SSRI)的比例高于未经治疗的患者(均为 p<0.001 和 p=0.04)。与 HCs 相比,SSRI+MDD 患者的 CD4+T 细胞增殖率更高(p=0.03)。与 HCs 相比,SSRI+MDD 患者的上清液 TGF-β浓度较低(p=0.001),而 SSRI+MDD 患者的 TGF-β产生增强(p=0.003)。CD45RA 表达的 Tregs 数量、JAK1 和 JAK3 的表达以及 IL-2 和 IL-10 的水平在患者和 HCs 之间相似。研究结果表明,未经治疗的患者存在 IL-2 信号通路受损和 Tregs 功能缺陷,而 SSRI 治疗可能改善 Tregs 功能。

相似文献

1
Diminished functional properties of T regulatory cells in major depressive disorder: The influence of selective serotonin reuptake inhibitor.重度抑郁症患者 T 调节细胞功能下降:选择性 5-羟色胺再摄取抑制剂的影响。
J Neuroimmunol. 2020 Jul 15;344:577250. doi: 10.1016/j.jneuroim.2020.577250. Epub 2020 Apr 23.
2
Economic impact of therapeutic substitution of a brand selective serotonin reuptake inhibitor with an alternative generic selective serotonin reuptake inhibitor in patients with major depressive disorder.治疗性替代品牌选择性 5-羟色胺再摄取抑制剂与替代通用选择性 5-羟色胺再摄取抑制剂治疗重度抑郁症患者的经济影响。
Ann Pharmacother. 2011 Apr;45(4):441-51. doi: 10.1345/aph.1P482. Epub 2011 Mar 17.
3
Selective serotonin reuptake inhibitor attenuates the hyperresponsiveness of TLR2 and TLR4 Th17/Tc17-like cells in multiple sclerosis patients with major depression.选择性 5-羟色胺再摄取抑制剂可减轻多发性硬化症伴发重度抑郁症患者 TLR2 和 TLR4 Th17/Tc17 样细胞的高反应性。
Immunology. 2021 Mar;162(3):290-305. doi: 10.1111/imm.13281. Epub 2020 Nov 23.
4
Female sexual dysfunction in patients with major depressive disorder (MDD) treated with selective serotonin reuptake inhibitor (SSRI) and its association with serotonin 2A-1438 G/A single nucleotide polymorphisms.伴有选择性 5-羟色胺再摄取抑制剂(SSRI)治疗的重性抑郁障碍(MDD)患者的女性性功能障碍及其与 5-羟色胺 2A-1438 G/A 单核苷酸多态性的关系。
J Sex Med. 2014 Apr;11(4):1047-1055. doi: 10.1111/jsm.12452. Epub 2014 Feb 18.
5
Plasma levels of interleukin-6 and selective serotonin reuptake inhibitor response in patients with major depressive disorder.重度抑郁症患者血浆白细胞介素-6水平与选择性5-羟色胺再摄取抑制剂反应
Hum Psychopharmacol. 2013 Sep;28(5):466-70. doi: 10.1002/hup.2333. Epub 2013 Jun 30.
6
Antidepressant treatment increased serum miR-183 and miR-212 levels in patients with major depressive disorder.抗抑郁治疗可增加重性抑郁障碍患者血清 miR-183 和 miR-212 水平。
Psychiatry Res. 2018 Dec;270:232-237. doi: 10.1016/j.psychres.2018.09.025. Epub 2018 Sep 13.
7
Brain monoamine oxidase A binding in major depressive disorder: relationship to selective serotonin reuptake inhibitor treatment, recovery, and recurrence.重度抑郁症中脑单胺氧化酶A结合:与选择性5-羟色胺再摄取抑制剂治疗、康复及复发的关系
Arch Gen Psychiatry. 2009 Dec;66(12):1304-12. doi: 10.1001/archgenpsychiatry.2009.156.
8
Edivoxetine compared to placebo as adjunctive therapy to selective serotonin reuptake inhibitors in the prevention of symptom re-emergence in major depressive disorder.与安慰剂相比,度洛西汀作为选择性5-羟色胺再摄取抑制剂的辅助疗法用于预防重度抑郁症症状复发。
Curr Med Res Opin. 2015 Jun;31(6):1179-89. doi: 10.1185/03007995.2015.1037732. Epub 2015 May 6.
9
Variations in circulating cytokine levels during 52 week course of treatment with SSRI for major depressive disorder.在使用选择性5-羟色胺再摄取抑制剂(SSRI)治疗重度抑郁症的52周疗程中循环细胞因子水平的变化。
Eur Neuropsychopharmacol. 2008 Dec;18(12):917-24. doi: 10.1016/j.euroneuro.2008.08.001. Epub 2008 Sep 20.
10
Simultaneous initiation (coinitiation) of pharmacotherapy with triiodothyronine and a selective serotonin reuptake inhibitor for major depressive disorder: a quantitative synthesis of double-blind studies.三碘甲状腺原氨酸与选择性5-羟色胺再摄取抑制剂联合起始药物治疗重度抑郁症:双盲研究的定量综合分析
Int Clin Psychopharmacol. 2009 Jan;24(1):19-25. doi: 10.1097/YIC.0b013e328314dfaf.

