冠状病毒疾病-2019 感染中的免疫失调范例

O. S. Sahoo, Karthikeyan Pethusamy, A. Nayek, Rashmi Minocha, Ruby Dhar, S. Karmakar
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摘要

2019 年冠状病毒病(COVID-19)大流行导致全球 700-800 万人死亡,造成了前所未有的健康和经济危机。此次疫情影响全球 7 亿人,其严重程度远非人类近代所能匹敌。一项详细调查显示,与严重急性呼吸系统综合征冠状病毒 2(SARS-CoV-2)病毒相比,免疫系统过度活跃导致的损伤才是真正的死亡原因。病毒感染后的细胞因子风暴导致促炎细胞因子激增,导致急性呼吸窘迫综合征(ARDS)和肺损伤。使用抗白细胞介素-6(anti-IL-6)受体单克隆抗体(mAbs;如sarilumab和tocilizumab)和抗IL-6 mAbs(如siltuximab)和/或类固醇方法进行抗炎干预可提供实质性保护并防止死亡,从而暗示炎症在COVID-19中的作用。在这篇综述中,作者总结了 COVID-19 感染中失调的免疫系统,详细研究了病毒-宿主免疫交叉对话,并提出了治疗干预的可能性。
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Paradigm of immune dysregulation in coronavirus disease-2019 infection
The coronavirus disease 2019 (COVID-19) pandemic cost 7–8 million deaths worldwide, creating an unprecedented health and economic crisis. Affecting 700 million people globally, the magnitude of this pandemic is far from anything that humanity has encountered in recent times. A detailed investigation revealed that more than the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) virus, the hyperactive immune system mediated injury as the real cause of mortality. Cytokine storm following viral infection leads to the surge of proinflammatory cytokines resulting in acute respiratory distress syndrome (ARDS) and lung injury. Anti-inflammatory intervention with anti-interleukin-6 (anti-IL-6) receptor monoclonal antibodies (mAbs; e.g., sarilumab and tocilizumab) and anti-IL-6 mAbs (i.e., siltuximab) and/or steroid-based approach leads to substantial protection and prevent death thereby implying the role of inflammation in COVID-19. In this review, the authors have summarized the dysregulated immune system in COVID-19 infection, investigating in detail the virus-host immune cross talks and presenting the possibilities of therapeutic intervention.
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