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