Coronavirus disease 2019 induces multi-lineage, morphologic changes in peripheral blood cells.
Florian LükeEvelyn OrsóJana KirstenHendrik PoeckMatthias GrubeDaniel WolffRalph BurkhardtDirk LunzMatthias LubnowBarbara SchmidtFlorian HitzenbichlerFrank HansesBernd SalzbergerMatthias EvertWolfgang HerrChristoph BrochhausenTobias PukropAlbrecht ReichleDaniel HeudoblerPublished in: EJHaem (2020)
The clinical course of coronavirus disease 2019 (COVID-19) varies from mild symptoms to acute respiratory distress syndrome, hyperinflammation, and coagulation disorder. The hematopoietic system plays a critical role in the observed hyperinflammation, particularly in severely ill patients. We conducted a prospective diagnostic study performing a blood differential analyzing morphologic changes in peripheral blood of COVID-19 patients. COVID-19 associated morphologic changes were defined in a training cohort and subsequently validated in a second cohort (n = 45). Morphologic aberrations were further analyzed by electron microscopy (EM) and flow cytometry of lymphocytes was performed. We included 45 COVID-19 patients in our study (median age 58 years; 82% on intensive care unit). The blood differential showed a specific pattern of pronounced multi-lineage aberrations in lymphocytes (80%) and monocytes (91%) of patients. Overall, 84%, 98%, and 98% exhibited aberrations in granulopoiesis, erythropoiesis, and thrombopoiesis, respectively. Electron microscopy revealed the ultrastructural equivalents of the observed changes and confirmed the multi-lineage aberrations already seen by light microscopy. The morphologic pattern caused by COVID-19 is characteristic and underlines the serious perturbation of the hematopoietic system. We defined a hematologic COVID-19 pattern to facilitate further independent diagnostic analysis and to investigate the impact on the hematologic system during the clinical course of COVID-19 patients.
Keyphrases
- coronavirus disease
- peripheral blood
- sars cov
- electron microscopy
- acute respiratory distress syndrome
- intensive care unit
- respiratory syndrome coronavirus
- end stage renal disease
- ejection fraction
- copy number
- single cell
- newly diagnosed
- chronic kidney disease
- flow cytometry
- bone marrow
- mechanical ventilation
- prognostic factors
- extracorporeal membrane oxygenation
- patient reported outcomes
- high resolution
- oxidative stress
- dendritic cells
- cell proliferation
- single molecule
- depressive symptoms
- cell death
- optical coherence tomography
- gene expression
- data analysis