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肺保护与感染清除:白细胞介素 10 被怀疑在 COVID-19 中两面三刀。

Lung Protection vs. Infection Resolution: Interleukin 10 Suspected of Double-Dealing in COVID-19.

机构信息

Department of Anesthesiology and Surgical Intensive Care Medicine, Medical Faculty Mannheim, University Medical Center Mannheim, Mannheim Institute for Innate Immunoscience (MI3), Heidelberg University, Mannheim, Germany.

出版信息

Front Immunol. 2021 Mar 3;12:602130. doi: 10.3389/fimmu.2021.602130. eCollection 2021.

Abstract

The pathological processes by severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection that make the virus a major threat to global health are insufficiently understood. Inefficient viral clearance at any stage is a hallmark of coronavirus disease 2019 (COVID-19). Disease severity is associated with increases in peripheral blood cytokines among which interleukin 10 (IL-10) increases particularly early and independent of patient age, which is not seen in active SARS-CoV infection. Here, we consider the known multi-faceted immune regulatory role of IL-10, both in protecting the lung from injury and in defense against infections, as well as its potential cellular source. While the absence of an IL-10 response in SARS is thought to contribute to early deterioration, we suspect IL-10 to protect the lung from early immune-mediated damage and to interfere with viral clearance in COVID-19. This may further both viral spread and poor outcome in many high-risk patients. Identifying the features of the viral genotype, which specifically underlie the different IL-10 dynamics as an etiological endotype and the different viral load kinetics and outcomes as clinical phenotype, may unveil a new immune evasive strategy of SARS-CoV-2.

摘要

严重急性呼吸综合征冠状病毒 2 (SARS-CoV-2) 感染的病理过程使得该病毒对全球健康构成重大威胁,但目前对此了解不足。在任何阶段,病毒清除效率低下都是 2019 年冠状病毒病 (COVID-19) 的标志。疾病的严重程度与外周血细胞因子的增加有关,其中白细胞介素 10 (IL-10) 增加尤其早,且与患者年龄无关,这在活动性 SARS-CoV 感染中并不常见。在这里,我们考虑了已知的 IL-10 的多方面免疫调节作用,既可以保护肺部免受损伤,也可以抵御感染,以及其潜在的细胞来源。虽然 SARS 中缺乏 IL-10 反应被认为是导致早期恶化的原因之一,但我们怀疑 IL-10 可以保护肺部免受早期免疫介导的损伤,并干扰 COVID-19 中的病毒清除。这可能会进一步促进许多高危患者的病毒传播和不良预后。确定病毒基因型的特征,这些特征作为病因学终末型基础,可以解释不同的 IL-10 动力学以及不同的病毒载量动力学和结果作为临床表型,这可能揭示 SARS-CoV-2 的一种新的免疫逃避策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3fc4/7966717/e3542b81fdcb/fimmu-12-602130-g0001.jpg

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