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