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降低中东呼吸综合征冠状病毒感染患者血浆中可溶性二肽基肽酶 4 水平。

Reduction of soluble dipeptidyl peptidase 4 levels in plasma of patients infected with Middle East respiratory syndrome coronavirus.

机构信息

Department of Pharmaceutical Science, College of Pharmacy, Kyung Hee University, Seoul, Republic of Korea.

Department of Microbiology and Immunology, College of Medicine, Seoul National University, 103 Daehak-ro, Jongno-gu, Seoul 03080, Republic of Korea; Department of Biomedical Sciences, College of Medicine, Seoul National University, Seoul, Republic of Korea.

出版信息

Virology. 2018 May;518:324-327. doi: 10.1016/j.virol.2018.03.015. Epub 2018 Mar 26.

Abstract

Dipeptidyl peptidase 4 (DPP4) is a receptor for MERS-CoV. The soluble form of DPP4 (sDPP4) circulates systematically and can competitively inhibit MERS-CoV entry into host cells. Here, we measured the concentration of sDPP4 in the plasma and sputa of 14 MERS-CoV-infected patients of various degrees of disease severity. The concentration of sDPP4 in the plasma of MERS patients (474.76 ± 108.06 ng/ml) was significantly lower than those of healthy controls (703.42 ± 169.96 ng/ml), but there were no significant differences among the patient groups. Interestingly, plasma levels of IL-10 and EGF were negatively and positively correlated with sDPP4 concentrations, respectively. The sDPP4 levels in sputa were less than 300 ng/ml. Viral infection was inhibited by 50% in the presence of more than 8000 ng/ml of sDPP4. Therefore, sDPP4 levels in the plasma of MERS patients are significantly reduced below the threshold needed to exert an antiviral effect against MERS-CoV infection.

摘要

二肽基肽酶 4(DPP4)是中东呼吸综合征冠状病毒(MERS-CoV)的受体。DPP4 的可溶性形式(sDPP4)在系统中循环,并能竞争性抑制 MERS-CoV 进入宿主细胞。在此,我们测量了 14 位不同严重程度的 MERS-CoV 感染患者的血浆和痰液中 sDPP4 的浓度。MERS 患者血浆中 sDPP4 的浓度(474.76±108.06ng/ml)明显低于健康对照者(703.42±169.96ng/ml),但患者组之间无显著差异。有趣的是,血浆中白细胞介素 10(IL-10)和表皮生长因子(EGF)的水平与 sDPP4 浓度呈负相关和正相关。痰液中的 sDPP4 水平低于 300ng/ml。当 sDPP4 浓度超过 8000ng/ml 时,病毒感染被抑制了 50%。因此,MERS 患者血浆中的 sDPP4 水平明显降低到对 MERS-CoV 感染发挥抗病毒作用所需的阈值以下。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/287e/7112025/8735eb616230/gr1_lrg.jpg

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