Department of Clinical Infectious Diseases, Toyama University Graduate School of Medicine and Pharmaceutical Sciences, Toyama, Japan.
Department of Microbiology, Toyama University Graduate School of Medicine and Pharmaceutical Sciences, Toyama, Japan.
Front Immunol. 2022 Feb 14;13:844304. doi: 10.3389/fimmu.2022.844304. eCollection 2022.
The role of type I interferons (IFNs) in the early phase of COVID-19 remains unclear.
To evaluate the relationship between IFN-I levels in patients with COVID-19 and clinical presentation, SARS-CoV-2 viral load, and other major pro-inflammatory cytokines.
This prospective observational study recruited patients hospitalized with COVID-19. The levels of interferon-alpha (IFN-α), interferon-beta (IFN-β), interleukin-6 (IL-6), and C-X-C motif chemokine ligand (CXCL10) within 5 days after symptom onset were measured using an ELISA, in serum from blood collected within 5 days after the onset of symptoms. The SARS-CoV-2 viral load was determined qPCR using nasal-swab specimens and serum.
The study enrolled 50 patients with COVID-19. IFN-α levels were significantly higher in patients who presented with pneumonia or developed hypoxemic respiratory failure (p < 0.001). Furthermore, IFN-α levels were associated with viral load in nasal-swab specimens and RNAemia (p < 0.05). In contrast, there was no significant association between IFN-β levels and the presence of pneumonia or RNAemia, despite showing a stronger association with nasal-swab viral load (p < 0.001). Correlation analysis showed that the serum levels of IFN-α significantly correlated with those of IFN-β, IL-6, and CXCL10, while the levels of IFN-β did not correlate with those of IL-6 or CXCL10.
Serum IFN-I levels in the early phase of SARS-CoV-2 infection were higher in patients who developed hypoxemic respiratory failure. The association between IFN-α, IL-6, and CXCL10 may reflect the systemic immune response against SARS-CoV-2 invasion into pulmonary circulation, which might be an early predictor of respiratory failure due to COVID-19.
I 型干扰素(IFN-I)在 COVID-19 早期阶段的作用尚不清楚。
评估 COVID-19 患者 IFN-I 水平与临床表型、SARS-CoV-2 病毒载量和其他主要促炎细胞因子之间的关系。
这项前瞻性观察性研究招募了因 COVID-19 住院的患者。在症状出现后 5 天内,通过 ELISA 检测血清中干扰素-α(IFN-α)、干扰素-β(IFN-β)、白细胞介素-6(IL-6)和 C-X-C 基序趋化因子配体(CXCL10)的水平,采集血液样本在症状出现后 5 天内。使用鼻拭子标本和血清通过 qPCR 测定 SARS-CoV-2 病毒载量。
这项研究纳入了 50 名 COVID-19 患者。出现肺炎或发生低氧性呼吸衰竭的患者 IFN-α 水平显著升高(p<0.001)。此外,IFN-α 水平与鼻拭子标本中的病毒载量和 RNAemia 相关(p<0.05)。相比之下,IFN-β 水平与肺炎或 RNAemia 的发生无显著相关性,尽管与鼻拭子病毒载量的相关性更强(p<0.001)。相关性分析显示,IFN-α 的血清水平与 IFN-β、IL-6 和 CXCL10 的血清水平显著相关,而 IFN-β 的水平与 IL-6 或 CXCL10 的水平无相关性。
SARS-CoV-2 感染早期患者的血清 IFN-I 水平在发生低氧性呼吸衰竭的患者中更高。IFN-α、IL-6 和 CXCL10 之间的关联可能反映了针对 SARS-CoV-2 入侵肺循环的全身性免疫反应,这可能是 COVID-19 导致呼吸衰竭的早期预测指标。