期刊文献+

Th17细胞和Treg细胞与不明原因复发性流产的关系 被引量:14

Relationship Between Th17/Treg Cells and Unexplained Recurrent Spontaneous Abortion
原文传递
导出
摘要 目的:探讨Th17/Treg细胞在不明原因复发性流产患者外周血、子宫蜕膜组织中的变化以及Th17细胞相关细胞因子IL-17、IL-6的表达情况。方法:应用流式细胞术检测20例不明原因复发性流产患者(实验组)、20例正常早期妊娠人工流产患者(对照组)外周血、子宫蜕膜组织中Th17细胞和Treg细胞占CD4+T淋巴细胞的比例。ELISA法检测两组患者血清中IL-17和IL-6的浓度,Q-PCR检测两组患者子宫蜕膜组织中IL-17和IL-6mR-NA的表达。结果:20例实验组患者外周血、子宫蜕膜组织中Th17细胞占CD4+T淋巴细胞的比例为(1.9±0.3)%,(1.5±0.4)%,高于20例对照组患者的(1.0±0.2)%、(0.5±0.1)%,实验组患者中Treg细胞占CD4+T细胞的比例分别为(5.2±1.1)%、(7.5±1.4)%,低于对照组患者的(8.8±1.3)%、(12.1±1.3)%(P<0.01)。20例实验组患者血清及子宫蜕膜组织中IL-17和IL-6的表达水平高于对照组。结论:不明原因复发性流产患者中Treg细胞降低,Th17细胞增加并高分泌IL-17和IL-6,这可能是流产的重要原因。 Objective: To investigate the changes of the proportion and cytokine production of Th17 cells and the frequency of Treg cells in the peripheral blood and decidua in unexplained recurrent spontaneous abortion(URSA) patients.Methods: Flow cytometry was used to assess the percentages of Th17 cells and Treg cells in CD4+ T cells in the peripheral blood and decidua of 20 patients with URSA and 20 health subjects undergone artificial abortion(control subjects).ELISA and quantitative PCR were used to analyze the expression of IL-17 and IL-6 in the serum and decidua in URSA patients and control subjects.Results: URSA patients had higher percentages of Th17 cells in CD4+ T cells in the peripheral blood and decidua([1.9±0.3] % and [1.5±0.4] % respectively,vs.[1.0±0.2] % and [0.5±0.1] % respectively in control group,both P0.01).However,the percentages(all P 0.01) of Treg cells in CD4+ T cells in the peripheral blood and decidua([5.2±1.1] % and [7.5±1.4] %) in URSA groups were lower than in control subjects([8.8±1.3] % and [2.1±1.3] % respectively).The expression of IL-17 and IL-6 in the serum and decidua in URSA patients was significantly higher than in control group.Conclusion: Th17 cells might play important roles in URSA through higher IL-17 and IL-6 expression.Meanwhile Treg cells may benefit the maintenance of pregnancy.
出处 《武汉大学学报(医学版)》 CAS 北大核心 2011年第6期773-777,共5页 Medical Journal of Wuhan University
基金 湖北省自然科学基金资助项目(编号:2010CDB06204)
关键词 不明原因复发性流产 TH17细胞 TREG细胞 IL-17 IL-6 URSA Th17 Cells Treg Cells Interleukin-17 Interleukin-6
  • 相关文献

参考文献10

  • 1Trowsdale J, Betz AG. Mother's Little helpers: mech- anisms of maternal-fetal tolerance[J]. Nat Immunol, 2006, 7: 241-246.
  • 2Arruvito L, Sotelo AI, Billordo A, et al. A physiologi- cal role for inducible FOXP3 (+) Treg cells. Lessons from women with reproductive failure[J]. Clin Immu- nol, gol0, 136(3):432-441.
  • 3Bettelli E, Carrier Y, Gao W, et al. Reciprocal devel- opmental pathways for the generation of pathogenic ef- fector TH17 and regulatory T cells[J]. Nature, 2006, 441 :235-238.
  • 4Mucida D, Park Y, Kim G, et al. Reciprocal TH17 and regulatory T cell differentiation mediated by retino- ic acid[J]. Science, 2007, 317(5 835) :256-260.
  • 5Mangan PR, Harrington LE, O' Quinn DB, etal. Transforming growth factor-beta induces development of the T(H)17 lineage[J]. Nature, 2006, 441(7 090) : 231-234.
  • 6Kesselring R, Thiel A, Pries R, et al. Human Thl7 cells can he induced through head and neck cancer and have a functionalimpact on HNSCC development [J]. Br J Cancer, 2010, 103(8):1 245-1 254.
  • 7Ogura H, Murakami M, Okuyama Y, et al. Interleu- kin-17 promotes autoimmunity by triggering a positive- feedback loop via interleukin-6 induction[J]. Immuni- ty, 2008, 29, 628-636.
  • 8夏欣一,(综述),周鑫(综述),黄宇烽(审校).转录因子FOXP3与生殖研究进展[J].中华男科学杂志,2009,15(7):642-645. 被引量:3
  • 9Lohr J, Knoechel B, Wang JJ, et al. Role of IL-17 and regulatory T lymphocytes in a systemic autoimmune disease[J]. J Exp Med, 2006, 203:2 785-2 791.
  • 10Yang H, Qiu L, Di W, et al. Proportional change of CD4+ CD25+ regulatory T cells in decidua and periph- eral blood in unexplained recurrent spontaneous abor- tion patients[J]. Fertil Steril, 2008, 89: 656-661.

二级参考文献25

  • 1林其德,邱丽华.原因不明复发性流产与母-胎界面免疫耐受[J].中华妇产科杂志,2006,41(3):145-147. 被引量:26
  • 2Zhou L,Chong MM,Littman DR.Plasticity of CD4+ T cell line-age differentiation.Immunity,2009,30(5):646-655.
  • 3Josefowiez SZ,Rudensky A.Control of regulatory T cell lineage Commitment and maintenance.Immunity,2009,30(5):616-625.
  • 4Aluvihare VR,Kallikourdis M,Betz AG.Regulatory T ceLls mediate maternal tolerance to the fetus.Nat Immunol,2004,5(3):266-271.
  • 5Schubert LA,Jeffery E,Zhang Y,et al.Scudin(FOXP3) acts as a represser of transcription and regulates T cell activation.J Biol Chem,2001,276(40):37672-37679.
  • 6Lopes JE,Totgerson TR,Zieqler SF,et al.Analysis of Foxp3 vealsmultiple domains required for its function as a transcriptional repressor.J Immunol,2006,177(5):3133-3142.
  • 7Estelle B,Maryam D,Mohamed O.Foxp3 interacts with nuclear factor of activated T ceils and NF-kB to repress eytokine gene expression and effector functions of T helper cells.Proe Natl Acad Sei USA,2005,102(14):5138-5143.
  • 8Paust S,Cantor H.Regulatory T cells and autoimmune disease.Immunol Bey,2005,204:195-207.
  • 9Sakaguchi S,Yamaguchi T,Nomura T,et al.Regulatory T cells and immune tolerance.Cell.2008,133(5):775-787.
  • 10Crispin JC,Vargas MI,Alcocer-Varela J.lmmunoregnlamry T cells in autoimmunity.Autoimmun Bev,2004,3(2):45-51.

共引文献2

同被引文献239

引证文献14

二级引证文献206

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