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Published on: March 9, 2018
Insight into Covid Associated Mucormycosis: A Prospective Study
Avinash-Shekhar Jaiswal1, Aanchal Kakkar2, Kavneet Kaur2
1Department of Otorhinolaryngology and Head & Neck Surgery, All India Institute of Medical Sciences, New Delhi, India.
Elevated TMPRSS2 receptors in COVID-19-associated mucormycosis patients may explain increased susceptibility. ACE2 receptor expression remained unchanged, suggesting TMPRSS2 plays a key role in this co-infection.
Area of Science:
- Infectious Diseases
- Otolaryngology
- Virology
Background:
- Rhino-orbito-cerebral mucormycosis cases surged during the COVID-19 pandemic.
- Both COVID-19 and mucormycosis share the nasal mucosa as an entry point, prompting investigation into shared receptor roles.
- Understanding these molecular interactions is crucial for managing co-infections.
Purpose of the Study:
- To compare the expression of ACE2 and TMPRSS2 receptors in nasal and paranasal sinus tissues.
- To analyze receptor expression in patients with COVID-19-associated mucormycosis (CAM), COVID-19-negative mucormycosis (CNM), and healthy controls.
Main Methods:
- Prospective study involving patients undergoing surgical management for CAM, CNM, and healthy individuals.
- Immunohistochemistry used to detect ACE2 and TMPRSS2 receptor presence in sino-nasal tissues.
- Statistical comparison of receptor levels across the three study groups.
Main Results:
- ACE2 receptor positivity was observed only in apical cilia, with no significant differences among groups (p=0.6).
- TMPRSS2 receptors were found in the cytoplasm, nucleus, epithelium, and submucosal glands.
- TMPRSS2 expression was significantly higher in CAM patients compared to CNM (p=0.009) and healthy individuals (p=0.002).
Conclusions:
- TMPRSS2 receptor expression is elevated in patients with COVID-19-associated mucormycosis.
- ACE2 receptor expression did not significantly change between groups.
- Elevated TMPRSS2 may contribute to heightened susceptibility to SARS-CoV-2 and subsequent Mucorales co-infection.
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