Department of Emergency, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Department of Critical Care Medicine, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangzhou, China.
Shock. 2022 Aug 1;58(2):111-118. doi: 10.1097/SHK.0000000000001967. Epub 2022 Jul 30.
The expression of programmed cell death 1 receptor (PD-1) and CD28 on CD8+ T cells is considered to be related to immune function and prognosis markers in patients with sepsis. However, the relationship between the ratio of PD-1/CD28 and nosocomial infection has not been elucidated. Methods: A prospective, observational cohort study was conducted in a general intensive care unit. Patients were enrolled according to the sepsis-3 criteria and peripheral blood samples were collected within 24 hours of enrollment. Programmed cell death 1 receptor and CD28 expression on CD8+ T cells was assayed on day 1. Patients were followed up until 28 days. Multivariate regression analysis was used to assess independent risk factors for nosocomial infection. The accuracy of biomarkers for nosocomial infection and mortality was determined by the area under the receiver operating characteristic curve analysis. The association between biomarkers and 28-day mortality was assessed by Cox regression survival analysis. Results: A total of 181 patients were recruited, and 68 patients were finally included for analysis. Of these, 19 patients (27.9%) died during 28 days and 22 patients (32.4%) acquired nosocomial infection. The PD-1/CD28 ratio of patients with nosocomial infection was significantly higher than those without (0.27 [0.10-0.55] vs. 0.15 [0.08-0.28], P = 0.025). The PD-1/CD28 ratio in CD8+ T cells (odds ratio, 53.33; 95% confidence interval, 2.39-1188.22, P = 0.012) and duration of mechanical ventilation (odds ratio, 1.14; 95% confidence interval, 1.06-1.24; P = 0.001) were independently associated with nosocomial infection. The area under the receiver operating characteristic curve of PD-1/CD28 ratio in CD8+ T cells was 0.67 (0.52-0.82). The PD-1/CD28 ratio in CD8+ T cells of the nonsurvivors was significantly higher than the survivors (0.23 [0.15-0.52] vs. 0.14 [0.07-0.32]); Cox regression analysis showed that the survival time of patients with PD-1/CD28 ratio in CD8+ T cells of 0.13 or greater was shorter compared with patients with lower levels (hazard ratio, 4.42 [1.29-15.20], χ2 = 6.675; P = 0.010). Conclusions: PD-1/CD28 ratio in CD8+ T cells at admission may serve as a novel prognostic biomarker for predicting nosocomial infection and mortality.
程序性细胞死亡受体 1(PD-1)和 CD28 在 CD8+T 细胞上的表达被认为与脓毒症患者的免疫功能和预后标志物有关。然而,PD-1/CD28 比值与医院感染之间的关系尚未阐明。
采用前瞻性观察性队列研究,在普通重症监护病房进行。根据脓毒症 3 标准入选患者,并在入选后 24 小时内采集外周血样本。第 1 天检测 CD8+T 细胞上的 PD-1 和 CD28 的表达。对患者进行随访,直到 28 天。采用多变量回归分析评估医院感染的独立危险因素。采用受试者工作特征曲线分析评估生物标志物对医院感染和死亡率的准确性。采用 Cox 回归生存分析评估生物标志物与 28 天死亡率的关系。
共纳入 181 例患者,最终纳入 68 例患者进行分析。其中,27.9%(19/68)的患者在 28 天内死亡,32.4%(22/68)的患者发生医院感染。发生医院感染的患者 PD-1/CD28 比值明显高于未发生医院感染的患者(0.27[0.10-0.55]比 0.15[0.08-0.28],P=0.025)。CD8+T 细胞中 PD-1/CD28 比值(比值比,53.33;95%置信区间,2.39-1188.22,P=0.012)和机械通气时间(比值比,1.14;95%置信区间,1.06-1.24;P=0.001)与医院感染独立相关。CD8+T 细胞中 PD-1/CD28 比值的受试者工作特征曲线下面积为 0.67(0.52-0.82)。非幸存者的 CD8+T 细胞中 PD-1/CD28 比值明显高于幸存者(0.23[0.15-0.52]比 0.14[0.07-0.32]);Cox 回归分析显示,CD8+T 细胞中 PD-1/CD28 比值为 0.13 或更高的患者的生存时间短于比值较低的患者(风险比,4.42[1.29-15.20],χ2=6.675;P=0.010)。
入院时 CD8+T 细胞中 PD-1/CD28 比值可作为预测医院感染和死亡率的新型预后生物标志物。