The roles of macrophages and monocytes in COVID-19 Severe Respiratory Syndrome.

Publication date: Aug 01, 2025

The global COVID-19 pandemic has highlighted the pivotal role of the immune system in the development of severe respiratory symptoms, termed COVID-19 Severe Respiratory Syndrome (COVID-19-SR). This review aims to dissect the involvement of lung macrophages and monocytes in orchestrating immune responses to SARS-CoV-2, influencing disease severity and outcomes. Initially, we provide an overview of SARS-CoV-2’s invasion process and the body’s primary immune defense mechanisms, including the antibody complement system and cytokine production. We then delve into the roles of the monocyte-macrophage system in mediating hyperinflammation and cytokine storms, discussing how abnormal cytokine and chemokine levels contribute to disease progression. Subsequent sections examine the perturbations and overactivation of the monocyte-macrophage compartment during infection, linking these changes to the observed immune dysregulation in COVID-19 patients. In light of these insights, we explore therapeutic strategies targeting macrophages, such as dexamethasone, antisense lipid nanoparticles(ALN), and inhaled recombinant human granulocyte-macrophage colony-stimulating factor (rh-GM-CSF), which aim to modulate inflammation, suppress viral replication, and enhance viral clearance. Additional potential treatments include GSDMD inhibitors and GPR183 antagonists, which warrant further investigation. This review synthesizes current understanding of the immunopathology underlying COVID-19-SR, proposing macrophage- and monocyte-centered therapeutic avenues and outlining future research priorities essential for advancing clinical management and improving patient outcomes.

Concepts Keywords
Gm COVID-19
Immunopathology Cytokine storm
Long Hyperinflammation
Orchestrating Macrophages
Viral Monocytes
Overactivation

Semantics

Type Source Name
disease MESH COVID-19
disease MESH Syndrome
disease IDO role
pathway REACTOME Immune System
disease IDO process
disease MESH cytokine storms
disease MESH disease progression
disease MESH infection
drug DRUGBANK Dexamethasone
drug DRUGBANK Sargramostim
disease MESH inflammation
pathway KEGG Viral replication
disease MESH Long Covid

Original Article

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