Department of Pulmonary Medicine, Miguel Servet University Hospital, CIBERES, Instituto de Investigación Sanitaria (ISS) Aragón, Avenida Isabel la Católica 1-9, 50009, Zaragoza, Spain.
Department of Biochemistry, San Jorge Hospital, Huesca, Spain.
Respir Res. 2024 Jan 19;25(1):48. doi: 10.1186/s12931-023-02650-9.
Neutrophil extracellular traps (NETs) have repeatedly been related to COVID-19 severity and mortality. However, there is no consensus on their quantification, and there are scarce data on their evolution during the disease. We studied circulating NET markers in patients with COVID-19 throughout their hospitalization.
We prospectively included 93 patients (201 blood samples), evaluating the disease severity in 3 evolutionary phases (viral, early, and late inflammation). Of these, 72 had 180 samples in various phases. We also evaluated 55 controls with similar age, sex and comorbidities. We measured 4 NET markers in serum: cfDNA, CitH3, and MPO-DNA and NE-DNA complexes; as well as neutrophil-related cytokines IL-8 and G-CSF.
The COVID-19 group had higher CitH3 (28.29 vs 20.29 pg/mL, p = 0.022), and cfDNA, MPO-DNA, and NE-DNA (7.87 vs 2.56 ng/mL; 0.80 vs 0.52 and 1.04 vs 0.72, respectively, p < 0.001 for all) than the controls throughout hospitalisation. cfDNA was the only NET marker clearly related to severity, and it remained higher in non-survivors during the 3 phases. Only cfDNA was an independent risk factor for mortality and need for intensive care. Neutrophil count, IL-8, and G-CSF were significantly related to severity. MPO-DNA and NE-DNA showed significant correlations (r: 0.483, p < 0.001), including all 3 phases and across all severity grades, and they only remained significantly higher on days 10-16 of evolution in those who died. Correlations among the other NET markers were lower than expected.
The circulating biomarkers of NETs were present in patients with COVID-19 throughout hospitalization. cfDNA was associated with severity and mortality, but the three other markers showed little or no association with these outcomes. Neutrophil activity and neutrophil count were also associated with severity. MPO-DNA and NE-DNA better reflected NET formation. cfDNA appeared to be more associated with overall tissue damage; previous widespread use of this marker could have overestimated the relationship between NETs and severity. Currently, there are limitations to accurate NET markers measurement that make it difficult to assess its true role in COVID-19 pathogenesis.
中性粒细胞胞外诱捕网(NETs)与 COVID-19 的严重程度和死亡率密切相关。然而,目前还没有关于其定量检测的共识,也缺乏关于其在疾病过程中演变的数据。我们研究了 COVID-19 患者在整个住院期间的循环 NET 标志物。
我们前瞻性纳入了 93 例患者(201 份血样),在 3 个进化阶段(病毒、早期和晚期炎症)评估疾病严重程度。其中,72 例患者在不同阶段有 180 个样本。我们还评估了 55 名年龄、性别和合并症相似的对照组。我们测量了血清中的 4 种 NET 标志物:cfDNA、CitH3、MPO-DNA 和 NE-DNA 复合物;以及中性粒细胞相关细胞因子 IL-8 和 G-CSF。
COVID-19 组的 CitH3(28.29 vs 20.29 pg/mL,p=0.022)和 cfDNA、MPO-DNA、NE-DNA(7.87 vs 2.56 ng/mL;0.80 vs 0.52 和 1.04 vs 0.72,均 p<0.001)均高于对照组,在整个住院期间。cfDNA 是唯一与严重程度明显相关的 NET 标志物,在 3 个阶段非幸存者中仍保持较高水平。只有 cfDNA 是死亡率和需要重症监护的独立危险因素。中性粒细胞计数、IL-8 和 G-CSF 与严重程度显著相关。MPO-DNA 和 NE-DNA 之间存在显著相关性(r:0.483,p<0.001),包括所有 3 个阶段和所有严重程度等级,并且仅在死亡患者的第 10-16 天仍显著升高。其他 NET 标志物之间的相关性低于预期。
COVID-19 患者在整个住院期间都存在循环 NET 标志物。cfDNA 与严重程度和死亡率相关,但其他 3 个标志物与这些结果的相关性较小或没有相关性。中性粒细胞活性和中性粒细胞计数也与严重程度相关。MPO-DNA 和 NE-DNA 更能反映 NET 的形成。cfDNA 似乎与整体组织损伤的关系更密切;之前对这种标志物的广泛应用可能高估了 NETs 与严重程度之间的关系。目前,准确测量 NET 标志物存在局限性,难以评估其在 COVID-19 发病机制中的真正作用。