Altered NCF2, NOX2 mRNA Expression Levels in Peripheral Blood Mononuclear Cells of Pulmonary Tuberculosis Patients

被引:10
作者
Li, Hong-Miao [1 ,2 ]
Huang, Qian [1 ]
Tang, Fen [2 ]
Zhang, Tian-Ping [3 ]
机构
[1] Anhui Med Univ, Sch Publ Hlth, Dept Epidemiol & Biostat, Hefei 230032, Anhui, Peoples R China
[2] Anhui Chest Hosp, Anhui Prov TB Inst, Hefei 230022, Anhui, Peoples R China
[3] Univ Sci & Technol China, Affiliated Hosp 1, Div Life Sci & Med, Hefei 230001, Anhui, Peoples R China
来源
INTERNATIONAL JOURNAL OF GENERAL MEDICINE | 2021年 / 14卷
关键词
pulmonary tuberculosis; NADPH oxidase complex; NCF2; NOX2; peripheral blood mononuclear cells; CHRONIC GRANULOMATOUS-DISEASE; NADPH OXIDASE; MYCOBACTERIUM-TUBERCULOSIS; CYBB; SUSCEPTIBILITY;
D O I
10.2147/IJGM.S339194
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Reactive oxygen species (ROS) generated by NADPH oxidase has a pivotal role in the nonspecific innate immune response to invading microorganisms including M. tuberculosis (MTB). NCF2 and NOX2 were considered as important functional subunits of NADPH oxidase complex; hence, this study aimed to evaluate the NCF2, NOX2 mRNA expressions in PBMC of pulmonary tuberculosis (PTB) patients. Methods: A total of 79 PTB patients and 73 controls were included in our study. Quantitative real-time reverse transcription polymerase chain reaction (qRT-PCR) was used to measure the NCF2, NOX2 mRNA levels, and receiver operating characteristic (ROC) curve analysis was performed to assess the diagnostic value of NCF2, NOX2 in PTB patients. Results: When compared to controls, the NCF2, NOX2 mRNA levels were significantly increased in PBMC from PTB patients (P < 0.001). However, the NCF2, NOX2 mRNA levels were not associated with major clinical and laboratory data of PTB patients. Area under curve (AUC) of ROC curve analysis for NCF2 and NOX2 were 0.686 (95% CI: 0.601, 0.770) and 0.705 (95% CI: 0.623, 0.787), respectively. Conclusion: Altered NCF2, NOX2 mRNA levels in PTB patients implied that these genes might play roles in PTB, and their expression levels might be potential biomarkers for the diagnosis of PTB.
引用
收藏
页码:9203 / 9209
页数:7
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