Heliyon
Volume 9, Issue 2, February 2023, e13285
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Review article
Insight into SARS-CoV-2 Omicron variant immune escape possibility and variant independent potential therapeutic opportunities

https://doi.org/10.1016/j.heliyon.2023.e13285Get rights and content
Under a Creative Commons license
open access

Highlights

  • The Omicron is the most highly mutated variant compared to other variants of SARS-CoV-2.

  • Omicron is highly infectious and spreads rapidly, but causes less severe disease than other variants.

  • Omicron is now a dominant variant worldwide and is predicted to be able to escape immunity.

  • Humoral immunity from vaccines was found to reduced, but T cell immunity was still protective against Omicron infection.

  • Drugs targeting oxidative stress, cytokines, and viral replicase exhibit beneficial effects in Omicron-infected patients.

Abstract

The Omicron, the latest variant of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2), was first detected in November 2021 in Botswana, South Africa. Compared to other variants of SARS-CoV-2, the Omicron is the most highly mutated, with 50 mutations throughout the genome, most of which are in the spike (S) protein. These mutations may help the Omicron to evade host immunity against the vaccine. Epidemiological studies suggest that Omicron is highly infectious and spreads rapidly, but causes significantly less severe disease than the wild‐type strain and the other variants of SARS-CoV-2. With the increased transmissibility and a higher rate of re-infection, Omicron has now become a dominant variant worldwide and is predicted to be able to evade vaccine-induced immunity. Several clinical studies using plasma samples from individuals receiving two doses of US Food and Drugs Administration (FDA)-approved COVID-19 vaccines have shown reduced humoral immune response against Omicron infection, but T cell-mediated immunity was well preserved. In fact, T cell-mediated immunity protects against severe disease, and thus the disease caused by Omicron remains mild. In this review, I surveyed the current status of Omicron variant mutations and mechanisms of immune response in the context of immune escape from COVID-19 vaccines. I also discuss the potential implications of therapeutic opportunities that are independent of SARS-CoV-2 variants, including Omicron. A better understanding of vaccine-induced immune responses and variant-independent therapeutic interventions that include potent antiviral, antioxidant, and anti-cytokine activities may pave the way to reducing Omicron-related COVID-19 complications, severity, and mortality. Collectively, these insights point to potential research gaps and will aid in the development of new-generation COVID-19 vaccines and antiviral drugs to combat Omicron, its sublineages, or upcoming new variants of SARS-CoV-2.

Keywords

Omicron
Immune escape
Variants
Humoral immunity
T cell immunity

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