Anti-SARS-CoV-2 IgG from severely ill COVID-19 patients promotes macrophage hyper-inflammatory responses

Author:

Hoepel WillianneORCID,Chen Hung-Jen,Allahverdiyeva Sona,Manz Xue,Aman Jurjan,Bonta Peter,Brouwer Philip,de Taeye Steven,Caniels Tom,van der Straten Karlijn,Golebski Korneliusz,Griffith Guillermo,Jonkers René,Larsen Mads,Linty Federica,Neele Annette,Nouta Jan,van Baarle Frank,van Drunen Cornelis,Vlaar Alexander,de Bree Godelieve,Sanders Rogier,Willemsen Lisa,Wuhrer Manfred,Bogaard Harm Jan,van Gils Marit,Vidarsson Gestur,de Winther Menno,den Dunnen JeroenORCID,

Abstract

AbstractFor yet unknown reasons, severely ill COVID-19 patients often become critically ill around the time of activation of adaptive immunity. Here, we show that anti-Spike IgG from serum of severely ill COVID-19 patients induces a hyper-inflammatory response by human macrophages, which subsequently breaks pulmonary endothelial barrier integrity and induces microvascular thrombosis. The excessive inflammatory capacity of this anti-Spike IgG is related to glycosylation changes in the IgG Fc tail. Moreover, the hyper-inflammatory response induced by anti-Spike IgG can be specifically counteracted in vitro by use of the active component of fostamatinib, an FDA- and EMA-approved therapeutic small molecule inhibitor of Syk.One sentence summaryAnti-Spike IgG promotes hyper-inflammation.

Publisher

Cold Spring Harbor Laboratory

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