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新疆地区耐多药与药物敏感肺结核患者外周血转录组学差异及免疫浸润特征分析

徐亮亮 刘欣 杨婷 张君 陈志祥 关小军 郑甜

新发传染病电子杂志2026,Vol.11Issue(1):23-27,5.
新发传染病电子杂志2026,Vol.11Issue(1):23-27,5.DOI:10.19871/j.cnki.xfcrbzz.2026.01.003

新疆地区耐多药与药物敏感肺结核患者外周血转录组学差异及免疫浸润特征分析

Transcriptomic differences and immune infiltration characteristics in peripheral blood of multidrug-resistant and drug-sensitive pulmonary tuberculosis patients in Xinjiang

徐亮亮 1刘欣 2杨婷 3张君 4陈志祥 5关小军 1郑甜6

作者信息

  • 1. 新疆维吾尔自治区第六人民医院胸外一科,新疆 乌鲁木齐 830013
  • 2. 新疆维吾尔自治区第六人民医院临床营养科,新疆 乌鲁木齐 830013
  • 3. 新疆维吾尔自治区第六人民医院检验科,新疆 乌鲁木齐 830013
  • 4. 新疆维吾尔自治区第六人民医院结核二科,新疆 乌鲁木齐 830013
  • 5. 新疆维吾尔自治区第六人民医院胸外二科,新疆 乌鲁木齐 830013
  • 6. 新疆维吾尔自治区第六人民医院教科办,新疆 乌鲁木齐 830013
  • 折叠

摘要

Abstract

Objective To analyze the differences in peripheral blood transcriptomics and immune infiltration characteristics between multidrug-resistant tuberculosis(MDR-TB)and drug-susceptible tuberculosis(DS-TB)patients,explore the correlation between differential gene expression levels and immune cell proportions,and provide evidence for elucidating the pathogenesis of MDR-TB.Method This cross-sectional study enrolled 10 pulmonary tuberculosis patients who admitted to Sixth People's Hospital of Xinjiang Uygur Autonomous Region from January to December 2024.Based on molecular drug sensitivity results,they were divided into a multidrug-resistant group and a drug-sensitive group.Venous whole blood samples were collected from each patients,and RNA was extracted for high-throughput sequencing.Differentially expressed genes in the two groups were identified through mRNA transcriptomics analysis.The gene ontology(GO)and Kyoto encyclopedia of genes and genomes(KEGG)databases were used to perform functional annotation and pathway enrichment analysis on the differentially expressed genes to clarify their associated functions and core enriched pathways.The immune cell composition of the patients was calculated using the quantexq algorithm,and the differences in immune cell percentage between the two groups were compared.Immune-related differentially expressed genes were selected,and Spearman correlation analysis was used to calculate the correlation between these genes and the immune cell percentages.Result Using drug-sensitive pulmonary tuberculosis patients as the control and based on the predefined screening thresholds for differentially expressed genes,a total of 583 differentially expressed genes were identified in multidrug-resistant pulmonary tuberculosis patients,including 330 upregulated genes and 253 downregulated genes.Among the 10 immune cell types,the percentage of neutrophils in multidrug-resistant group was significantly higher than that in drug-sensitive tuberculosis group(P<0.05).The expression levels of seven immune-related differentially expressed genes showed a strong correlation with the percentage of neutrophils(|R|>0.5),with MAP1LC3A and CASP5 showing the strongest correlation.Specifically,the expression level of MAP1LC3A was negatively correlated with the proportion of neutrophils(R=-0.527,P=0.117),while the expression level of CASP5 was positively correlated with the proportion of neutrophils(R=0.661,P=0.038).Conclusion Compared with drug-sensitive patients,multidrug-resistant tuberculosis patients had a significantly increased percentage of peripheral blood neutrophils.Downregulation of MAP1LC3A and upregulation of CASP5 in the peripheral blood of multidrug-resistant tuberculosis patients were highly correlated with the increased percentage of neutrophils.The autophagy mechanism mediated by MAP1LC3A and the abnormal neutrophil extracellular traps generation and inflammatory response mainly based on CASP5 were important breakthroughs for in-depth research into the drug resistance mechanism of pulmonary tuberculosis.

关键词

肺结核/耐多药/转录组测序/免疫微环境

Key words

Pulmonary tuberculosis/Multidrug-resistant/Transcriptomics/Immune microenvironment

分类

医药卫生

引用本文复制引用

徐亮亮,刘欣,杨婷,张君,陈志祥,关小军,郑甜..新疆地区耐多药与药物敏感肺结核患者外周血转录组学差异及免疫浸润特征分析[J].新发传染病电子杂志,2026,11(1):23-27,5.

基金项目

1.省部共建中亚高发病成因与防治国家重点实验室联合基金项目(SKL-HIDCA-2024-BF5)2.新疆维吾尔自治区第六人民医院2020年度院级科研项目(202004) (SKL-HIDCA-2024-BF5)

新发传染病电子杂志

2096-2738

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