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FOXP1在重症肌无力患者外周血B 淋巴细胞中的表达和临床意义 被引量:4

Expression and clinical significance of FOXP1 in peripheral blood B lymphcytes of patients with myasthenia gravis
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摘要 目的:探讨重症肌无力( MG)患者外周血B淋巴细胞中叉头框蛋白P1( FOXP1) mRNA表达水平和临床意义。方法收集34例MG患者及24例健康体检者(健康对照组)的静脉血样,并根据MG患者病情程度将其分为眼肌型重症肌无力( OMG)组和全身型重症肌无力( GMG)组,根据定量重症肌无力( QMG)量表评分。荧光实时定量PCR检测CD19+B细胞中FOXP1 mRNA的表达水平,流式细胞术检测外周血中CD138+浆细胞的表达频率,间接ELISA法检测血清IgG型抗乙酰胆碱受体( AChR)抗体滴度。分析OMG组和GMG组CD19+B细胞中FOXP1 mRNA的表达水平与QMG评分、CD138+浆细胞频率、抗AChR抗体滴度的相关性。结果与健康对照组相比,OMG组和GMG组外周血CD19+B细胞中FOXP1 mRNA表达水平均降低,抗AChR抗体滴度均增加,差异有统计学意义(P<0.01),且GMG组变化较OMG组更为显著(P<0.01)。 OMG组和GMG组外周血CD19+B细胞中FOXP1 mRNA的表达水平与QMG评分、CD138+浆细胞频率、抗AChR滴度均呈显著负相关。结论FOXP1在MG患者B细胞中表达减少,与临床严重程度及浆细胞频率负相关,提示FOXP1可能在B细胞向浆细胞分化中发挥负调控作用。 Objective To detect the level of FOXP1 mRNA in peripheral blood B lymphocytes of patients with my-asthenia gravis ( MG) and to explore the clinical significance of FOXP 1 in MG.Methods A total of 34 MG patients and 24 healthy subjects ( a control group ) were included into the current study .The MG patients were sub -divided into two groups:an ocular myasthenia gravis ( OMG) group and a general myasthenia gravis ( GMG) group.Both the QMG and GMG groups were scored using the quantitative MG (QMG) scale.The level of FOXP1 mRNA in CD19 +B cells was de-termined by quantitative real -time PCR.The frequencies of CD138 +plasma cells were detected by flow cytometry .The titers of anti-acetylcholine receptor (AchR)-IgG were tested by ELISA.Meanwhile, the associations between the level of FOXP1 mRNA in CD19 +B cells in the OMG and GMG groups and QMG scores , the frequencies of CD 138 +plasma cells and the titers of anti -AchR-IgG were analyzed .Results Compared with the control group , the OMG and GMG groups produced reduced levels of FOXP 1 mRNA in CD19 +B cells, increased frequencies of CD 138 +plasma cells and higher anti-AchR-IgG titers (each P〈0.01).Meanwhile, the changes in the GMG group was more remarkable than those in the OMG group (each P〈0.01).The level of FOXP1 mRNA in CD19 +B cells was negatively associated with QMG scores, CD138 +plasma cell frequency and anti -AchR -IgG titers.Conclusion The decreased expression of FOXP1 mRNA in B cells of MG patients is negatively associated with clinical severity and plasma cell frequency , indica-ting the potential role of FOXP 1 in negative regulation of the differentiation of B cells into plasma cells in the pathogenesis of MG.
出处 《徐州医学院学报》 CAS 2016年第7期441-445,共5页 Acta Academiae Medicinae Xuzhou
基金 国家自然科学基金面上项目(81571579,81072465) 江苏省“十二五”科教兴卫工程惬学重点人才项目(H201130)
关键词 重症肌无力 叉头框转录蛋白P1 B淋巴细胞 浆细胞 myasthenia gravis forkhead box protein l B cells plasma cells
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参考文献9

  • 1Gilhus NE, Skeie GO, Romi F, et al. Myasthenia gravis - au-toantibody characteristics and their implications for therapy [ J ]. Nat Rev Neurol, 2016,12(5) :259 -268.
  • 2Hu H, Wang B, Borde M, et al. Foxpl is an essential transcrip- tional regulator of B cell development [ J ]. Nat Immunol, 2006,7 (8) :819 -826.
  • 3van Keimpema M, Griineberg B, Mokry M, et al. The forkhead transcription factor FOXP1 represses human plasma cell differentia- tion [ J]. Blood, 2015, 126(18) :2098 -2109.
  • 4Zheng S, Dou C, Xin N, et al. Expression of interleukin - 22 in myasthenia gravis [ J]. Scand J Immunol, 2013,78 ( 1 ) : 98 - 107.
  • 5Christadoss P, Poussin M, Deng C. Animal models of myasthenia gravis [J]. Clin Immunol, 2000,94(2) :75 -87.
  • 6Browning JL. B cells move to centre stage: novel opportunities for autoimmune disease treatment [ J ]. Nat Rev Drug Discov, 2006,5 (7) :564 -576.
  • 7Bendelac A, Bonneville M, Kearney JF. Autoreactivity by design: innate B and T lymphocytes [ J ]. Nat Rev Immunol, 2001,1 (3) : 177 - 186.
  • 8Sagardoy A, Martinez - Ferrandis JI, Roa S, et aL Downregula- tion of FOXP1 is required during germinal center B - cell function [ J]. Blood, 2013,121 (21) :4311 -4320.
  • 9van Keimpema M, Grtineberg IJ, Mokry M, et al. FOXP1 direct- ly represses transcription of proapoptotic genes and cooperates with NF - κB to promote survival of human B ceils [J]. Blood, 2014, 124(23 ) :3431 - 3440.

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