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严重的 COVID-19 患者 T 细胞反应低下与病毒持续时间延长和预后不良相关。

Severe T cell hyporeactivity in ventilated COVID-19 patients correlates with prolonged virus persistence and poor outcomes.

机构信息

Department of Nephrology, University Hospital Regensburg, Regensburg, Germany.

Regensburg Center for Interventional Immunology, Regensburg, Germany.

出版信息

Nat Commun. 2021 May 21;12(1):3006. doi: 10.1038/s41467-021-23334-2.

Abstract

Coronavirus disease 2019 (COVID-19) can lead to pneumonia and hyperinflammation. Here we show a sensitive method to measure polyclonal T cell activation by downstream effects on responder cells like basophils, plasmacytoid dendritic cells, monocytes and neutrophils in whole blood. We report a clear T cell hyporeactivity in hospitalized COVID-19 patients that is pronounced in ventilated patients, associated with prolonged virus persistence and reversible with clinical recovery. COVID-19-induced T cell hyporeactivity is T cell extrinsic and caused by plasma components, independent of occasional immunosuppressive medication of the patients. Monocytes respond stronger in males than females and IL-2 partially restores T cell activation. Downstream markers of T cell hyporeactivity are also visible in fresh blood samples of ventilated patients. Based on our data we developed a score to predict fatal outcomes and identify patients that may benefit from strategies to overcome T cell hyporeactivity.

摘要

新型冠状病毒病 2019(COVID-19)可导致肺炎和过度炎症。在这里,我们展示了一种灵敏的方法,通过对全血中的反应细胞(如嗜碱性粒细胞、浆细胞样树突状细胞、单核细胞和中性粒细胞)的下游效应来测量多克隆 T 细胞的活化。我们报告了住院 COVID-19 患者中明显的 T 细胞反应低下,在需要通气的患者中更为明显,与病毒持续存在时间延长有关,并且随着临床康复而可逆。COVID-19 诱导的 T 细胞反应低下是 T 细胞外在的,由血浆成分引起,与患者偶尔接受免疫抑制药物无关。男性的单核细胞反应强于女性,IL-2 部分恢复 T 细胞活化。通气患者的新鲜血液样本中也可见 T 细胞反应低下的下游标志物。基于我们的数据,我们开发了一种评分来预测致命结局,并识别可能受益于克服 T 细胞反应低下的策略的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2222/8140132/f2d66d319f78/41467_2021_23334_Fig1_HTML.jpg

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