• 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

短期干扰素-β治疗对多发性硬化症细胞因子的影响:IL-17 和 IL-23 的显著调节。

Effect of short-term interferon-β treatment on cytokines in multiple sclerosis: significant modulation of IL-17 and IL-23.

机构信息

Department of Neurology, Acıbadem University School of Medicine, Istanbul, Turkey.

出版信息

Cytokine. 2012 Aug;59(2):400-2. doi: 10.1016/j.cyto.2012.05.004. Epub 2012 May 30.

DOI:10.1016/j.cyto.2012.05.004
PMID:22652415
Abstract

Therapeutic effect of interferon-β (IFN-β) treatment has been associated with modulation of the balance between Th1, Th17, Th2 and regulatory T (Treg) cells, whereas the impact of disease modifying drugs on Th9-immunity in multiple sclerosis (MS) has not been studied. To investigate the short-term effects of IFN-β treatment on cytokines in MS, we determined serum levels of IL-17, IL-23, IL-10, IL-4, IFN-γ, IL-9 and TGF-β in relapsing remitting MS patients before and 2 months after IFN-β treatment by ELISA. MS patients showed increased IL-17, IL-23 and IL-4 levels and decreased IL-9 levels as compared to healthy controls. IFN-β treatment only reduced IL-17 and IL-23 levels, whereas the levels of other cytokines remained unchanged. IFN-β treatment appears to exert its earliest therapeutic effect on Th17-immunity. The influence of IL-9 on MS pathogenesis needs to be further studied.

摘要

干扰素-β(IFN-β)治疗的疗效与 Th1、Th17、Th2 和调节性 T(Treg)细胞之间平衡的调节有关,而疾病修正药物对多发性硬化症(MS)中 Th9 免疫的影响尚未得到研究。为了研究 IFN-β治疗对 MS 中细胞因子的短期影响,我们通过 ELISA 在 IFN-β治疗前和治疗后 2 个月测定了复发缓解型 MS 患者的血清中 IL-17、IL-23、IL-10、IL-4、IFN-γ、IL-9 和 TGF-β的水平。与健康对照组相比,MS 患者的 IL-17、IL-23 和 IL-4 水平升高,而 IL-9 水平降低。IFN-β治疗仅降低了 IL-17 和 IL-23 的水平,而其他细胞因子的水平保持不变。IFN-β 治疗似乎对 Th17 免疫产生最早的治疗效果。IL-9 对 MS 发病机制的影响需要进一步研究。

相似文献

1
Effect of short-term interferon-β treatment on cytokines in multiple sclerosis: significant modulation of IL-17 and IL-23.短期干扰素-β治疗对多发性硬化症细胞因子的影响:IL-17 和 IL-23 的显著调节。
Cytokine. 2012 Aug;59(2):400-2. doi: 10.1016/j.cyto.2012.05.004. Epub 2012 May 30.
2
Short-term treatment of relapsing remitting multiple sclerosis patients with interferon (IFN)-beta1B transiently increases the blood levels of interleukin (IL)-6, IL-10 and IFN-gamma without significantly modifying those of IL-1beta, IL-2, IL-4 and tumour necrosis factor-alpha.用干扰素(IFN)-β1B对复发缓解型多发性硬化症患者进行短期治疗,可使白细胞介素(IL)-6、IL-10和IFN-γ的血液水平短暂升高,而不会显著改变IL-1β、IL-2、IL-4和肿瘤坏死因子-α的水平。
Cytokine. 2000 Jun;12(6):682-7. doi: 10.1006/cyto.1999.0616.
3
Increased IL-10 mRNA and IL-23 mRNA expression in multiple sclerosis: interferon-beta treatment increases IL-10 mRNA expression while reducing IL-23 mRNA expression.多发性硬化症中白细胞介素-10信使核糖核酸和白细胞介素-23信使核糖核酸表达增加:β-干扰素治疗可增加白细胞介素-10信使核糖核酸表达,同时降低白细胞介素-23信使核糖核酸表达。
Mult Scler. 2008 Jun;14(5):622-30. doi: 10.1177/1352458507087136. Epub 2008 Apr 18.
4
[T-cell interferon-gamma, tumor necrosis factor-alpha and interleukin-6 receptor binding in patients with multiple sclerosis. Effects of interferon-beta-1b treatment].[多发性硬化症患者的T细胞干扰素-γ、肿瘤坏死因子-α和白细胞介素-6受体结合。β-1b干扰素治疗的效果]
Rev Neurol. 1999;29(10):893-9.
5
IFN-beta inhibits human Th17 cell differentiation.干扰素-β抑制人Th17细胞分化。
J Immunol. 2009 Oct 15;183(8):5418-27. doi: 10.4049/jimmunol.0803227. Epub 2009 Sep 25.
6
Time-dependent cytokine deviation toward the Th2 side in Japanese multiple sclerosis patients with interferon beta-1b.在接受β-1b干扰素治疗的日本多发性硬化症患者中,细胞因子随时间向Th2方向偏移。
J Neurol Sci. 2004 Jul 15;222(1-2):65-73. doi: 10.1016/j.jns.2004.04.012.
7
Evaluation of Th17-related cytokines and receptors in multiple sclerosis patients under interferon β-1 therapy.多发性硬化症患者接受干扰素 β-1 治疗后 Th17 相关细胞因子和受体的评估。
J Neuroimmunol. 2013 Feb 15;255(1-2):81-4. doi: 10.1016/j.jneuroim.2012.10.009. Epub 2012 Nov 21.
8
Long-term favorable response to interferon beta-1b is linked to cytokine deviation toward the Th2 and Tc2 sides in Japanese patients with multiple sclerosis.在日本多发性硬化症患者中,对β-1b干扰素的长期良好反应与细胞因子向Th2和Tc2方向偏移有关。
J Neurol Sci. 2006 Jul 15;246(1-2):71-7. doi: 10.1016/j.jns.2006.02.008. Epub 2006 Mar 6.
9
The role of endogenous IFN-β in the regulation of Th17 responses in patients with relapsing-remitting multiple sclerosis.内源性 IFN-β 在调节复发缓解型多发性硬化症患者 Th17 反应中的作用。
J Immunol. 2014 Jun 15;192(12):5610-7. doi: 10.4049/jimmunol.1302580. Epub 2014 May 21.
10
Preferential recruitment of interferon-gamma-expressing TH17 cells in multiple sclerosis.多发性硬化症中表达干扰素-γ的TH17细胞的优先募集。
Ann Neurol. 2009 Sep;66(3):390-402. doi: 10.1002/ana.21748.

