COVID-19肺炎重症监护病房患者体内有无中和I型干扰素的自身抗体,其肺部SARS-CoV-2负荷动力学相似。

IF 7.2 2区 医学 Q1 IMMUNOLOGY
Valentine Le Stang, Paul Bastard, Elise Langouet, Marc Pineton de Chambrun, Juliette Chommeloux, Adrian Gervais, Lucy Bizien, Anne Puel, Aurélie Cobat, Julien Mayaux, Alexandre Demoule, Jean-Laurent Casanova, David Boutolleau, Alain Combes, Sonia Burrel, Charles-Edouard Luyt
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引用次数: 0

摘要

目的:ICU患者中危及生命的2019年冠状病毒病(COVID-19)肺炎的发病机制可能涉及预先存在的中和I型干扰素(IFNs)的自身抗体(auto-Abs)。这些自身抗体对下呼吸道(LRT)中 SARS-CoV-2 清除率的影响尚不清楚:我们对 2020 年 3 月至 5 月间的 99 例 COVID-19 肺炎 ICU 患者进行了回顾性研究。根据是否存在中和 I 型 IFNs 的循环自身抗体分析了下呼吸道 SARS-CoV-2 负荷(强度和持续时间):结果:在纳入的 99 名患者中,38 人(38%)中和 I 型 IFN 的自身抗体呈阳性,其中 5 人(5%)携带中和任何浓度 IFN-α2 的自身抗体,33 人(33%)仅携带中和低浓度 IFN-ω 的自身抗体。有或没有中和 I 型 IFN 的自身抗体的患者,其 LRT 中的 SARS-CoV-2 载量和病毒脱落持续时间相似。有自身抗体的患者死亡率与无自身抗体的患者相同,尽管肾功能衰竭和 ECMO 支持的发生率更高,机械通气和重症监护病房的住院时间更长:总之,5% 的 COVID-19 重症肺炎患者携带中和 IFN-α2 的自身抗体,而约 1/3 的患者携带中和低浓度 IFN-ω 的自身抗体。两种自身抗体的检测结果均不影响 LRT 病毒清除率和死亡率,但与发病率增高和住院时间延长有关。这些研究结果表明,在没有IFN自身抗体的患者中,类似但迄今未知的疾病机制也会导致COVID-19重症肺炎。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Similar Kinetics of Pulmonary SARS-CoV-2 Load in Intensive Care Unit Patients with COVID-19 Pneumonia with or Without Autoantibodies Neutralizing Type I Interferons.

Purpose: 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.

Methods: 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.

Results: 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.

Conclusion: 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.

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来源期刊
CiteScore
12.20
自引率
9.90%
发文量
218
审稿时长
2 months
期刊介绍: The Journal of Clinical Immunology publishes impactful papers in the realm of human immunology, delving into the diagnosis, pathogenesis, prognosis, or treatment of human diseases. The journal places particular emphasis on primary immunodeficiencies and related diseases, encompassing inborn errors of immunity in a broad sense, their underlying genotypes, and diverse phenotypes. These phenotypes include infection, malignancy, allergy, auto-inflammation, and autoimmunity. We welcome a broad spectrum of studies in this domain, spanning genetic discovery, clinical description, immunologic assessment, diagnostic approaches, prognosis evaluation, and treatment interventions. Case reports are considered if they are genuinely original and accompanied by a concise review of the relevant medical literature, illustrating how the novel case study advances the field. The instructions to authors provide detailed guidance on the four categories of papers accepted by the journal.
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