Peripheral T cell lymphopenia in COVID-19: potential mechanisms and impact.

IF 4.1 Q2 IMMUNOLOGY Immunotherapy advances Pub Date : 2021-07-02 eCollection Date: 2021-01-01 DOI:10.1093/immadv/ltab015
Sifan Zhang, Becca Asquith, Richard Szydlo, John S Tregoning, Katrina M Pollock
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引用次数: 11

Abstract

Immunopathogenesis involving T lymphocytes, which play a key role in defence against viral infection, could contribute to the spectrum of COVID-19 disease and provide an avenue for treatment. To address this question, a review of clinical observational studies and autopsy data in English and Chinese languages was conducted with a search of registered clinical trials. Peripheral lymphopenia affecting CD4 and CD8 T cells was a striking feature of severe COVID-19 compared with non-severe disease. Autopsy data demonstrated infiltration of T cells into organs, particularly the lung. Seventy-four clinical trials are on-going that could target T cell-related pathogenesis, particularly IL-6 pathways. SARS-CoV-2 infection interrupts T cell circulation in patients with severe COVID-19. This could be due to redistribution of T cells into infected organs, activation induced exhaustion, apoptosis, or pyroptosis. Measuring T cell dynamics during COVID-19 will inform clinical risk-stratification of hospitalised patients and could identify those who would benefit most from treatments that target T cells.

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COVID-19外周血T细胞淋巴减少:潜在机制和影响
涉及T淋巴细胞的免疫发病机制在防御病毒感染中发挥关键作用,可能有助于COVID-19疾病的范围并提供治疗途径。为了解决这个问题,我们对中英文临床观察研究和尸检数据进行了回顾,并检索了已注册的临床试验。与非严重疾病相比,影响CD4和CD8 T细胞的外周血淋巴细胞减少是重症COVID-19的一个显著特征。尸检数据显示T细胞浸润到器官,特别是肺。74项临床试验正在进行中,可以针对T细胞相关的发病机制,特别是IL-6途径。SARS-CoV-2感染阻断了重症COVID-19患者的T细胞循环。这可能是由于T细胞重新分配到受感染的器官,激活诱导的衰竭,凋亡或焦亡。在COVID-19期间测量T细胞动力学将为住院患者的临床风险分层提供信息,并可以确定哪些人将从靶向T细胞的治疗中获益最多。
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7 weeks
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