引用本文的文献

1
Working in negative space: Type I interferon mediated immuno-modulation through transcriptional suppression in disease and homeostasis.负空间中的作用:I型干扰素在疾病和稳态中通过转录抑制介导免疫调节。
Innate Immun. 2025 Jan-Dec;31:17534259251367263. doi: 10.1177/17534259251367263. Epub 2025 Aug 18.
2
Targeting Th9 cells in autoimmune diseases: a narrative review.自身免疫性疾病中靶向Th9细胞:一篇叙述性综述。
Front Immunol. 2025 Jul 23;16:1615611. doi: 10.3389/fimmu.2025.1615611. eCollection 2025.
3
The Effect of Smoking and Passive Exposure on Multiple Sclerosis and Correlation with IL17 & IL23 Levels.
吸烟及被动接触对多发性硬化症的影响及其与白细胞介素17和白细胞介素23水平的相关性
Noro Psikiyatr Ars. 2025 Feb 7;62(1):54-61. doi: 10.29399/npa.28790. eCollection 2025.
4
Alterations of the Fecal Microbiota in Chinese Patients With Multiple Sclerosis.中国多发性硬化症患者粪便微生物群的改变。
Front Immunol. 2020 Dec 16;11:590783. doi: 10.3389/fimmu.2020.590783. eCollection 2020.
5
HMGB1 as a potential new marker of disease activity in patients with multiple sclerosis.高迁移率族蛋白 B1 作为多发性硬化症患者疾病活动的潜在新标志物。
Neurol Sci. 2020 Mar;41(3):599-604. doi: 10.1007/s10072-019-04136-3. Epub 2019 Nov 14.
6
Do Th17 Lymphocytes and IL-17 Contribute to Parkinson's Disease? A Systematic Review of Available Evidence.辅助性T细胞17淋巴细胞和白细胞介素-17与帕金森病有关吗?现有证据的系统评价。
Front Neurol. 2019 Jan 24;10:13. doi: 10.3389/fneur.2019.00013. eCollection 2019.
7
Cytokine Therapies in Neurological Disease.神经疾病中的细胞因子疗法
Neurotherapeutics. 2016 Jul;13(3):555-61. doi: 10.1007/s13311-016-0455-1.
8
The T helper type 17/regulatory T cell paradigm in pregnancy.孕期17型辅助性T细胞/调节性T细胞模式
Immunology. 2016 May;148(1):13-21. doi: 10.1111/imm.12595.
9
The Role of IL-17 and Th17 Lymphocytes in Autoimmune Diseases.白细胞介素-17和辅助性T细胞17在自身免疫性疾病中的作用
Arch Immunol Ther Exp (Warsz). 2015 Dec;63(6):435-49. doi: 10.1007/s00005-015-0344-z. Epub 2015 Jun 11.
10
M1 and M2 immune activation in Parkinson's Disease: Foe and ally?帕金森病中的M1和M2免疫激活:敌人还是盟友?
Neuroscience. 2015 Aug 27;302:59-73. doi: 10.1016/j.neuroscience.2014.11.018. Epub 2014 Nov 25.