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一项观察性研究,探讨可溶性免疫检查点作为 COVID-19 重症的指标。

An observational study investigating soluble immune checkpoints as indicators of severe COVID-19.

机构信息

Facultad de Medicina Veterinaria y Zootecnia (FMVZ), Universidad Michoacana de San Nicolás de San Nicolás de Hidalgo (UMSNH), Morelia-Zinapécuaro, Mexico.

Centro de Investigación Biomédica de Michoacán, División de Investigación Clínica, Instituto Mexicano del Seguro Social, Morelia, Mexico.

出版信息

Microbiol Spectr. 2024 Jul 2;12(7):e0377623. doi: 10.1128/spectrum.03776-23. Epub 2024 May 29.

Abstract

This study aimed to investigate the immunomodulatory behavior of soluble immune checkpoints (sICPs) and other biomarkers in the pathophysiology of SARS-CoV-2 infection. The study included 59 adult participants, 43 of whom tested positive for SARS-CoV-2. Patients were divided into three cohorts: those with moderate disease ( = 16), recovered patients with severe disease ( = 13), and deceased patients with severe disease ( = 16). In addition, 16 participants were pre-pandemic subjects negative for SARS-CoV-2. The relative activity of neutralizing antibodies (rNAbs) against SARS-CoV-2 and the values of 14 sICPs in peripheral blood were compared between the four groups. Because the increase of markers values of inflammation [NLR > 12; CRP > 150 mg/L] and venous thromboembolism [D-dimer > 0.5 mg/L] has been associated with mortality from COVID-19, the total and differential leukocyte counts, the NLR, and CRP and D-dimer values were obtained in patients with severe disease. No differences in rNAbs were observed between the cohorts. Only the levels of five sICPs, sCD27, sHVEM sTIM-3, sPD-1, and sPDL-1, were significantly higher in patients with severe rather than moderate disease. The sPDL-2 level and NLR were higher in deceased patients than in recovered patients. However, there was no difference in CRP and D-dimer values between the two groups. Of the five soluble biomarkers compared among patients with severe disease, only sPDL-2 was higher in deceased patients than in recovered patients. This suggests that immuno-inhibitory sICPs might be used as indicators for severe COVID-19, with sPDL-2 used to assess individual risk for fatality.IMPORTANCECOVID-19, the disease caused by a SARS-CoV-2 infection, generates a broad spectrum of clinical symptoms, progressing to multiorgan failure in the most severe cases. As activation of the immune system is pivotal to eradicating the virus, future research should focus on identifying reliable biomarkers to efficiently predict the outcome in severe COVID-19 cases. Soluble immune checkpoints represent the function of the immune system and are easily determined in peripheral blood. This research could lead to implementing more effective severity biomarkers for COVID-19, which could increase patients' survival rate and quality of life.

摘要

本研究旨在探讨可溶性免疫检查点(sICPs)和其他生物标志物在 SARS-CoV-2 感染病理生理学中的免疫调节行为。该研究纳入了 59 名成年参与者,其中 43 名参与者的 SARS-CoV-2 检测呈阳性。患者被分为三组:中度疾病患者(n=16)、严重疾病康复患者(n=13)和严重疾病死亡患者(n=16)。此外,还有 16 名参与者为 SARS-CoV-2 阴性的大流行前受试者。比较了四组患者外周血中针对 SARS-CoV-2 的中和抗体(rNAbs)的相对活性和 14 种 sICPs 的水平。由于炎症标志物值[NLR>12;CRP>150mg/L]和静脉血栓栓塞标志物值[D-二聚体>0.5mg/L]的升高与 COVID-19 的死亡率相关,因此在严重疾病患者中获得了总白细胞计数、白细胞分类计数、NLR、CRP 和 D-二聚体值。在各组患者中,rNAbs 无差异。仅在严重疾病患者中,五种 sICPs(sCD27、sHVEM、sTIM-3、sPD-1 和 sPDL-1)的水平显著高于中度疾病患者。与康复患者相比,死亡患者的 sPDL-2 水平和 NLR 更高。然而,两组患者的 CRP 和 D-二聚体值无差异。在严重疾病患者中比较的五种可溶性生物标志物中,仅 sPDL-2 在死亡患者中高于康复患者。这表明免疫抑制性 sICPs 可作为严重 COVID-19 的指标,sPDL-2 可用于评估个体的致死风险。

重要性

由 SARS-CoV-2 感染引起的 COVID-19 疾病会产生广泛的临床症状,在最严重的情况下会导致多器官衰竭。由于免疫系统的激活对于消除病毒至关重要,因此未来的研究应集中于确定可靠的生物标志物,以有效地预测严重 COVID-19 病例的结果。可溶性免疫检查点代表免疫系统的功能,并且易于在外周血中确定。这项研究可以为 COVID-19 实施更有效的严重程度生物标志物,这可以提高患者的生存率和生活质量。

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