Perturbations in the mononuclear phagocyte landscape associated with COVID-19 disease severity
By
Egle Kvedaraite,
Laura Hertwig,
Indranil Sinha,
Andrea Ponzetta,
Ida Hed Myrberg,
Magdalini Lourda,
Majda Dzidic,
Mira Akber,
Jonas Klingström,
Elin Folkesson,
Rao Muvva,
Puran Chen,
Susanna Brighenti,
Anna Norrby-Teglund,
Lars I Eriksson,
Olav Rooyackers,
Soo Aleman,
Kristoffer Stralin,
Hans-Gustaf Ljunggren,
Florent Ginhoux,
Niklas Bjorkstrom,
Jan-Inge Henter,
Mattias Svensson
Posted 31 Aug 2020
medRxiv DOI: 10.1101/2020.08.25.20181404
Monocytes and dendritic cells are crucial mediators of innate and adaptive immune responses during viral infection, but misdirected responses by these cells might contribute to immunopathology. A comprehensive map of the mononuclear phagocyte (MNP) landscape during SARS-CoV-2 infection and concomitant COVID-19 disease is lacking. We performed 25-color flow cytometry-analysis focusing on MNP lineages in SARS-CoV-2 infected patients with moderate and severe COVID-19. While redistribution of monocytes towards intermediate subset and decrease in circulating DCs occurred in response to infection, severe disease associated with appearance of Mo-MDSC-like cells and a higher frequency of pre-DC2. Furthermore, phenotypic alterations in MNPs, and their late precursors, were cell-lineage specific and in select cases associated with severe disease. Finally, unsupervised analysis revealed that the MNP profile, alone, could identify a cluster of COVID-19 non-survivors. This study provides a reference for the MNP response to clinical SARS-CoV-2 infection and unravel myeloid dysregulation associated with severe COVID-19.
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