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Differences in activation and tissue homing markers of natural killer cell subsets during acute dengue infection.在急性登革热感染期间自然杀伤细胞亚群的激活和组织归巢标志物的差异。
Immunology. 2018 Apr;153(4):455-465. doi: 10.1111/imm.12858. Epub 2017 Dec 11.
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Developmental and Functional Control of Natural Killer Cells by Cytokines.细胞因子对自然杀伤细胞的发育和功能控制
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Different features of Vδ2 T and NK cells in fatal and non-fatal human Ebola infections.在致命和非致命性人类埃博拉病毒感染中Vδ2 T细胞和自然杀伤细胞的不同特征
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Epidemiological Characteristics and Environmental Risk Factors of Severe Fever with Thrombocytopenia Syndrome in Hubei Province, China, from 2011 to 2016.2011年至2016年中国湖北省发热伴血小板减少综合征的流行病学特征及环境危险因素
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A simple and practical score model for predicting the mortality of severe fever with thrombocytopenia syndrome patients.一种用于预测严重发热伴血小板减少综合征患者死亡率的简单实用评分模型。
Medicine (Baltimore). 2016 Dec;95(52):e5708. doi: 10.1097/MD.0000000000005708.
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NK cells in host responses to viral infections.自然杀伤细胞在宿主对病毒感染的反应中。
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Decreased myeloid dendritic cells indicate a poor prognosis in patients with severe fever with thrombocytopenia syndrome.髓样树突状细胞减少表明严重发热伴血小板减少综合征患者预后不良。
Int J Infect Dis. 2017 Jan;54:113-120. doi: 10.1016/j.ijid.2016.11.418. Epub 2016 Nov 30.
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Decreased monocyte subsets and TLR4-mediated functions in patients with acute severe fever with thrombocytopenia syndrome (SFTS).急性严重发热伴血小板减少综合征(SFTS)患者单核细胞亚群减少和 TLR4 介导的功能障碍。
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Characterization of immunological responses in patients with severe fever with thrombocytopenia syndrome: a cohort study in China.严重发热伴血小板减少综合征患者免疫反应特征:一项中国的队列研究
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NK cell activation in human hantavirus infection explained by virus-induced IL-15/IL15Rα expression.病毒诱导的IL-15/IL15Rα表达解释了人类汉坦病毒感染中自然杀伤细胞的激活。
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严重发热伴血小板减少综合征病毒急性感染时 CD56CD16NK 细胞的耗竭和激活。

Depletion but Activation of CD56CD16 NK Cells in Acute Infection with Severe Fever with Thrombocytopenia Syndrome Virus.

机构信息

Department of Infectious Diseases, Institute of Infection and Immunology, Union Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, 430022, China.

Department of Gastroenterology, Henan Provincial People's Hospital, People's Hospital of Zhengzhou University, Zhengzhou, 450003, China.

出版信息

Virol Sin. 2020 Oct;35(5):588-598. doi: 10.1007/s12250-020-00224-3. Epub 2020 May 19.

DOI:10.1007/s12250-020-00224-3
PMID:32430872
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC7736421/
Abstract

Severe fever with thrombocytopenia syndrome (SFTS) is an emerging infectious disease with high mortality (12%-30%). The mechanism by which the SFTS bunyavirus (SFTSV) causes severe illness remains unclear. To evaluate the phenotypic and functional characteristics of the NK cell subsets in SFTS patients, twenty-nine SFTS patients were sequentially sampled from admission until recovery. Phenotypic and functional characteristics of NK cell subsets in circulating blood were analysed via flow cytometry. Then, correlations between NK cell subset frequencies and the SFTS index (SFTSI) were evaluated in all SFTS patients (15 mild, 14 severe) upon admission. The frequencies of CD56CD16 NK cells were greatly decreased in early SFTSV infection and were negatively correlated with disease severity. Additionally, higher Ki-67 and granzyme B expression and relatively lower NKG2A expression in CD56CD16 NK cells were observed in acute infection. Moreover, the effector function of CD56 NK cells was increased in the acute phase compared with the recovery phase in nine severe SFTS patients. Additionally, interleukin (IL)-15, interferon (IFN)-α, IL-18 and IFN-γ secretion was markedly increased during early infection. Collectively, despite depletion of CD56CD16 NK cells, activation and functional enhancement of CD56CD16 NK cells were still observed, suggesting their involvement in defence against early SFTSV infection.

摘要

严重发热伴血小板减少综合征(SFTS)是一种具有高死亡率(12%-30%)的新发传染病。SFTS 病毒(SFTSV)引起严重疾病的机制尚不清楚。为了评估 SFTS 患者 NK 细胞亚群的表型和功能特征,我们连续从入院到康复对 29 例 SFTS 患者进行了采样。通过流式细胞术分析循环血液中 NK 细胞亚群的表型和功能特征。然后,在所有 SFTS 患者(15 例轻症,14 例重症)入院时评估 NK 细胞亚群频率与 SFTS 指数(SFTSI)之间的相关性。在早期 SFTSV 感染中,CD56CD16 NK 细胞的频率大大降低,与疾病严重程度呈负相关。此外,在急性感染中观察到 CD56CD16 NK 细胞中的 Ki-67 和颗粒酶 B 表达较高,而 NKG2A 表达较低。此外,在 9 例重症 SFTS 患者中,CD56 NK 细胞的效应功能在急性期较恢复期增加。此外,在早期感染期间,白细胞介素(IL)-15、干扰素(IFN)-α、IL-18 和 IFN-γ的分泌明显增加。总之,尽管 CD56CD16 NK 细胞耗竭,但仍观察到 CD56CD16 NK 细胞的激活和功能增强,表明其参与了对早期 SFTSV 感染的防御。