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Mechanisms of Dysregulated Humoral and Cellular Immunity by SARS-CoV-2

机译:SARS-COV-2具有吸诵肱骨和细胞免疫的功能性的机制

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摘要

The current coronavirus disease 2019 (COVID-19) pandemic, a disease caused by severe acute respiratory syndrome corona virus 2 (SARS-CoV-2), was first identified in December 2019 in China, and has led to thousands of mortalities globally each day. While the innate immune response serves as the first line of defense, viral clearance requires activation of adaptive immunity, which employs B and T cells to provide sanitizing immunity. SARS-CoV-2 has a potent arsenal of mechanisms used to counter this adaptive immune response through processes, such as T cells depletion and T cell exhaustion. These phenomena are most often observed in severe SARS-CoV-2 patients, pointing towards a link between T cell function and disease severity. Moreover, neutralizing antibody titers and memory B cell responses may be short lived in many SARS-CoV-2 patients, potentially exposing these patients to re-infection. In this review, we discuss our current understanding of B and T cells immune responses and activity in SARS-CoV-2 pathogenesis.
机译:目前的冠状病毒疾病2019年(Covid-19)大流行,由严重急性呼吸综合征Corona病毒2(SARS-COV-2)引起的疾病,于2019年12月在中国举行,并在全球范围内导致成千上万的死亡。虽然先天免疫反应用作第一道防线,但病毒清除需要激活自适应免疫,其使用B和T细胞来提供消毒免疫力。 SARS-COV-2具有用于通过方法进行计量这种适应性免疫应答的机制有效的机制,例如T细胞耗尽和T细胞耗尽。这些现象通常在严重的SARS-COV-2患者中观察到,指向T细胞功能和疾病严重程度之间的联系。此外,在许多SARS-COV-2患者中,中和抗体滴度和记忆B细胞反应可能短暂寿命,可能将这些患者暴露于重新感染。在本综述中,我们讨论了我们对SARS-COV-2发病机制的B和T细胞免疫应答和活性的了解。

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