| Literature DB >> 32870529 |
Benedetta Peruzzi1, Sara Bencini1, Manuela Capone2, Alessio Mazzoni2, Laura Maggi2, Lorenzo Salvati2, Anna Vanni2, Chiara Orazzini1, Carlo Nozzoli3, Alessandro Morettini4, Loredana Poggesi2,5, Filippo Pieralli6, Adriano Peris7, Alessandro Bartoloni2,8, Alessandro Maria Vannucchi2,9, Francesco Liotta2,10, Roberto Caporale1, Lorenzo Cosmi2,10, Francesco Annunziato1,2.
Abstract
SARS-CoV-2 is responsible for a new infectious disease (COVID-19) in which individuals can either remain asymptomatic or progress from mild to severe clinical conditions including acute respiratory distress syndrome and multiple organ failure. The immune mechanisms that potentially orchestrate the pathology in SARS-CoV-2 infection are complex and only partially understood. There is still paucity of data on the features of myeloid cells involved in this viral infection. For this reason, we investigated the different activation status profiles and the subset distribution of myeloid cells and their correlation with disease progression in 40 COVID-19 patients at different stages of disease. COVID-19 patients showed a decrease in the absolute number of plasmacytoid and myeloid dendritic cells, different subset distribution of monocytes and different activation patterns of both monocytes and neutrophils, coupled to a significant reduction of HLA-DR monocyte levels. We found that some of these alterations are typical of all COVID-19 patients, while some others vary at different stages of the disease and correlate with biochemical parameters of inflammation. Collectively, these data suggest that not only the lymphoid, but also the myeloid compartment, is severely affected by SARS-CoV-2 infection.Entities:
Mesh:
Year: 2020 PMID: 32870529 PMCID: PMC7692244 DOI: 10.1111/imm.13254
Source DB: PubMed Journal: Immunology ISSN: 0019-2805 Impact factor: 7.397