4.6 Article

Mechanistic Understanding of the Olfactory Neuroepithelium Involvement Leading to Short-Term Anosmia in COVID-19 Using the Adverse Outcome Pathway Framework

Journal

CELLS
Volume 11, Issue 19, Pages -

Publisher

MDPI
DOI: 10.3390/cells11193027

Keywords

SARS-CoV-2 infection; COVID-19; anosmia; olfactory neuroepithelium; AOP

Categories

Funding

  1. Academy of Finland [335524]
  2. University of Eastern Finland
  3. European Commission, Joint Research Centre (JRC), Ispra, Italy
  4. Academy of Finland (AKA) [335524, 335524] Funding Source: Academy of Finland (AKA)

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Loss of the sense of smell is a symptom of COVID-19, with most patients recovering within a few weeks, while others experience persistent anosmia. This study aims to evaluate the mechanisms leading to short-term anosmia following SARS-CoV-2 infection. Using an adverse outcome pathway (AOP) framework, the study proposes a sequence of measurable key events that contribute to short-term anosmia, providing insights for further research and therapeutic intervention.
Loss of the sense of smell (anosmia) has been included as a COVID-19 symptom by the World Health Organization. The majority of patients recover the sense of smell within a few weeks postinfection (short-term anosmia), while others report persistent anosmia. Several studies have investigated the mechanisms leading to anosmia in COVID-19; however, the evidence is scattered, and the mechanisms remain poorly understood. Based on a comprehensive review of the literature, we aim here to evaluate the current knowledge and uncertainties regarding the mechanisms leading to short-term anosmia following SARS-CoV-2 infection. We applied an adverse outcome pathway (AOP) framework, well established in toxicology, to propose a sequence of measurable key events (KEs) leading to short-term anosmia in COVID-19. Those KEs are (1) SARS-CoV-2 Spike proteins binding to ACE-2 expressed by the sustentacular (SUS) cells in the olfactory epithelium (OE); (2) viral entry into SUS cells; (3) viral replication in the SUS cells; (4) SUS cell death; (5) damage to the olfactory sensory neurons and the olfactory epithelium (OE). This AOP-aligned approach allows for the identification of gaps where more research should be conducted and where therapeutic intervention could act. Finally, this AOP gives a frame to explain several disease features and can be linked to specific factors that lead to interindividual differences in response to SARS-CoV-2 infection.

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