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作 者:郭赟[1] 钱俊[1] 李羚[1] 惠郁[1] 蒋汉民[1]
机构地区:[1]南京医科大学附属无锡人民医院儿童医院呼吸科,214023
出 处:《国际儿科学杂志》2016年第8期647-650,共4页International Journal of Pediatrics
摘 要:目的探讨CD4^+CD25^+FoxP3^+Treg细胞在儿童重症肺炎支原体肺炎(severe mycoplasma pneumoniae pneumonia, SMPP)中的作用。方法采用流式细胞仪检测65例重症肺炎支原体肺炎患儿(SMPP组)、75例非重症肺炎支原体肺炎患儿(Non—SMPP组)及40例健康儿童(健康对照组)急性期及恢复期外周血CD4^+CD25^+FoxP3^+Treg细胞占CD4^+T细胞的比例并进行比较分析。结果急性期SMPP组CD4^+CD25^+FoxP3^+Treg表达低于Non—SMPP组(0.87±0.66%vs.1.17±0.70%,P〈0.05)及对照组(0.87±0.66%vs.3.88±2.00%,P〈0.01)。Non—SMPP组CD4^+CD25^+FoxP3^+Treg表达低于对照组(I.17±0.70%VS.3.88±2.00%,P〈0.01)。恢复期SMPP组CD4^+CD25^+FoxP3^+淋巴细胞比例较Non-SMPP组降低(1.66±0.85%vs.3.61±1.45%,P〈0.01)。恢复期SMPP组CD4^+CD25^+FoxP3^+淋巴细胞比例较急性期升高(1.66±0.85%vs.0.87±0.66%,P〈0.01),恢复期Non—SMPP组CD4^+CD25^+FoxP3^+淋巴细胞比例较急性期亦升高(3.61±1.45%VS.1.17±0.70%,P〈0.01)。结论CD4^+CD25^+FoxP3^+Treg在SMPP的发病中起一定作用,低表达CD4^+CD25^+FoxP3^+Treg的患儿可能在感染MP后患SMPP的易患性增加,同时影响SMPP患儿预后。Objective To investigate the role of CD4^+CD25^+FoxP3^+ in severe Mycoplasma pneumonia among children. Methods One hundred and forty children with M. pneumoniae pneumonia (65 severe and 75 non-severe) who were hospitalized were enrolled along with forty other children as controls. X-ray was assessed. The proportions of peripheral blood CD4^+CD25^+FoxP3^+ cells were determined by flow cytometry. Results Both severe and non-severe children had decreased CD4^+CD25^+FoxP3^+ cells as compared with control subjects in acute phase (0.87±0.66% vs. 3.88 ±2.00%, P〈0.01 and 1.17 ±0.70% vs. 3.88 ± 2. 00%, P 〈0. 01, respectively). The levels of CD4^+CD25^+FoxP3^+ cells in severe children were lower than those in non-severe children in acute phase and recovery phase (0. 87± 0. 66% vs. 1.17 ± 0.70%, P 〈 0. 05 and 1.66±0. 85% vs. 3.61± 1.45%, P 〈0. 01, respectively) . Both severe children and non-severe children expressed higher CD4^+CD25^+FoxP3^+ cells in recovery phase than in acute phase ( 1.66 ± 0. 85% vs. 0. 87± 0.66%, P〈0.01 and 3.61±1.45% vs. 1.17±0.70%, P〈0.01, respectively). Conclusion The expression of CD4^+CD25^+FoxP3^+ Tregs may play a role in the onset of severity of mycoplasma pneumonia and the low express of CD4^+CD25^+FoxP3^+ Tregs in children infected with M. pneumonia may increase the susceptibility to severe mycoplasma pneumonia.
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