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登革病毒感染导致 IgM 阳性个体中血栓素 A2 水平升高与登革热的轻度症状有关。

Increased Levels of Txa₂ Induced by Dengue Virus Infection in IgM Positive Individuals Is Related to the Mild Symptoms of Dengue.

机构信息

Imunologia Celular e Molecular, Instituto René Rachou, Avenida Augusto de Lima, 1715, sala 406, Belo Horizonte 30190-002, Brazil.

Santa Casa de Misericórdia de Santo Antônio do Monte, Santo Antônio do Monte 35560-000, Brazil.

出版信息

Viruses. 2018 Feb 28;10(3):104. doi: 10.3390/v10030104.

DOI:10.3390/v10030104
PMID:29495587
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5869497/
Abstract

The inflammatory process plays a major role in the prognosis of dengue. In this context, the eicosanoids may have considerable influence on the regulation of the -induced inflammatory process. To quantify the molecules involved in the cyclooxygenase and lipoxygenase pathways during infection, plasma levels of thromboxane A2, prostaglandin E2 and leukotriene B4; mRNA levels of thromboxane A2 synthase, prostaglandin E2 synthase, leukotriene A4 hydrolase, cyclooxygenase-2 and 5-lipoxygenase; and the levels of lipid bodies in peripheral blood leukocytes collected from IgM-positive and IgM-negative volunteers with mild dengue, and non-infected volunteers, were evaluated. infection increases the levels of thromboxane A2 in IgM-positive individuals as well as the amount of lipid bodies in monocytes in IgM-negative individuals. We suggest that increased levels of thromboxane A2 in IgM-positive individuals plays a protective role against the development of severe symptoms of dengue, such as vascular leakage.

摘要

炎症过程在登革热的预后中起着重要作用。在这种情况下,类二十烷酸可能对调节登革热诱导的炎症过程有相当大的影响。为了定量检测 感染过程中环氧化酶和脂氧化酶途径中涉及的分子,我们检测了来自 IgM 阳性和 IgM 阴性的轻度登革热患者以及未感染志愿者的血浆血栓素 A2、前列腺素 E2 和白三烯 B4 水平;血栓素 A2 合酶、前列腺素 E2 合酶、白三烯 A4 水解酶、环氧合酶-2 和 5-脂氧合酶的 mRNA 水平;以及外周血白细胞中的脂滴水平。 感染增加了 IgM 阳性个体的血栓素 A2 水平,以及 IgM 阴性个体单核细胞中的脂滴数量。我们认为,IgM 阳性个体中血栓素 A2 水平的升高对防止登革热的严重症状(如血管渗漏)的发展起到了保护作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7b0/5869497/3349e932d810/viruses-10-00104-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7b0/5869497/bf8bc0e698d6/viruses-10-00104-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7b0/5869497/c40b16a73ab9/viruses-10-00104-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7b0/5869497/cfcc4bcdf42b/viruses-10-00104-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7b0/5869497/c2b4378c29ed/viruses-10-00104-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7b0/5869497/3349e932d810/viruses-10-00104-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7b0/5869497/bf8bc0e698d6/viruses-10-00104-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7b0/5869497/c40b16a73ab9/viruses-10-00104-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7b0/5869497/cfcc4bcdf42b/viruses-10-00104-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7b0/5869497/c2b4378c29ed/viruses-10-00104-g004a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7b0/5869497/3349e932d810/viruses-10-00104-g005.jpg

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本文引用的文献

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J Neuroinflammation. 2017 Aug 14;14(1):158. doi: 10.1186/s12974-017-0931-5.
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The impact of Wolbachia infection on the rate of vertical transmission of dengue virus in Brazilian Aedes aegypti.沃尔巴克氏体感染对巴西埃及伊蚊中登革病毒垂直传播率的影响。
Parasit Vectors. 2017 Jun 17;10(1):296. doi: 10.1186/s13071-017-2236-z.
3
Pathogenesis of vascular leak in dengue virus infection.登革病毒感染中血管渗漏的发病机制。
Immunology. 2017 Jul;151(3):261-269. doi: 10.1111/imm.12748. Epub 2017 May 24.
4
Cyclooxygenase-2 facilitates dengue virus replication and serves as a potential target for developing antiviral agents.环氧化酶-2 促进登革热病毒复制,可作为开发抗病毒药物的潜在靶点。
Sci Rep. 2017 Mar 20;7:44701. doi: 10.1038/srep44701.
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Platelet activation determines the severity of thrombocytopenia in dengue infection.血小板活化决定登革热感染中血小板减少症的严重程度。
Sci Rep. 2017 Jan 31;7:41697. doi: 10.1038/srep41697.
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Current management of severe dengue infection.重症登革热感染的当前管理。
Expert Rev Anti Infect Ther. 2017 Jan;15(1):67-78. doi: 10.1080/14787210.2017.1248405. Epub 2016 Oct 27.
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Dengue infection.登革热感染。
Nat Rev Dis Primers. 2016 Aug 18;2:16055. doi: 10.1038/nrdp.2016.55.
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Recent advances in dengue pathogenesis and clinical management.登革热发病机制与临床管理的最新进展
Vaccine. 2015 Dec 10;33(50):7061-8. doi: 10.1016/j.vaccine.2015.09.103. Epub 2015 Oct 14.
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