引用本文的文献

1
Massage on the prevention of breast cancer through stress reduction and enhancing immune system.按摩通过减轻压力和增强免疫系统预防乳腺癌。
Breast Dis. 2024;43(1):119-126. doi: 10.3233/BD-249009.
2
T cell activation and deficits in T regulatory cells are associated with major depressive disorder and severity of depression.T 细胞激活和 T 调节细胞缺陷与重度抑郁症和抑郁症的严重程度有关。
Sci Rep. 2024 May 16;14(1):11177. doi: 10.1038/s41598-024-61865-y.
3
Understanding the Biological Relationship between Migraine and Depression.理解偏头痛和抑郁症之间的生物学关系。
Biomolecules. 2024 Jan 30;14(2):163. doi: 10.3390/biom14020163.
4
Research progress on the correlation between transforming growth factor- level and symptoms of depression.转化生长因子水平与抑郁症症状相关性的研究进展。
Zhejiang Da Xue Xue Bao Yi Xue Ban. 2023 Sep 25;52(5):646-652. doi: 10.3724/zdxbyxb-2023-0269.
5
Transient anxiety-and depression-like behaviors are linked to the depletion of Foxp3-expressing cells via inflammasome in the brain.短暂的焦虑和抑郁样行为与大脑中通过炎性小体导致的Foxp3表达细胞耗竭有关。
PNAS Nexus. 2023 Aug 22;2(8):pgad251. doi: 10.1093/pnasnexus/pgad251. eCollection 2023 Aug.
6
Inflammation in the pathogenesis of depression: a disorder of neuroimmune origin.炎症在抑郁症发病机制中的作用:一种神经免疫源性疾病。
Neuronal Signal. 2023 Jul 13;7(2):NS20220054. doi: 10.1042/NS20220054. eCollection 2023 Jul.
7
Once induced, it lasts for a long time: the structural and molecular signatures associated with depressive-like behavior after neonatal immune activation.一旦诱发,它会持续很长时间:新生儿免疫激活后与抑郁样行为相关的结构和分子特征。
Front Cell Neurosci. 2022 Dec 22;16:1066794. doi: 10.3389/fncel.2022.1066794. eCollection 2022.
8
Depression compromises antiviral innate immunity via the AVP-AHI1-Tyk2 axis.抑郁症通过 AVP-AHI1-Tyk2 轴损害抗病毒先天免疫。
Cell Res. 2022 Oct;32(10):897-913. doi: 10.1038/s41422-022-00689-9. Epub 2022 Jul 12.
9
Targeting the Adaptive Immune System in Depression: Focus on T Helper 17 Cells.针对抑郁症的适应性免疫系统:聚焦辅助性 T 细胞 17。
Pharmacol Rev. 2022 Apr;74(2):373-386. doi: 10.1124/pharmrev.120.000256.