Immunopathology Unit, National Center of Microbiology, Instituto de Salud Carlos III, 28029 Madrid, Spain.
Faculty of Sciences, Universidad de Alcalá, 28805 Madrid, Spain.
Int J Environ Res Public Health. 2023 Jan 20;20(3):1947. doi: 10.3390/ijerph20031947.
The main objective of this study was to determine the influence of the cytotoxic activity of peripheral blood mononuclear cells (PBMCs) on the outcome of unvaccinated individuals with critical COVID-19 admitted to the ICU. Blood samples from 23 individuals were collected upon admission and then every 2 weeks for 13 weeks until death (Exitus group) ( = 13) or discharge (Survival group) ( = 10). We did not find significant differences between groups in sociodemographic, clinical, or biochemical data that may influence the fatal outcome. However, direct cellular cytotoxicity of PBMCs from individuals of the Exitus group against pseudotyped SARS-CoV-2-infected Vero E6 cells was significantly reduced upon admission (-2.69-fold; = 0.0234) and after 4 weeks at the ICU (-5.58-fold; = 0.0290), in comparison with individuals who survived, and it did not improve during hospitalization. In vitro treatment with IL-15 of these cells did not restore an effective cytotoxicity at any time point until the fatal outcome, and an increased expression of immune exhaustion markers was observed in NKT, CD4+, and CD8+ T cells. However, IL-15 treatment of PBMCs from individuals of the Survival group significantly increased cytotoxicity at Week 4 (6.18-fold; = 0.0303). Consequently, immunomodulatory treatments that may overcome immune exhaustion and induce sustained, efficient cytotoxic activity could be essential for survival during hospitalization due to critical COVID-19.
本研究的主要目的是确定外周血单核细胞(PBMCs)的细胞毒性活性对未接种疫苗的危重新冠肺炎患者入住 ICU 的结局的影响。在入住时以及之后的 13 周内,每两周采集 23 名个体的血液样本,直到死亡(死亡组)(n = 13)或出院(存活组)(n = 10)。我们未发现可能影响致命结局的社会人口学、临床或生化数据在两组之间存在显著差异。然而,死亡组个体的 PBMCs 对假型 SARS-CoV-2 感染的 Vero E6 细胞的直接细胞毒性活性在入住时(-2.69 倍;p = 0.0234)和入住 ICU 4 周后(-5.58 倍;p = 0.0290)显著降低,与存活者相比,并且在住院期间并未改善。在体外用白细胞介素 15 处理这些细胞,直至致命结局,均未恢复有效的细胞毒性,并且在 NKT、CD4+和 CD8+T 细胞中观察到免疫衰竭标志物的表达增加。然而,在第 4 周,白细胞介素 15 处理存活组个体的 PBMCs 显著增加了细胞毒性(6.18 倍;p = 0.0303)。因此,由于严重的 COVID-19,免疫调节治疗可能克服免疫衰竭并诱导持续有效的细胞毒性活性,对于住院期间的生存至关重要。