中文English
ISSN 1001-5256 (Print)
ISSN 2097-3497 (Online)
CN 22-1108/R

留言板

尊敬的读者、作者、审稿人, 关于本刊的投稿、审稿、编辑和出版的任何问题, 您可以本页添加留言。我们将尽快给您答复。谢谢您的支持!

姓名
邮箱
手机号码
标题
留言内容
验证码

IL-35对慢加急性肝衰竭患者外周血CD8+ T淋巴细胞功能的影响

高艺 梁志军 符健

引用本文:
Citation:

IL-35对慢加急性肝衰竭患者外周血CD8+ T淋巴细胞功能的影响

DOI: 10.3969/j.issn.1001-5256.2019.09.025
详细信息
  • 中图分类号: R575.3

Influence of interleukin-35 on peripheral CD8+ T cell function in patients with acute-on-chronic liver failure

  • 摘要:

    目的观察慢加急性肝衰竭(ACLF)患者血清IL-35表达水平,评估IL-35对ACLF患者CD8+T淋巴细胞功能的影响。方法纳入2018年11月-2019年4月在海南省人民医院就诊的ACLF患者28例和健康对照者14例,采用ELISA法检测血清IL-35水平。分选外周血CD8+T淋巴细胞,使用重组人IL-35刺激培养,应用实时定量PCR法检测CD8+T淋巴细胞中穿孔素、颗粒酶B和颗粒溶素mRNA水平,流式细胞术检测CD8+T淋巴细胞中程序性死亡分子-1(PD-1)和细胞毒性T淋巴细胞相关抗原4(CTLA-4)的表达。应用直接接触和间接接触共培养系统将HLA-A2限制性CD8+T淋巴细胞与HepG2细胞共培养,加入重组人IL-35后通过检测靶细胞死亡比率和细胞因子分泌评估CD8+T淋巴细胞的细胞毒性和非细胞毒性功能的变化。符合正态分布的计量资料2组间比较采用两独立样本t检验或配对t检验;不符合正态分布的计量资料2组间比较采用Mann-Whitney U检验;相关性分析采用Spearman秩相关分析。结果 ACLF患者血清IL-35水平[72. 32(54. 04~111. 30) pg/...

     

  • [1] HAN Y, CUI LN, GUO GY. Immunotherapy for acute-onchronic liver failure[J]. J Clin Hepatol, 2017, 33 (9) :1677-1682. (in Chinese) 韩英, 崔丽娜, 郭冠亚.慢加急性肝衰竭的免疫治疗[J].临床肝胆病杂志, 2017, 33 (9) :1677-1682.
    [2] TEYMOURI M, PIRRO M, FALLARINO F, et al. IL-35, a hallmark of immune-regulation in cancer progression, chronic infections and inflammatory diseases[J]. Int J Cancer, 2018, 143 (9) :2105-2115.
    [3] Liver Failure and Artificial Liver Group, Chinese Society of Infectious Diseases, Chinese Medical Association; Severe Liver Disease and Artificial Liver Group, Chinese Society of Hepatology, Chinese Medical Association. Guideline for diagnosis and treatment of liver failure (2018) [J]. J Clin Hepatol, 2019, 35 (1) :38-44. (in Chinese) 中华医学会感染病学分会肝衰竭与人工肝学组, 中华医学会肝病学分会重型肝病与人工肝学组.肝衰竭诊治指南 (2018年版) [J].临床肝胆病杂志, 2019, 35 (1) :38-44.
    [4] LI Y, ZHANG H, LI Z, et al. Influence of the Notch signaling pathway on CD8+T lymphocyte function in patients with chronic hepatitis C[J]. J Clin Hepatol, 2018, 34 (2) :287-291. (in Chinese) 李彧, 张鸿, 李竹, 等. Notch信号通路对慢性丙型肝炎患者CD8+T淋巴细胞功能的影响[J].临床肝胆病杂志, 2018, 34 (2) :287-291.
    [5] WANG HM, ZHANG XH, FENG MM, et al. Interleukin-35suppresses the antitumor activity of T cells in patients with non-small cell lung cancer[J]. Cell Physiol Biochem, 2018, 47 (6) :2407-2419.
    [6] ZHANG J, ZHANG Y, WANG Q, et al. Interleukin-35 in immune-related diseases:Protection or destruction[J]. Immunology, 2019, 157 (1) :13-20.
    [7] DAMO M, JOSHI NS. Treg cell IL-10 and IL-35 exhaust CD8+T cells in tumors[J]. Nat Immunol, 2019, 20 (6) :674-675.
    [8] TENG DK, LIU Y, LV YF, et al. Elevated interleukin-35 suppresses liver inflammation by regulation of T helper 17 cells in acute hepatitis B virus infection[J]. Int Immunopharmacol, 2019, 70:252-259.
    [9] SHAO X, MA J, JIA S, et al. Interleukin-35 suppresses antiviral immune response in chronic hepatitis B virus infection[J]. Front Cell Infect Microbiol, 2017, 7:472.
    [10] LIU S, ZHANG Q, SHAO X, et al. An immunosuppressive function of interleukin-35 in chronic hepatitis C virus infection[J]. Int Immunopharmacol, 2017, 50:87-94.
    [11] FU YP, YI Y, CAI XY, et al. Overexpression of interleukin-35associates with hepatocellular carcinoma aggressiveness and recurrence after curative resection[J]. Br J Cancer, 2016, 114 (7) :767-776.
    [12] CHEN L, LUO EP, HUANG XP, et al. Expression of IL-35 in patients with acute-on-chronic liver failure and its clinical significances[J]. J Practical Med, 2013, 29 (17) :2800-2802. (in Chinese) 陈丽, 罗二平, 黄小平, 等.乙型慢加亚急性肝衰竭患者血清白细胞介素-35的表达及其临床意义[J].实用医学杂志, 2013, 29 (17) :2800-2802.
    [13] DURGEAU A, VIRK Y, CORGNAC S, et al. Recent advances in targeting CD8 T-Cell immunity for more effective cancer immunotherapy[J]. Front Immunol, 2018, 9:14.
    [14] LIU MX, LIU QY, LIU Y, et al. Interleukin-35 suppresses antitumor activity of circulating CD8+T cells in osteosarcoma patients[J]. Connect Tissue Res, 2019, 60 (4) :367-375.
    [15] ZHENG XF, HU XY, FANG H, et al. Interleukin-35 attenuates D-galactosamine/lipopolysaccharide-induced liver injury via enhancing interleukin-10 production in Kupffer cells[J].Front Pharmacol, 2018, 9:959.
    [16] WANG W, GUO H, LI H, et al. Interleukin-35 gene-modified mesenchymal stem cells protect concanavalin a-induced fulminant hepatitis by decreasing the interferon gamma level[J]. Hum Gene Ther, 2018, 29 (2) :234-241.
  • 加载中
计量
  • 文章访问数:  379
  • HTML全文浏览量:  77
  • PDF下载量:  107
  • 被引次数: 0
出版历程
  • 收稿日期:  2019-05-27
  • 出版日期:  2019-09-20
  • 分享
  • 用微信扫码二维码

    分享至好友和朋友圈

目录

    /

    返回文章
    返回