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)