免疫系统
白细胞介素2受体
CD8型
FOXP3型
免疫学
细胞毒性T细胞
细胞因子
生物
T细胞
体外
生物化学
作者
Agnieszka Jasiecka-Mikołajczyk,Jerzy Jan Jaroszewski,Tomasz Maślanka
出处
期刊:Polish Journal of Veterinary Sciences
[De Gruyter]
日期:2018-12-01
卷期号:21 (4): 819-822
标识
DOI:10.24425/pjvs.2018.125994
摘要
Due to the unrecognized effect of tigecycline (TIG) on CD4+ and CD8+ T cells, the present study has been undertaken in order to determine whether the drug can affect these cells in respect of their counts, and the production of IFN-γ, IL-17 (pro-inflammatory and immune-protective cytokines), IL-4 (anti-inflammatory and immune-protective cytokine), IL-10 and TGF-β (anti-inflammatory and immune-suppressive cytokines). Murine lymphocytes were treated with TIG for 48 and 96 h at concentrations reflecting its plasma levels obtained in vivo at therapeutic doses, and at 10-fold lower concentrations. It was found that TIG neither affected substantially the percentage and absolute counts of entire CD4+ and CD8+ T cell populations nor influenced the Foxp3+CD25+CD4+ regulatory/suppressive T cell subset. Furthermore, the percentages of IL-4-, IL-10-, IL-17- and TGF-β-producing CD4+ T cells were not altered following the exposure to TIG. Similarly, TIG did not influence IFN-γ production by CD8+ T cells. Thus, with respect to the parameters evaluated, TIG does not seem to exert immune-suppressive and anti-inflammatory effects.
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