期刊文献+

血清CCL17、CXCR4与重度子痫前期患者Th17细胞的相关性分析及对母婴结局的影响 被引量:3

Correlation Analysis of Serum CCL 17,CXCR4 and Th17 Cell in Patients with Severe Pre-Eclampsia and Their Effects on Maternal and Infant Outcomes
原文传递
导出
摘要 目的:探讨血清C-C基序趋化因子配体17(CCL17)、CXC趋化因子受体4(CXCR4)与重度子痫前期(SPE)患者辅助性T细胞(Th)17细胞的相关性分析及对母婴结局的影响。方法:选择2018年3月至2021年3月苏州大学附属第二医院妇产科收治的169例SPE患者(SPE组)和77例健康孕产妇(对照组)。检测血清CCL 17、CXCR4水平和外周血Th17细胞及其细胞因子。Pearson分析血清CCL 17、CXCR4水平与外周血Th17细胞及其细胞因子的关系,多因素Logistic回归分析SPE母婴结局不良的相关因素。结果:SPE组血清CCL17、CXCR4水平低于对照组(P<0.05),外周血Th17细胞占比、血清白细胞介素(IL)-17水平高于对照组(P<0.05)。血清CCL17、CXCR4水平与外周血Th17细胞占比、血清IL-17水平呈负相关(P<0.05)。母婴结局不良53例,母婴结局良好116例,母婴结局不良组血清CCL 17、CXCR4水平低于母婴结局良好组(P<0.05)。高Th17细胞占比、年龄大、低水平CCL17、CXCR4是SPE患者母婴结局不良的危险因素(P<0.05)。结论:SPE患者血清CCL17、CXCR4水平降低,且与外周血Th17细胞占比增加,血清IL-17水平增高有关,低水平CCL17、CXCR4是SPE患者母婴结局不良的危险因素。 Objective:To investigate the correlation analysis of serum C-C chemokine ligand 17(CCL17),CXC chemokine receptor 4(CXCR4)and helper T cell(Th)17 in patients with severe pre-eclampsia(SPE)and their effects on maternal and infant outcomes.Methods:169 patients with SPE(SPE group)and 77 healthy pregnant women(control group)who were admitted to the Obstetrics and Gynecology Department of the Second Affiliated Hospital of Soochow University from March 2018 to March 2021 were selected.The serum CCL 17 and CXCR4 levels as well as peripheral blood Th17 cell and their cytokines were detected,and the maternal and infant outcomes were analyzed.The relationship between serum CCL 17 and CXCR4 levels and peripheral blood Th17 cell and their cytokines were analyzed by Pearson,and multivariate Logistic regression was used to analyze the related factors of poor maternal and infant outcomes of SPE.Results:The serum CCL17 and CXCR4 levels in the SPE group were lower than those in the control group(P<0.05),and the proportion of peripheral blood Th17 cell and the serum interleukin(IL)-17 level were higher than those in the control group(P<0.05).Serum CCL17 and CXCR4 levels were negatively correlated with the proportion of peripheral blood Th17 cell and serum IL-17 level(P<0.05).There were 53 cases with poor maternal and infant outcomes,and 116 cases with good maternal and infant outcomes.The CCL 17 and CXCR4 levels in the poor maternal and infant outcome group were lower than those in the good maternal and infant outcome group(P<0.05).High proportion of Th17 cell,old age,low CCL17 and CXCR4 level were risk factors for adverse maternal and infant outcomes in patients with SPE(P<0.05).Conclusion:The serum CCL17 and CXCR4 levels in patients with SPE are decreased,which are associated with increased proportion of peripheral blood Th17 cell,increased serum IL-17 level,and adverse maternal and infant outcomes.Low levels of CCL17 and CXCR4 are risk factors for adverse maternal and infant outcomes in patients with SPE.
作者 孙白云 蒋瑶 张荣 贾素红 凌莉 SUN Bai-yun;JIANG Yao;ZHANG Rong;JIA Su-hong;LING Li(Department of Obstetrics and Gynecology,The Second Affiliated Hospital of Suzhou University,Suzhou,Jiangsu,215000,China)
出处 《现代生物医学进展》 CAS 2023年第7期1304-1308,共5页 Progress in Modern Biomedicine
基金 省部共建放射医学与辐射防护国家重点实验室开放课题(GZK1202212)。
关键词 重度子痫前期 辅助性T细胞17 C-C基序趋化因子配体17 CXC趋化因子受体4 母婴结局 Severe pre-eclampsia Helper T cell 17 C-C chemokine ligand 17 CXC chemokine receptor 4 Maternal and infant outcomes
  • 相关文献

参考文献12

二级参考文献165

  • 1肖玲,王心,尚丽新.早发型重度子痫前期合并多器官功能障碍综合征15例回顾性分析[J].中华临床医师杂志(电子版),2012,6(20):198-200. 被引量:6
  • 2邓瀚.妊娠期高血压危险因素及其对妊娠结局的影响[J].宁夏医科大学学报,2013,35(8):931-933. 被引量:39
  • 3储子彦,陈晓萍,方晶晶.趋化因子SDF-1及受体CXCR4研究进展[J].生物学杂志,2006,23(1):11-13. 被引量:7
  • 4黄萍,杨孜,张坤,王伽略,石凌懿,叶蓉华,陈蕾.重度子前期191例严重并发症的监测[J].中国实用妇科与产科杂志,2006,22(11):828-831. 被引量:42
  • 5Ren L,Liu YQ,Zhou WH,et al.Trophoblast-derived chemokine CXCL12 promotes CXCR4 expression and invasion of human first-trimester decidual stromal cells[J].Hum Reprod,2011,27 (2):366-374.
  • 6Liao YX,Zhou CH,Zeng H,et al.The role of the CXCL12-CX-CR4/CXCR7 axis in the progression and metastasis of bone sarcomas (Review)[J].Int J Mol Med,2013,32(6):1239-1246.
  • 7Xu L,Li Y,Sun H,et al.Structural basis of the interactions between CXCR4 and CXCL12/SDF-1 revealed by theoretical approaches[J].Mol Biosyst,2013,9(8):2107-2117.
  • 8Hunger C,Odemis V,Engele J.Expression and function of the SDF-1 chemokine receptors CXCR4 and CXCR7 during mouse limb muscle development and regeneration[J].Exp Cell Res,2012,318(17):2178-2190.
  • 9Tripathi V,Kumar R,Dinda AK,et al.CXCL12-CXCR7 Signaling Activates ERK and Akt Pathways in Human Choriocarcinoma Cells[J].Cell Commun Adhes,2014 Jan 23.[Epub ahead of print].
  • 10Sanchez-Martin L,Sanchez-Mateos P,Cabanas C.CXCR7 impact on CXCL12 biology and disease[J].Trends Mol Med,2013,19 (1):12-22.

共引文献1311

同被引文献45

引证文献3

二级引证文献3

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