Department of Infectious Diseases and Immunology, Alder Hey Children's NHS Foundation Trust Hospital, Liverpool, UK.
Department of Women's & Children's Health, Institute of Translational Medicine, University of Liverpool, Liverpool, UK.
Clin Immunol. 2020 Jun;215:108448. doi: 10.1016/j.clim.2020.108448. Epub 2020 Apr 27.
The novel coronavirus SARS-CoV2 causes COVID-19, a pandemic threatening millions. As protective immunity does not exist in humans and the virus is capable of escaping innate immune responses, it can proliferate, unhindered, in primarily infected tissues. Subsequent cell death results in the release of virus particles and intracellular components to the extracellular space, which result in immune cell recruitment, the generation of immune complexes and associated damage. Infection of monocytes/macrophages and/or recruitment of uninfected immune cells can result in massive inflammatory responses later in the disease. Uncontrolled production of pro-inflammatory mediators contributes to ARDS and cytokine storm syndrome. Antiviral agents and immune modulating treatments are currently being trialled. Understanding immune evasion strategies of SARS-CoV2 and the resulting delayed massive immune response will result in the identification of biomarkers that predict outcomes as well as phenotype and disease stage specific treatments that will likely include both antiviral and immune modulating agents.
新型冠状病毒 SARS-CoV2 引起的 COVID-19 是一种威胁数百万人的大流行疾病。由于人类没有保护性免疫,并且该病毒能够逃避先天免疫反应,因此它可以在主要感染组织中不受阻碍地增殖。随后的细胞死亡导致病毒颗粒和细胞内成分释放到细胞外空间,从而导致免疫细胞募集、免疫复合物的产生和相关损伤。单核细胞/巨噬细胞的感染和/或未感染免疫细胞的募集可导致疾病后期发生大规模炎症反应。促炎介质的失控产生导致急性呼吸窘迫综合征和细胞因子风暴综合征。目前正在试验抗病毒药物和免疫调节治疗。了解 SARS-CoV2 的免疫逃逸策略以及由此导致的延迟的大规模免疫反应,将有助于确定预测结果的生物标志物,以及针对表型和疾病阶段的特异性治疗方法,这些方法可能包括抗病毒和免疫调节药物。