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肺炎支原体肺炎患儿T淋巴细胞亚群变化的临床意义
引用本文:高劲,邰海服,薛妹,严颜,徐国成. 肺炎支原体肺炎患儿T淋巴细胞亚群变化的临床意义[J]. 皖南医学院学报, 2014, 0(6): 499-500
作者姓名:高劲  邰海服  薛妹  严颜  徐国成
作者单位:皖南医学院附属弋矶山医院儿科,安徽芜湖241001
摘    要:目的:检测肺炎支原体肺炎(MPP)患儿机体细胞免疫功能的变化,为MPP免疫学治疗提供进一步依据。方法:选取2013年712月于本院确诊为MPP的患儿60例,对照组为同期门诊体检健康儿童60例,分别检测两组儿童外周静脉血中T淋巴细胞亚群的表达水平。结果:MPP组患儿的CD3+、CD4+、CD8+、CD4+/CD8+表达水平(x珋±s,%)分别为69.12±8.07、37.76±8.22、27.96±9.28、1.53±0.56。与健康对照组儿童相比,MPP组患儿的CD3+、CD4+、CD4+/CD8+表达水平显著下降,而CD8+表达水平则显著升高(P<0.01)。结论:MPP患儿T淋巴细胞亚群表达失调,细胞免疫功能紊乱可能在MPP发病过程中起着重要作用。

关 键 词:肺炎支原体肺炎  T淋巴细胞亚群  细胞免疫

Significance of T lymphocyte subsets variation in children with mycoplasma pneumoniae pneumonia
GAO Jin,TAI Haifu,XUE Mei,YAN Yan,XU Guocheng. Significance of T lymphocyte subsets variation in children with mycoplasma pneumoniae pneumonia[J]. Acta Academiae Medicinae Wannan, 2014, 0(6): 499-500
Authors:GAO Jin  TAI Haifu  XUE Mei  YAN Yan  XU Guocheng
Affiliation:(Department of Pediatrics, Yijishan Hospital, Wannan Medical College, Wuhu 241001, China)
Abstract:Objective:To detect the changes of T lymphocyte subsets in children with mycoplasma pneumoniae pneumonia ( MPP) for basis with immuno-logical therapy for MPP.Methods:Sixty children diagnosed as MPP in our hospital between July 2013 and December 2013 were included,and another 60 healthy children undergoing the physical examination at the out-patient in the corresponding period were recruited as controls.The peripheral blood was ob-tained from the two groups and measured for the levels of T lymphocyte subsets.Results:The levels of CD3^+,CD4^+,CD8^+and CD4^+/CD8^+were 69.12 &#177;8.07,37.76 ±8.22,27.96 ±9.28 and 1.53 ±0.56,respectively,for the in MPP group,whose CD3^+,CD4^ +and CD4 +/CD8^+levels were signifi-cantly decreased,yet CD8 +level was markedly elevated as compared with the controls(P〈0.01).Conclusion:Imbalanced T lymphocyte subsets were found in children with MPP,which suggests that cellular immune dysfunction may play an important role in the pathogenesis of mycoplasma pneumoniae pneumonia.
Keywords:mycoplasma pneumoniae pneumonia  T lymphocyte subsets  cellular immunity
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