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十七种炎症介质的调节与发热伴血小板减少综合征重症患者的预后相关。

The Regulation of Seventeen Inflammatory Mediators are Associated with Patient Outcomes in Severe Fever with Thrombocytopenia Syndrome.

机构信息

Department of Infectious Diseases, the First Affiliated Hospital of Anhui Medical University, Hefei, Anhui, China.

Department of Infectious Diseases, the Chaohu Affiliated Hospital of Anhui Medical University, Chaohu, Anhui, China.

出版信息

Sci Rep. 2018 Jan 9;8(1):159. doi: 10.1038/s41598-017-18616-z.

Abstract

Severe fever with thrombocytopenia syndrome (SFTS) as an emerging infection disease results in high morbidity and mortality in China. In this study, the circulating levels of 36 inflammatory mediators in 33 SFTS patients on days 3-7, 8-12 and 13-20 post-illness were measured by a multiplex Luminex® system dynamically. Among the patients, 15 severe patients recovered, 11 severe patients died within three weeks. We found IL-1RA, IL-6, IL-15, IL-10, TNF-α, IFN-γ, G-CSF, eotaxin, IL-8, IP-10, MCP-1, MIP-1α, MIP-1β and fractalkine were significantly upregulated in SFTS patients. Elevated IL-15 and eotaxin in SFTS patients were reported firstly. The highest levels of pro-inflammatory and anti-inflammatory cytokines coexisted in fatal patients during the first week. Inflammatory mediators remained high levels when death occurred in fatal patients, they were recovered within three weeks in nonfatal patients. Our results showed the occurrence of inflammatory storm in SFTS patients were associated with the severity of SFTS. RANTES and PDGF were down regulated and remained significantly lower levels in fatal patients throughout the course of disease, the concentrations of RANTES and PDGF were remarkably positively correlated with the platelet count. Our results demonstrated that dysregulated inflammatory response was associated with disease pathogenesis and mortality in SFTS patients.

摘要

严重发热伴血小板减少综合征(SFTS)是一种新发传染病,在中国发病率和死亡率均较高。本研究采用多重 Luminex®系统动态检测了 33 例 SFTS 患者发病后第 3-7 天、第 8-12 天和第 13-20 天的 36 种炎症介质的循环水平。在这些患者中,15 例重症患者痊愈,11 例重症患者在 3 周内死亡。我们发现 IL-1RA、IL-6、IL-15、IL-10、TNF-α、IFN-γ、G-CSF、嗜酸性粒细胞趋化因子、IL-8、IP-10、MCP-1、MIP-1α、MIP-1β 和 fractalkine 在 SFTS 患者中明显上调。SFTS 患者中升高的 IL-15 和嗜酸性粒细胞趋化因子是首次报道的。在第 1 周,死亡患者中同时存在最高水平的促炎和抗炎细胞因子。在死亡患者中,炎症介质一直处于高水平,而非死亡患者在 3 周内恢复正常。我们的结果表明,SFTS 患者炎症风暴的发生与 SFTS 的严重程度有关。RANTES 和 PDGF 下调,在整个疾病过程中在死亡患者中始终保持显著较低水平,RANTES 和 PDGF 的浓度与血小板计数呈显著正相关。我们的结果表明,失调的炎症反应与 SFTS 患者的疾病发病机制和死亡率有关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/edd0/5760584/8c49f16f026e/41598_2017_18616_Fig1_HTML.jpg

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