Effect of heat shock factor 1 on airway hyperresponsiveness and airway inflammation in mice with allergic asthma / 中国当代儿科杂志

<p><b>OBJECTIVE</b>To investigate the effect of heat shock factor 1 (HSF1) on airway hyperresponsiveness and airway inflammation in mice with asthma and possible mechanisms.</p><p><b>METHODS</b>A total of 36 mice were randomly divided into four groups: control, asthma, HSF1 small interfering RNA negative control (siHSF1-NC), and siHSF1 intervention (n=9 each). Ovalbumin (OVA) sensitization and challenge were performed to induce asthma in the latter three groups. The mice in the siHSF1-NC and siHSF1 groups were treated with siHSF1-NC and siHSF1, respectively. A spirometer was used to measure airway responsiveness at 24 hours after the last challenge. The direct count method was used to calculate the number of eosinophils. ELISA was used to measure the serum level of OVA-specific IgE and levels of interleukin-4 (IL-4), interleukin-5 (IL-5), interleukin-13 (IL-13), and interferon-γ (IFN-γ) in lung tissues and bronchoalveolar lavage fluid (BALF). Quantitative real-time PCR was used to measure the mRNA expression of HSF1 in asthmatic mice. Western blot was used to measure the protein expression of HSF1, high-mobility group box 1 (HMGB1), and phosphorylated c-Jun N-terminal kinase (p-JNK).</p><p><b>RESULTS</b>The asthma group had significant increases in the mRNA and protein expression of HSF1 compared with the control group (P<0.05). The siHSF1 group had significantly reduced mRNA and protein expression of HSF1 compared with the siHSF1-NC group (P<0.05). The knockdown of HSF1 increased airway wall thickness, airway hyperresponsiveness, OVA-specific IgE content, and the number of eosinophils (P<0.05). Compared with the siHSF1-NC group, the siHSF1 group had significantly increased levels of IL-4, IL-5, and IL-13 and significantly reduced expression of IFN-γ in lung tissues and BALF (P<0.05), as well as significantly increased expression of HMGB1 and p-JNK (P<0.05).</p><p><b>CONCLUSIONS</b>Knockdown of HSF1 aggravates airway hyperresponsiveness and airway inflammation in asthmatic mice, and its possible mechanism may involve the negative regulation of HMGB1 and JNK.</p>

Effect of Mycoplasma pneumoniae infection on function of T lymphocytes in bronchoalveolar lavage fluid of asthmatic children / 中国当代儿科杂志

<p><b>OBJECTIVE</b>To investigate the effect of Mycoplasma pneumoniae (MP) infection on the function of T lymphocytes in the bronchoalveolar lavage fluid (BALF) of asthmatic children in acute and stable periods and the relationship between MP infection and asthma.</p><p><b>METHODS</b>Seventy-one hospitalized children (with bronchitis, pneumonia, and asthma) were divided into non-MP infection control group (group A, pneumonia and bronchitis without MP infection), non-MP infection asthma group (group B), and MP infection asthma group (group C). Flow cytometry was used to determine CD3(+), CD4(+), and CD8(+) T cell counts and CD4(+)/CD8(+) ratio in BALF among all children in acute and stable periods.</p><p><b>RESULTS</b>Compared with group A, groups B and C showed significant differences in CD3(+), CD4(+), and CD8(+) T cell counts and CD4(+)/CD8(+) ratio (P<0.05) in acute and stable periods, had decreased CD3(+) and CD4(+) T cell counts, an increased CD8(+) T cell count, and a significantly decreased CD4(+)/CD8(+) ratio (P<0.05) in the acute period, and had decreased CD3(+) and CD4(+) T cell counts and CD4(+)/CD8(+) ratio and an increased CD8(+) T cell count (P<0.05) in the stable period. Compared with group B, group C had significantly decreased CD3(+) and CD4(+) T cell counts and CD4(+)/CD8(+) ratio (P<0.05) and a significantly increased CD8(+) T cell count (P<0.05) in the acute period and showed no significant differences in CD3(+), CD4(+), and CD8(+) T cell counts (P>0.05) and a significant decrease in CD4(+)/CD8(+) ratio (P<0.05) in the stable period.</p><p><b>CONCLUSIONS</b>The immunological function of T lymphocytes in the airway declines significantly among asthmatic children with MP infection in acute and stable periods, leading to immue system disorder. MP may be associated with the pathogenesis of asthma.</p>