Çavuşoğlu Cengiz, Çoğulu Özgür, Durmaz Asude, Cengisiz Zehra, Yılmaz Fethiye Ferda, Taşbakan Mehmet Sezai, Taşbakan Meltem, Gündüz Cumhur, Biçmen Can, Karaman Onur, Taşlıdere Hasan, Akın Haluk, Akarca Tülay, Dereli Şevket
Department of Medical Microbiology, Faculty of Medicine, Ege University, İzmir, Turkey.
Department of Pediatrics, Faculty of Medicine, Ege University, İzmir, Turkey.
Turk J Med Sci. 2022 Jun;52(3):649-657. doi: 10.55730/1300-0144.5357. Epub 2022 Jun 16.
In tuberculsosis (TB), miRNA has been used as a biomarker to distinguish between healthy individuals and TB patients. The aim of this study was to investigate (i) the association of the miRNA and cytokine expression levels, the course of tuberculosis infection, clinical forms and response to treatment, and (ii) the effects of genotypic features of bacteria on the course of tuberculosis and the relationship between miRNA and cytokine expressions and bacterial genotypes.
A total of 200 cases (100: culture positive active tuberculosis, 50: quantiferon positive latent tuberculosis infection and 50: quantiferon negative healthy controls) were included in the study. For the tuberculosis group at the time of admission and after treatment, for the latent tuberculosis infection and healthy control groups at the time of admission, miRNA and cytokine expressions were determined. Genotyping of M.tuberculosis isolates was performed by spoligotyping method.
While, in the comparison of miRNA expressions between the pretreatment patient group and the healthy control group, there was a statistically significant decrease in the expression of miR-454-3p, miR-15a-5p, miR-590-5p, miR-381, and miR-449a in the Pulmonary TB group, there was no significant change in miRNA expression in extrapulmonary TB patients. When the cytokine expressions of the patient group and the healthy control group were compared before treatment, the expressions of all cytokines in the patient group decreased. However, the only cytokine that showed a significantly lower expression was IL12A in PTB patients.
There is no significant relationship between the clinical course of the disease, cytokine and miRNA expression, and the genotype of the bacteria.
在结核病(TB)中,微小RNA(miRNA)已被用作区分健康个体和结核病患者的生物标志物。本研究的目的是调查(i)miRNA与细胞因子表达水平、结核感染病程、临床类型及治疗反应之间的关联,以及(ii)细菌基因型特征对结核病病程的影响,以及miRNA与细胞因子表达和细菌基因型之间的关系。
本研究共纳入200例患者(100例:培养阳性的活动性肺结核,50例:结核菌素试验阳性的潜伏性结核感染,50例:结核菌素试验阴性的健康对照)。对结核病组入院时及治疗后、潜伏性结核感染组和健康对照组入院时的miRNA和细胞因子表达进行了测定。采用间隔寡核苷酸分型法对结核分枝杆菌分离株进行基因分型。
在预处理患者组与健康对照组之间的miRNA表达比较中,肺结核组中miR-454-3p、miR-15a-5p、miR-590-5p、miR-381和miR-449a的表达有统计学意义的下降,而肺外结核患者的miRNA表达无显著变化。治疗前患者组与健康对照组的细胞因子表达比较中,患者组所有细胞因子的表达均下降。然而,在肺结核患者中,唯一表达显著降低的细胞因子是IL12A。
疾病的临床病程、细胞因子和miRNA表达与细菌基因型之间无显著关系。