Inflammation regulating cytokines in TB affected tissues
Galina S. Shepelkova, Vladimir Evstifeev, Ruslan V. Tarasov, Mamed A. Bagirov, Vladimir Yeremeev
Abstract
Galina S. Shepelkova, Vladimir Evstifeev, Ruslan V. Tarasov, Mamed A. Bagirov, Vladimir Yeremeev
Abstract
Introduction: Cytokines play important role in regulating infection without promoting uncontrolled and damaging inflammatory responses. Herein we focus on the key cytokines and chemokines expressed at the site of infection – in the lungs of TB patients. Aims and objectives: We compared the levels of cytokine/chemokine gene expression in the tuberculoma/caverna wall and in relatively intact tissue at the periphery of resected specimen from post-primary TB patients. Methods: Written informed consent was obtained from each participant prior to biopsy collection. The expression levels of cytokines/chemokines genes were analyzed by TaqMan PCR Assay. ELISA was used to estimate respective proteins in tissue homogenates. Results: Most prominent differences in cytokine/chemokine genes expression were registered when FCT cavity wall and parenchyma tissues were compared. Cxcl1 (p ≤ 0.03) and Cxcl2 (p ≤ 0.01), IL6 (p≤0.0001), IL8 (p ≤0.01) were upregulated in parenchymatous tissue as compared to cavity wall. Destruction processes in tuberculoma patients correlate with the levels of cell migration factors such as IL-6, G-CSF and MIP-1a. Conclusions: Our data indicate significant changes in the levels of certain cytokines/chemokines in the lungs of patients with post-primary TB. These changes primarily concern cytokines/chemokines involved in the regulation of specific inflammation, cell migration and fibrosis formation. This work was supported by the Scientific Program SR 0515-2019-0018.
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Introduction: Cytokines play important role in regulating infection without promoting uncontrolled and damaging inflammatory responses. Herein we focus on the key cytokines and chemokines expressed at the site of infection – in the lungs of TB patients. Aims and objectives: We compared the levels of cytokine/chemokine gene expression in the tuberculoma/caverna wall and in relatively intact tissue at the periphery of resected specimen from post-primary TB patients. Methods: Written informed consent was obtained from each participant prior to biopsy collection. The expression levels of cytokines/chemokines genes were analyzed by TaqMan PCR Assay. ELISA was used to estimate respective proteins in tissue homogenates. Results: Most prominent differences in cytokine/chemokine genes expression were registered when FCT cavity wall and parenchyma tissues were compared. Cxcl1 (p ≤ 0.03) and Cxcl2 (p ≤ 0.01), IL6 (p≤0.0001), IL8 (p ≤0.01) were upregulated in parenchymatous tissue as compared to cavity wall. Destruction processes in tuberculoma patients correlate with the levels of cell migration factors such as IL-6, G-CSF and MIP-1a. Conclusions: Our data indicate significant changes in the levels of certain cytokines/chemokines in the lungs of patients with post-primary TB. These changes primarily concern cytokines/chemokines involved in the regulation of specific inflammation, cell migration and fibrosis formation. This work was supported by the Scientific Program SR 0515-2019-0018.
Key concepts: Chemokine, CXCL1, CXCL2, Medicine, Cytokine, Inflammation, Tuberculoma, CCL3