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Published on: February 16, 2022
Anti-IgE monoclonal antibodies as potential treatment in COVID-19
Ahmad Reza Farmani1,2,3, Forough Mahdavinezhad4, Rohollah Moslemi5
1Tissue Engineering and Applied Cell Sciences Department, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.
Insights
Immunoglobulin E (IgE) contributes to severe COVID-19 by exacerbating inflammation. Blocking IgE with drugs like omalizumab may reduce disease severity and duration, offering a potential immunotherapy.
Area of Science:
- Immunology
- Virology
- Pharmacology
Background:
- Coronavirus disease 2019 (COVID-19) can cause irreversible organ damage due to a hyperinflammatory immune response, termed cytokine storm.
- Immunoglobulin E (IgE) is implicated in hypersensitivity, respiratory infections, and mast cell activation, potentially worsening COVID-19 outcomes.
- IgE negatively correlates with Interferon-alpha (IFN-α) production, impairing the immune response against viral infections.
Purpose of the Study:
- To explore the role of Immunoglobulin E (IgE) in the pathogenesis of COVID-19.
- To investigate the potential of anti-IgE therapy, specifically omalizumab, as an immunotherapy for COVID-19.
Main Methods:
- Review of existing literature on COVID-19, immune responses, IgE, and anti-IgE therapies.
- Analysis of the mechanisms by which IgE influences viral infections and inflammation.
- Evaluation of omalizumab's effects on IgE, inflammatory cells, and COVID-19 severity.
Main Results:
- COVID-19 is characterized by a cytokine storm, a severe immune overreaction damaging multiple organs.
- IgE plays a significant role in hypersensitivity and respiratory infections, potentially exacerbating COVID-19.
- Omalizumab, an anti-IgE drug, has shown potential in reducing COVID-19 severity and duration by inhibiting IgE and inflammatory cells like neutrophils.
Conclusions:
- Blockade of IgE represents a promising therapeutic strategy for managing COVID-19.
- Anti-IgE agents like omalizumab may serve as effective immunotherapies for COVID-19 patients.
- Targeting IgE could mitigate the hyperinflammatory response and organ damage associated with severe COVID-19.
Abstract:
Coronavirus disease 2019 (COVID-19) is associated with irreversible effects on vital organs, especially the respiratory and cardiac systems. While the immune system plays a key role in the survival of patients to viral infections, in COVID-19, there is a hyperinflammatory immune response evoked by all the immune cells, such as neutrophils, monocytes, and includes release of various cytokines, resulting in an exaggerated immune response, named cytokine storm. This severe, dysregulated immune response causes multi-organ damage, which eventually leads to high mortality. One of the most important components of hypersensitivity is immunoglobulin E (IgE), which plays a major role in susceptibility to respiratory infections and can lead to the activation of mast cells. There is also a negative association between IgE and IFN-α, which can reduce Toll-like receptor (TLR) nine receptor expression and TLR-7 signaling to disrupt IFN production. Moreover, anti-IgE drugs such as omalizumab reduces the severity and duration of COVID-19. In addition to its anti-IgE effect, omalizumab inhibits inflammatory cells such as neutrophils. Hence, blockade of IgE may have clinical utility as an immunotherapy for COVID-19.
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