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细菌溶解产物胶囊联合益生菌对过敏性哮喘患儿Notch信号通路指标、肠道菌群及临床疗效的影响
Effects of bacterial lysate capsules combined with probiotics on Notch signaling pathway indicators, intestinal microbiota, and clinical efficacy in children with allergic asthma

内科 页码:274-279

作者机构:河南省漯河市中心医院儿科,漯河市 462000

DOI:10.16121/j.cnki.cn45-1347/r.2025.03.09

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目的 探讨细菌溶解产物胶囊联合益生菌对过敏性哮喘(AA)患儿Notch信号通路指标、肠道菌群及临床疗效的影响。方法 选取99例AA患儿作为研究对象,随机将其分为泛福舒组、益生菌组、联合组,每组33例。在抗炎、平喘等常规治疗基础上,三组分别采用细菌溶解产物胶囊、双歧杆菌四联活菌片、细菌溶解产物胶囊联合双歧杆菌四联活菌片治疗,三组均持续治疗3个月。比较三组治疗前后的Notch信号通路指标、免疫学指标[γ-干扰素(IFN-γ)、白细胞介素-4(IL-4)、总免疫球蛋白E(tIgE)]、肠道菌群菌落数、哮喘症状评分,治疗3个月后的哮喘控制水平,以及治疗期间不良反应发生情况。结果 治疗前,三组基线指标差异均无统计学意义(均P>0.05)。治疗1个月及3个月后,三组NOTCH1 mRNA、NOTCH4 mRNA相对表达量,血清IL-4、tIgE水平,以及日间、夜间症状评分均呈联合组<泛福舒组<益生菌组(均P<0.05);血清IFN-γ水平均呈联合组>泛福舒组>益生菌组(均P<0.05)。治疗3个月后,三组哮喘控制总有效率整体差异有统计学意义(P<0.05),且联合组哮喘控制总有效率高于益生菌组(P<0.05);三组肠道双歧杆菌、乳杆菌菌落数均呈联合组>益生菌组>泛福舒组(均P<0.05)。三组治疗期间不良反应总发生率差异无统计学意义(P>0.05)。结论 细菌溶解产物胶囊联合益生菌治疗儿童AA较单药治疗更具优势,其机制可能通过协同下调Notch信号通路活性、纠正Th1/Th2免疫失衡及改善肠道菌群定植实现,在显著提高临床疗效的同时未增加不良反应发生率。

Objective To explore the effects of bacterial lysate capsules combined with probiotics on Notch signaling pathway indicators, intestinal microbiota, and clinical efficacy in children with allergic asthma (AA). Methods A total of 99 children with AA were selected as research subjects and randomly divided into the Broncho-Vaxom group, probiotic group, or combined group, with 33 cases in each group. On the basis of conventional anti-inflammatory and anti-asthmatic therapies, the three groups were treated with bacterial lysate capsules, Bifidobacterium quadruple live tablets, and bacterial lysate capsules combined with Bifidobacterium quadruple live tablets, respectively, all for 3 consecutive months. The Notch signaling pathway indicators, immunological indicators (interferon-γ [IFN-γ], interleukin-4 [IL-4], and total immunoglobulin E [tIgE]), counts of intestinal microbiota colonies, and asthma symptom score before and after treatment; the asthma control level after 3 months of treatment; and incidence of adverse reactions during treatment were compared among the three groups. Results Before treatment, there was no statistically significant difference in the baseline indicators among the three groups (all P>0.05). At 1 month and 3 months after treatment initiation, the relative expression levels of NOTCH1 mRNA and NOTCH4 mRNA, serum levels of IL-4 and tIgE, and daytime and nighttime symptom scores in the three groups showed a trend of the combined group's < the Broncho-Vaxom group's < the probiotic group's (all P<0.05); the serum IFN-γ level in the three groups showed a trend of the combined group's > the Broncho-Vaxom group's > the probiotic group's (all P<0.05). At 3 months after treatment initiation, there was a statistically significant overall difference in the total effective rate of asthma control among the three groups (P<0.05), and the total effective rate of asthma control in the combined group was higher than that in the probiotic group (P<0.05); the counts of intestinal Bifidobacteria and Lactobacilli in the three groups showed a trend of the combined group's > the probiotic group's > the Broncho-Vaxom group's (all P<0.05). There was no statistically significant difference in the total incidence of adverse reactions among the three groups during treatment (P>0.05). Conclusion The combined use of bacterial lysate capsules and probiotics demonstrates superior efficacy over monotherapy in treating pediatric AA, potentially mediated by synergistic downregulation of Notch signaling pathway activity, correction of Th1/Th2 immune imbalance, and improvement in gut microbiota colonization, significantly enhancing clinical outcomes without increasing adverse reactions.

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