Department of Infectious Diseases, Qilu Hospital of Shandong University, Wenhua Xi Road 107, Jinan, Shandong, 250012, China.
Department of Infectious Diseases, Shandong Public Health Clinical Center, Lieshishan Dong Road 11, Jinan, Shandong, 250102, China.
Virol J. 2024 Jun 3;21(1):126. doi: 10.1186/s12985-024-02403-0.
Severe fever with thrombocytopenia syndrome (SFTS) is an emerging infectious disease caused by severe fever with thrombocytopenia syndrome virus (SFTSV). Previous studies have indicated that SFTS patients have a high mortality rate, which may be related to cytokine storm and immune dysfunction. In our study, we analyzed differences in cytokines and lymphocyte subsets between severe and non-severe SFTS patients, with the aim of identifying predictors of severity.
We retrospectively analyzed demographic characteristics, clinical data, cytokine profiles, and lymphocyte subsets from 96 laboratory confirmed SFTS patients between April 2021 and August 2023.
A total of 96 SFTS patients were enrolled, with a mean age of 65.05 (± 7.92) years old. According to our grouping criteria, 35 (36.5%) of these patients were classified as severe group, while 61 (63.5%) were classified as non-severe group. Univariate analysis revealed that age, interleukin-6 (IL-6), interleukin-8 (IL-8), interleukin-10 (IL-10), interferon-α (IFN-α), CD4 + T cell, and CD8 + T cell counts were risk predictors for the severity of SFTS. Further multivariable logistic regression analysis confirmed age, IL-6 levels, and CD4 + T cell counts as independent predictors of SFTS severity.
Severe SFTS patients may experience cytokine storms and immune dysfunction. Aging, elevated levels of IL-6, and decreased CD4 + T cell count may serve as independent predictors for the severity of SFTS.
发热伴血小板减少综合征(SFTS)是一种新发传染病,由发热伴血小板减少综合征病毒(SFTSV)引起。先前的研究表明,SFTS 患者的死亡率较高,这可能与细胞因子风暴和免疫功能障碍有关。在本研究中,我们分析了重症和非重症 SFTS 患者之间细胞因子和淋巴细胞亚群的差异,旨在确定疾病严重程度的预测因子。
我们回顾性分析了 2021 年 4 月至 2023 年 8 月期间 96 例实验室确诊的 SFTS 患者的人口统计学特征、临床数据、细胞因子谱和淋巴细胞亚群。
共纳入 96 例 SFTS 患者,平均年龄为 65.05(±7.92)岁。根据我们的分组标准,其中 35 例(36.5%)患者为重症组,61 例(63.5%)为非重症组。单因素分析显示,年龄、白细胞介素-6(IL-6)、白细胞介素-8(IL-8)、白细胞介素-10(IL-10)、干扰素-α(IFN-α)、CD4+T 细胞和 CD8+T 细胞计数是 SFTS 严重程度的危险因素。进一步的多变量逻辑回归分析证实,年龄、IL-6 水平和 CD4+T 细胞计数是 SFTS 严重程度的独立预测因子。
重症 SFTS 患者可能发生细胞因子风暴和免疫功能障碍。年龄增长、IL-6 水平升高和 CD4+T 细胞计数减少可能是 SFTS 严重程度的独立预测因子。