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Updated: Oct 19, 2025

Author Spotlight: Advancements in Multiplex Detection of Respiratory Viruses
Published on: November 10, 2023
A scoping review of the pathophysiology of COVID-19
Paul E Marik1,2, Jose Iglesias3,2, Joseph Varon4,2
1Division of Pulmonary and Critical Care Medicine, 6040Eastern Virginia Medical School, Norfolk, VA, USA.
Insights
Severe COVID-19 involves complex pathogenesis, including pulmonary inflammation, endothelialitis, and a procoagulant state. Understanding these mechanisms is crucial for developing effective treatments and prevention strategies for coronavirus disease 2019.
Area of Science:
- Pathology
- Immunology
- Virology
Background:
- COVID-19 presents as a complex and heterogeneous disease.
- A comprehensive understanding of COVID-19 pathogenesis is currently lacking.
- Effective prophylactic and treatment strategies require a deep understanding of disease mechanisms.
Purpose of the Study:
- To provide a clinical overview of the major pathogenetic mechanisms leading to severe COVID-19.
- To synthesize findings from clinical, proteomic, genomic, and autopsy studies.
- To elucidate the multifactorial nature of severe COVID-19.
Main Methods:
- Review of clinical data.
- Analysis of proteomic and genomic studies.
- Examination of autopsy findings.
Main Results:
- Severe COVID-19 is characterized by pulmonary macrophage activation syndrome with uncontrolled inflammation.
- Complement-mediated endothelialitis and a procoagulant state with thrombotic microangiopathy are key features.
- Platelet activation, mast cell degranulation, and auto-antibodies contribute to hyper-inflammation and end-organ damage.
Conclusions:
- Severe COVID-19 results from the interplay of inflammation, endothelial damage, and thrombosis.
- Identifying these pathogenetic pathways is essential for therapeutic development.
- Further research into these mechanisms will guide the management of severe coronavirus disease 2019.
Abstract:
COVID-19 is a highly heterogeneous and complex medical disorder; indeed, severe COVID-19 is probably amongst the most complex of medical conditions known to medical science. While enormous strides have been made in understanding the molecular pathways involved in patients infected with coronaviruses an overarching and comprehensive understanding of the pathogenesis of COVID-19 is lacking. Such an understanding is essential in the formulation of effective prophylactic and treatment strategies. Based on clinical, proteomic, and genomic studies as well as autopsy data severe COVID-19 disease can be considered to be the connection of three basic pathologic processes, namely a pulmonary macrophage activation syndrome with uncontrolled inflammation, a complement-mediated endothelialitis together with a procoagulant state with a thrombotic microangiopathy. In addition, platelet activation with the release of serotonin and the activation and degranulation of mast cells contributes to the hyper-inflammatory state. Auto-antibodies have been demonstrated in a large number of hospitalized patients which adds to the end-organ damage and pro-thrombotic state. This paper provides a clinical overview of the major pathogenetic mechanism leading to severe COVID-19 disease.
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