Department of Critical Care Medicine, State Key Laboratory of Complex Severe and Rare Diseases, Peking Union Medical College Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Beijing, China.
Department of Critical Care Medicine, Beijing Jishuitan Hospital, Beijing, China.
Front Immunol. 2022 Jul 11;13:938538. doi: 10.3389/fimmu.2022.938538. eCollection 2022.
There is evidence that metabolic disorder, dysfunction and abnormal apoptosis of immune cells are closely related to immunosuppression in sepsis. Single monitoring of exhaustion receptors does not reflect well the immune status of septic patients; therefore, we monitored immune status in relation to metabolism, function and apoptosis of immune cells to find good prognostic indicators for sepsis.
A single-center prospective observational study.
Teaching hospital including an academic tertiary care center.
81 patients with sepsis and 22 without sepsis admitted to the ICU.
Patients were divided according to Sequential Organ Failure Assessment (SOFA) score: mild sepsis 2-5 points and severe sepsis ≥6 points. SOFA score was recalculated daily. If it changed by ≥2 points within 2 days, T-cell metabolism, function and apoptotic makers [mammalian target of rapamycin (mTOR), T-bet, interferon (IFN)-γ, granzyme B, and programmed cell death (PD)-1] were continuously monitored on days 1, 3 and 5 after admission.
The overall status of immune cells was compared among patients with different severity of sepsis. Patients with severe sepsis, compared with mild and no sepsis, had lower lymphocyte counts, higher expression of receptors associated with cell metabolism, activation and apoptosis, and lower expression of functional receptors. Multivariate regression analysis revealed that frequency of CD4 T cells expressing mTOR, IFN-γ and PD-1 at admission was an independent predictor of 28-day mortality. Receiver operating characteristic curve analysis indicated that frequency of CD4 T cells expressing mTOR, IFN-γ and PD-1 predicted 28-day mortality, with cutoffs of 30.57%, 12.81% and 22.46%, respectively. The expression of related receptors on CD8+ T cells showed similar trend to that on CD4+ T cells, but no significant difference was found.
Abnormally increased expression of metabolic and apoptotic receptors on CD4 T cells and decreased expression of functional factors are associated with poor prognosis in ICU patients with sepsis. Poor prognosis can be identified by early detection of expression of mammalian target of rapamycin (mTOR), IFN-γ and PD-1 on CD4 T cells.
有证据表明,代谢紊乱、免疫细胞功能障碍和异常凋亡与脓毒症中的免疫抑制密切相关。单独监测耗竭受体不能很好地反映脓毒症患者的免疫状态;因此,我们监测了与免疫细胞代谢、功能和凋亡相关的免疫状态,以寻找脓毒症的良好预后指标。
一项单中心前瞻性观察研究。
包括学术型三级护理中心的教学医院。
81 例脓毒症患者和 22 例非脓毒症患者入住 ICU。
根据序贯器官衰竭评估(SOFA)评分将患者分为:轻度脓毒症 2-5 分和重度脓毒症≥6 分。每天重新计算 SOFA 评分。如果在 2 天内变化≥2 分,则在入院后第 1、3 和 5 天连续监测 T 细胞代谢、功能和凋亡标志物[雷帕霉素靶蛋白(mTOR)、T 细胞转录因子(T-bet)、干扰素(IFN)-γ、颗粒酶 B 和程序性细胞死亡(PD)-1]。
比较了不同严重程度脓毒症患者之间免疫细胞的整体状态。与轻度和无脓毒症患者相比,重度脓毒症患者的淋巴细胞计数较低,与细胞代谢、激活和凋亡相关的受体表达较高,而功能受体表达较低。多变量回归分析显示,入院时 CD4 T 细胞表达 mTOR、IFN-γ 和 PD-1 的频率是 28 天死亡率的独立预测因子。受试者工作特征曲线分析表明,CD4 T 细胞表达 mTOR、IFN-γ 和 PD-1 的频率预测 28 天死亡率,截断值分别为 30.57%、12.81%和 22.46%。CD8+T 细胞上相关受体的表达趋势与 CD4+T 细胞相似,但无显著差异。
CD4 T 细胞代谢和凋亡受体异常高表达,功能因子表达降低,与 ICU 脓毒症患者预后不良相关。通过早期检测 CD4 T 细胞上 mTOR、IFN-γ 和 PD-1 的表达,可以识别预后不良。