Médecine Intensive Réanimation, Sorbonne Université, Groupe Hospitalier Pitié-Salpêtrière, Assistance Publique - Hôpitaux de Paris (AP-HP), Paris, France.
St. Giles Laboratory of Human Genetics of Infectious Diseases, Rockefeller Branch, The Rockefeller University, New York, NY, USA.
J Clin Immunol. 2024 Nov 20;45(1):45. doi: 10.1007/s10875-024-01839-x.
The pathogenesis of life-threatening coronavirus disease 2019 (COVID-19) pneumonia in ICU patients can involve pre-existing auto-antibodies (auto-Abs) neutralizing type I interferons (IFNs). The impact of these auto-Abs on SARS-CoV-2 clearance in the lower respiratory tract (LRT) is unclear.
We performed a retrospective study in 99 ICU patients with COVID-19 pneumonia between March and May 2020. LRT SARS-CoV-2 load (intensity and duration) was analyzed according to the presence or not of circulating auto-Abs neutralizing type I IFNs.
Among the 99 included patients, 38 (38%) were positive for auto-Abs neutralizing type I IFNs, with 5 (5%) harboring auto-Abs neutralizing IFN-α2 at any concentration, while 33 (33%) had auto-Abs neutralizing only IFN-ω at the lower concentration. SARS-CoV-2 load in the LRT and duration of viral shedding, were similar in patients with or without auto-Abs neutralizing type I IFNs. Patients with auto-Abs had the same mortality than those without auto-Abs, despite greater occurrence of renal failure and ECMO support, and longer duration of mechanical ventilation and ICU stay.
In summary, 5% of patients with critical COVID-19 pneumonia carried auto-Abs neutralizing IFN-α2, while about 1/3 harbored auto-Abs neutralizing low concentrations of IFN-ω. The detection of either type of auto-Abs did not impact LRT viral clearance and mortality, although it was associated with greater morbidity and a longer hospitalization. These findings suggest that similar albeit hitherto unknown mechanisms of disease drive critical COVID-19 pneumonia in patients without auto-Abs against type I IFNs.
危重症 2019 年冠状病毒病(COVID-19)肺炎患者的发病机制可能涉及中和 I 型干扰素(IFN)的预先存在的自身抗体(auto-Abs)。这些自身抗体对下呼吸道(LRT)中 SARS-CoV-2 的清除的影响尚不清楚。
我们对 2020 年 3 月至 5 月期间 99 例 COVID-19 肺炎 ICU 患者进行了回顾性研究。根据是否存在循环中和 I 型 IFN 的自身抗体,分析 LRT SARS-CoV-2 负荷(强度和持续时间)。
在 99 例纳入的患者中,38 例(38%)自身抗体中和 I 型 IFN 阳性,其中 5 例(5%)任何浓度均存在中和 IFN-α2 的自身抗体,而 33 例(33%)仅在低浓度下存在中和 IFN-ω 的自身抗体。LRT 中的 SARS-CoV-2 负荷和病毒脱落持续时间在存在或不存在中和 I 型 IFN 的自身抗体的患者中相似。尽管肾衰竭和 ECMO 支持的发生率更高,机械通气和 ICU 住院时间更长,但具有自身抗体的患者与没有自身抗体的患者死亡率相同。
总之,5%的危重症 COVID-19 肺炎患者携带中和 IFN-α2 的自身抗体,而约 1/3 患者携带中和低浓度 IFN-ω 的自身抗体。无论哪种类型的自身抗体的检测都不会影响 LRT 病毒清除和死亡率,但与更高的发病率和更长的住院时间有关。这些发现表明,在没有针对 I 型 IFN 的自身抗体的患者中,导致严重 COVID-19 肺炎的疾病机制相似,尽管尚不清楚。