期刊文献+

妊娠期肝内胆汁淤积症患者外周血Th1、Th2、Th17、Treg细胞变化及意义 被引量:1

下载PDF
导出
摘要 目的 :研究妊娠期肝内胆汁淤积症(ICP)患者外周血中Th1、Th2、Th17、Treg细胞数量的变化及其意义。方法:ICP患者38例,分为轻度ICP组30例及重度ICP组8例,以30例健康孕妇为对照组。采用流式细胞术检测外周血Th1、Th2、Th17、Treg细胞数量,计算Th1/Th2及Th17/Treg比值。结果:外周血中Th1细胞比例,对照组为(20.63±3.79)%,轻度ICP组为(22.60±2.08)%,重度ICP组为(26.53±2.17)%;Th2细胞比例对照组为(6.41±0.68)%,轻度ICP组为(3.80±0.75)%,重度ICP组为(2.41±0.40)%;Th17细胞比例对照组为(2.87±0.65)%,轻度ICP组为(4.36±0.98)%,重度ICP组为(7.50±1.98)%;Treg细胞比例对照组为(5.66±1.51)%,轻度ICP组为(4.43±1.05)%,重度ICP组为(2.47±0.65)%;Th1/Th2比值对照组为3.27±0.82,轻度ICP组为6.00±1.25,重度ICP组为11.27±2.13;Th17/Treg比值对照组为0.53±0.16,轻度ICP组为1.05±0.39,重度ICP组为3.18±1.05。轻度和重度ICP组患者外周血中Th1和Th17细胞比例显著高于对照组,重度ICP组明显高于轻度ICP组;轻度和重度ICP组患者Th2和Treg细胞水平显著低于对照组,重度ICP组明显低于轻度ICP组;轻度和重度ICP组外周血中Th1/Th2和Th17/Treg比值明显高于对照组,重度ICP组明显高于轻度ICP组,差异均有统计学意义(P<0.05)。结论:妊娠期肝内胆汁淤积症孕妇外周血中存在Th1/Th2、Th17/Treg免疫失衡,在发病机制中可能发挥重要作用。
出处 《交通医学》 2021年第6期631-634,共4页 Medical Journal of Communications
基金 扬州市社会发展项目(YZ2017069)。
  • 相关文献

参考文献2

二级参考文献22

  • 1Martineau M G, Raker C, Dixon P H, et al. The metabolic profile of intrahepatic cholestasis of pregnancy is asso ciated with impaired glucose tolerance, dyslipidemia, andincreased fetal growth [J]. Diabetes Care, 2015, 38:243 -248.
  • 2Williamson C, Geenes V. Intrahepatic cholestasis of pregnancy [J]. Obstet Gynecol, 2014, 124(1): 120-133.
  • 3Madazli R, Yuksel M A, Oncul M, et al. Pregnancy outcomes and prognostic factors in patients with intrahepatic cholestasis of pregnancy [J]. J Obstet Gynaecol, 2014, 10: 1-4.
  • 4Du Q L, Pan Y D, Zhang Y H, et al. Placental gene-expression profiles of intrahepatic cholestasis of pregnancy reveal involvement of multiple molecular pathways in blood vessel formation and inflammation [J]. BMC Medical Genomics, 2014, 7: 42-52.
  • 5Qian Z D, Huang L L, Zhu X M. An immunohistochemical study of CD83+ and CDla+ positive dendritic cells in the decidua of women with recurrent spontaneous abortion [J]. Eur J Med Res, 2015, 20: 2-8.
  • 6Lee W S, Lee S M, Kim M K, et al. The tryptophan metabolite 3-hydroxyanthranilic acid suppresses T cell re- sponses by inhibiting dendritic cell activation [J]. International Immunopharmacology, 2013, 17(3): 721-726.
  • 7A1-Huseini L M, Yeang H X, Hamdam J M, et al. Heme oxygenase-1 regulates dendritic cell function through modulation of p38 MAPK-CREB/ATF1 signaling [J]. J Biol Chem, 2014, 289(23): 16442-16451.
  • 8Segerer S E, Staib C, Kaemmerer U, et al. Dendritic cells: elegant arbiters in human reproduction [J]. Curt Pharm Biotechnol, 2012, 13(8), 1378-1384.
  • 9Saito S, Nakashima A, Shima T, et al. Th1/Th2/Thl7 and regulatory T-cell paradigm in pregnancy [J]. Am J Reprod Immunol, 2010, 63(6): 601-610.
  • 10Favre N, Bourdel N, Sapin V, et al. Importance of bile acids for intra-hepatie cholestasis of pregnancy [J]. Gyne- col Obstet Fertil, 2010, 38(4):293-295.

共引文献311

同被引文献14

引证文献1

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部