SARS-CoV-2: A Glance at the Innate Immune Response Elicited by Infection and Vaccination.
Nicola ManfriniSamuele NotarbartoloRenata GrifantiniElisa PescePublished in: Antibodies (Basel, Switzerland) (2024)
The COVID-19 pandemic caused by Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) has led to almost seven million deaths worldwide. SARS-CoV-2 causes infection through respiratory transmission and can occur either without any symptoms or with clinical manifestations which can be mild, severe or, in some cases, even fatal. Innate immunity provides the initial defense against the virus by sensing pathogen-associated molecular patterns and triggering signaling pathways that activate the antiviral and inflammatory responses, which limit viral replication and help the identification and removal of infected cells. However, temporally dysregulated and excessive activation of the innate immune response is deleterious for the host and associates with severe COVID-19. In addition to its defensive role, innate immunity is pivotal in priming the adaptive immune response and polarizing its effector function. This capacity is relevant in the context of both SARS-CoV-2 natural infection and COVID-19 vaccination. Here, we provide an overview of the current knowledge of the innate immune responses to SARS-CoV-2 infection and vaccination.
Keyphrases
- immune response
- sars cov
- respiratory syndrome coronavirus
- dendritic cells
- coronavirus disease
- toll like receptor
- induced apoptosis
- signaling pathway
- healthcare
- pi k akt
- cell cycle arrest
- epithelial mesenchymal transition
- weight gain
- endoplasmic reticulum stress
- cell proliferation
- candida albicans
- body mass index
- sleep quality
- drug induced
- weight loss