Wang Nan, Ma Qianqian, Zhang Junxian, Wang Jie, Li Xiaojun, Liang Yan, Wu Xueqiong
Tuberculosis Prevention and Control Key Laboratory, Beijing Key Laboratory of New Techniques of Tuberculosis Diagnosis and Treatment, Department of Tuberculosis, The Eighth Medical Center of PLA General Hospital, PLA General Hospital, Beijing, China.
Graduate School, Hebei North University, Zhangjiakou, Hebei, China.
Front Pharmacol. 2024 Sep 19;15:1415951. doi: 10.3389/fphar.2024.1415951. eCollection 2024.
Integrated traditional Chinese medicine and biomedicine is an effective method to treat tuberculosis (TB). In our previous research, traditional Chinese medicine preparation NiuBeiXiaoHe (NBXH) achieved obvious anti-TB effects in animal experiments and clinical practice. However, the action mechanism of NBXH has not been elucidated.
Peripheral blood mononuclear cells (PBMCs) were collected to extract mRNA and differentially expressed (DE) genes were obtained using gene microarray technology. Finally, GEO databases and RT-qPCR were used to verify the results of expression profile.
After MTB infection, most upregulated DE genes in mice were immune-related genes, including , , , , , and . Downregulated DE genes included , , , and . After treatment with NBXH, especially high-dose NBXH, the abnormal gene expression was significantly corrected. Some DE genes have been confirmed in multiple GEO datasets or in pulmonary TB patients through RT-qPCR.
MTB infection led to extensive changes in host gene expression and mainly caused the host's anti-TB immune responses. The treatment using high-dose NBXH partially repaired the abnormal gene expression, further enhanced the anti-TB immunity included autophagy and NK cell-mediated cytotoxicity, and had a certain inhibitory effect on overactivated immune responses.
中西医结合是治疗结核病的有效方法。在我们之前的研究中,中药制剂牛贝消核(NBXH)在动物实验和临床实践中均取得了明显的抗结核效果。然而,NBXH的作用机制尚未阐明。
采集外周血单个核细胞(PBMCs)提取mRNA,采用基因芯片技术获得差异表达(DE)基因。最后,利用GEO数据库和RT-qPCR验证表达谱结果。
结核分枝杆菌(MTB)感染后,小鼠中大多数上调的DE基因是免疫相关基因,包括 、 、 、 、 、和 。下调的DE基因包括 、 、 、和 。用NBXH治疗后,尤其是高剂量NBXH,异常基因表达得到显著纠正。一些DE基因已在多个GEO数据集中或通过RT-qPCR在肺结核患者中得到证实。
MTB感染导致宿主基因表达广泛变化,主要引发宿主的抗结核免疫反应。高剂量NBXH治疗部分修复了异常基因表达,进一步增强了包括自噬和NK细胞介导的细胞毒性在内的抗结核免疫力,并对过度激活的免疫反应有一定抑制作用。