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阻塞性睡眠呼吸暂停患者的血液细胞因子、CD4 T 细胞、NK 和中性粒细胞改变。

Altered blood cytokines, CD4 T cells, NK and neutrophils in patients with obstructive sleep apnea.

机构信息

Department of Microbiology and Immunology, College of Medicine and Health Sciences, Sultan Qaboos University, P.O. Box: 35, 123, Muscat, Oman.

Department of Clinical Physiology, Sultan Qaboos University Hospital, P.O. Box: 38, 123, Muscat, Oman.

出版信息

Immunol Lett. 2017 Oct;190:272-278. doi: 10.1016/j.imlet.2017.08.009. Epub 2017 Aug 19.

Abstract

BACKGROUND

There are contradictory reports on the effects of obstructive sleep apnea (OSA) on the immune system. In order to clarify the effect of OSA on the different components of the immune system, we studied the association of OSA with changes in cytokine and chemokine levels, proliferative patterns of CD4 and CD8 T lymphocytes as well as NK cells ex vivo and neutrophil functions.

METHODS

We investigated the association of OSA with potential alterations in 14 Th1/Th2 and inflammatory cytokines and chemokines, CD4 and CD8 T cells, NK cells, and the NADPH oxidase activation and phagocytic functions in neutrophils.

RESULTS

Our results suggest that the increase in CD4 T cell frequency in OSA is associated with an increased expression of the nuclear protein Ki67 (p<0.05; power>0.8), and is correlated with the levels of IL-1β (p<0.05; power>0.8). The levels of IL-1β as well as IL-6 showed a potential increase, while the levels of IFN-γ (p<0.05; power>0.8) and the ratio IFN-γ/IL-4 in the blood were possibly decreased in OSA. Additionally, we observed a potential increase in the expression of Ki67 in CD8 and CD8 NK cells (p<0.05; power>0.8). Our results also suggest that neutrophils have a decreased capacity to phagocytose bacteria and activate NADPH oxidase in OSA patients (p<0.05; power>0.8).

CONCLUSION

OSA may be associated with inflammatory and pro-Th2 immune responses, an increased proliferative potential of NK and CD4 T cells and a decreased capacity of neutrophils to phagocytose bacteria and produce ROS.

摘要

背景

阻塞性睡眠呼吸暂停(OSA)对免疫系统的影响存在相互矛盾的报道。为了阐明 OSA 对免疫系统不同成分的影响,我们研究了 OSA 与细胞因子和趋化因子水平变化、CD4 和 CD8 T 淋巴细胞以及 NK 细胞的体外增殖模式以及中性粒细胞功能的关系。

方法

我们研究了 OSA 与潜在改变的 14 种 Th1/Th2 和炎症细胞因子和趋化因子、CD4 和 CD8 T 细胞、NK 细胞以及中性粒细胞 NADPH 氧化酶激活和吞噬功能之间的关联。

结果

我们的结果表明,OSA 中 CD4 T 细胞频率的增加与核蛋白 Ki67 的表达增加相关(p<0.05;功效>0.8),并与 IL-1β 水平相关(p<0.05;功效>0.8)。IL-1β 以及 IL-6 水平可能增加,而 IFN-γ 水平(p<0.05;功效>0.8)和血液中 IFN-γ/IL-4 比值可能降低。此外,我们观察到 CD8 和 CD8 NK 细胞中 Ki67 的表达可能增加(p<0.05;功效>0.8)。我们的研究结果还表明,OSA 患者的中性粒细胞吞噬细菌和激活 NADPH 氧化酶的能力降低(p<0.05;功效>0.8)。

结论

OSA 可能与炎症和促 Th2 免疫反应、NK 和 CD4 T 细胞的增殖潜力增加以及中性粒细胞吞噬细菌和产生 ROS 的能力降低有关。

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