周杰林, 徐婷, 许如菊, 林先耀. 胸腺活化调节趋化因子在儿童肺炎支原体感染致哮喘发作中的作用[J]. 疾病监测, 2016, 31(1): 45-48. DOI: 10.3784/j.issn.1003-9961.2016.01.011
引用本文: 周杰林, 徐婷, 许如菊, 林先耀. 胸腺活化调节趋化因子在儿童肺炎支原体感染致哮喘发作中的作用[J]. 疾病监测, 2016, 31(1): 45-48. DOI: 10.3784/j.issn.1003-9961.2016.01.011
ZHOU Jie-lin, XU Ting, XU Ru-ju, LIN Xian-yao. Role of thymus activation regulated chemokine in Mycoplasma pneumoniae caused asthma in children[J]. Disease Surveillance, 2016, 31(1): 45-48. DOI: 10.3784/j.issn.1003-9961.2016.01.011
Citation: ZHOU Jie-lin, XU Ting, XU Ru-ju, LIN Xian-yao. Role of thymus activation regulated chemokine in Mycoplasma pneumoniae caused asthma in children[J]. Disease Surveillance, 2016, 31(1): 45-48. DOI: 10.3784/j.issn.1003-9961.2016.01.011

胸腺活化调节趋化因子在儿童肺炎支原体感染致哮喘发作中的作用

Role of thymus activation regulated chemokine in Mycoplasma pneumoniae caused asthma in children

  • 摘要: 目的 研究胸腺活化调节趋化因子(TARC)在儿童肺炎支原体(MP)感染致哮喘发作中的作用。方法 收集肺炎患儿73例(支气管哮喘患儿除外)。在入院时(急性期)采集静脉血用被动凝集法检测MP-IgM并用间接免疫荧光法检测其他7种呼吸病原体IgM, 并于-70 ℃保存部分血清;采集咽拭子用荧光定量-聚合酶链反应检测MP-DNA。根据临床诊断和MP-IgM或MP-DNA拷贝数分为MP感染组和非MP感染组。在病情明显好转时(恢复期), 对伴有哮喘发作的患儿采静脉血分离血清, 置于-70 ℃保存。采用酶联免疫吸附试验测定患儿血清中TARC的水平。评价血清中TARC水平在两组患儿之间以及急性期和恢复期之间的差异性。结果 MP感染组患儿中有哮喘发作的比例高于非MP感染组, 差异有统计学意义(2=4.44, P=0.04)。MP感染组患儿的TARC水平高于非感染组, 差异有统计学意义(t=4.01, P=0.00)。MP感染组, 有哮喘发作患儿的TARC水平高于非MP感染组有哮喘发作患儿和无哮喘发作患儿, 差异有统计学意义(t=2.62, P=0.01;t=5.21, P=0.00);TARC水平无哮喘发作患儿的高于非MP感染组无哮喘发作患儿, 差异有统计学意义(t=2.07, P=0.05)。MP感染组和非MP感染组, 有哮喘发作患儿的TARC水平均高于无哮喘发作患儿, 差异有统计学意义(t=2.11, P=0.04;t=2.03, P=0.05);有哮喘发作患儿恢复期的TARC水平较急性期均有下降, 差异有统计学意义(t=4.69, P=0.00;t=2.37, P=0.05)。结论 TARC在MP感染诱发哮喘发作中起重要作用。

     

    Abstract: Objective To study the role of thymus activation regulated chemokine (TARC) in Mycoplasma pneumoniae caused asthma in children. Methods Seventy three children with acute pneumonia were included in this study (excluding the children with bronchial asthma). At the time of admission, venous blood samples were collected from the children to detect MP-IgM with passive hemagglutination method and IgM antibodies of other 7 respiratory pathogens with indirect immunofluorescence (IIF). A part of the serum was stored at -70 ℃. Throat swabs were collected to detect MP-DNA with quantitative RT-PCR. According to the clinical diagnosis of Mycoplasma pneumoniae infection and serum MP-IgM or MP-DNA copy number of induced sputum, the children with pneumonia were divided into MP infection group and non MP infection group. In convalescence phase, the venous blood samples were collected from the children with asthma attack; and the serum was stored at -70 ℃. The level of TARC in serum was detected with enzyme linked immunosorbent assay (ELISA). The differences in serum TARC level between the MP infection group and non MP infection group and between acute phase and convalescence phase were analyzed. Results The attack rate of asthma was higher in MP infection group than in non MP infection group, the difference had no statistical significance (2=4.44, P=0.04). The level of TARC was higher in MP infection group than in non MP infection group, the difference had statistical significance (t=4.01, P=0.00). In MP infection group, the children with asthma had higher level of TARC than those with and without asthma in non MP infection group, the differences had statistical significance (t=2.62, P=0.01; t=5.21, P=0.00), and the children without asthma had higher level of TARC than those without asthma in non MP infection group, the difference was statistical significant (t=2.07, P=0.05). In both MP infection group and non MP infection group, the levels of TARC in children with asthma were higher than those in children without asthma, the difference was statistical significant (t=2.11, P=0.04; t=2.03, P=0.05).The level of TARC in children with asthma in convalescence phase was lower than that in those in acute phase, the difference was statistical significant (t=4.69, P=0.00; t=2.37, P=0.05). Conclusion TARC plays an important role in the onset of MP infection induced asthma.

     

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