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Study on the Correlation between Interleukin-27 and CXCL10 in Pulmonary Tuberculosis

OBJECTIVE: To investigate the correlation between interleukin-27 and CXCL10 and other cytokines in pulmonary tuberculosis and to further explore the related miRNAs through bioinformatics. METHODS: Collect the lesion tissue and peripheral blood of pulmonary tuberculosis patients and the peripheral bl...

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Detalles Bibliográficos
Autores principales: Fan, Jiahui, Yang, Yefeng, Wang, Liang, Shang, Xiaoqian, Zhang, Li, Sun, Hu, Ma, Yujie, Li, Ying, Wang, Jing, Ma, Xiumin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9242752/
https://www.ncbi.nlm.nih.gov/pubmed/35785034
http://dx.doi.org/10.1155/2022/2932837
Descripción
Sumario:OBJECTIVE: To investigate the correlation between interleukin-27 and CXCL10 and other cytokines in pulmonary tuberculosis and to further explore the related miRNAs through bioinformatics. METHODS: Collect the lesion tissue and peripheral blood of pulmonary tuberculosis patients and the peripheral blood of healthy controls. Immunohistochemical staining and qRT-PCR were used to observe the expression of interleukin-27, CXCL9, CXCL10, and CXCL11. Then, predict the key miRNA, qRT-PCR was used to verify the expression of miRNA in the peripheral blood and evaluated the correlation between them. RESULTS: Both immunohistochemical staining and qRT-PCR indicated that the expressions of IL-27, CXCL9, CXCL10, and CXCL11 were significantly increased in tuberculosis patients, and IL-27 was significantly correlated with CXCL10 (r = 0.68). Key molecules such as has-let-7b-5p, has-miR-30a-3p, and has-miR-320b were screened out. Among them, has-let-7b-5p was significantly downregulated, and has-miR-30a-3p was significantly upregulated; they were related to interleukin-27 and CXCL10. CONCLUSION: Our data shows that interleukin-27 and CXCL10 are significantly related in pulmonary tuberculosis, and has-let-7b-5p and has-miR-30a-3p are also related to interleukin-27 and CXCL10. It laid the foundation for subsequently exploiting the potential biomarkers in tuberculosis disease.