Evidence map›Paper›PMID 38726782›Full record

ReviewCurrent drug targets2024

Comprehensive Analysis of Omicron Subvariants: EG.5 Rise, Vaccination Strategies, and Global Impact.

Debayan Sil, Shreastha Gautam, Shubhi Saxena, Sachin Joshi, Dinesh Kumar, Astha Mehta, Priya Jindal, Subhi Sharma, Prachi Pandey, Diksha and 1 more

Abstract readReview
PubMed Publisher
In one paragraph

Review in Current drug targets, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

  1. Article
  2. Article
  3. COVID-19-Where Are We Now.Current medicinal chemistry · 2025
    Article
  4. Article
  5. Article
  6. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Debayan SilDepartment of Quality Assurance, ISF College of Pharmacy, Moga, Punjab, 142001, India.
Shreastha GautamDepartment of Quality Assurance, ISF College of Pharmacy, Moga, Punjab, 142001, India.
Shubhi SaxenaDepartment of Quality Assurance, ISF College of Pharmacy, Moga, Punjab, 142001, India.
Sachin JoshiDepartment of Quality Assurance, ISF College of Pharmacy, Moga, Punjab, 142001, India.
Dinesh KumarDepartment of Quality Assurance, ISF College of Pharmacy, Moga, Punjab, 142001, India.
Astha MehtaDepartment of Quality Assurance, ISF College of Pharmacy, Moga, Punjab, 142001, India.
Priya JindalDepartment of Quality Assurance, ISF College of Pharmacy, Moga, Punjab, 142001, India.
Subhi SharmaDepartment of Quality Assurance, ISF College of Pharmacy, Moga, Punjab, 142001, India.
Prachi PandeyDepartment of Quality Assurance, ISF College of Pharmacy, Moga, Punjab, 142001, India.
DikshaDepartment of Quality Assurance, ISF College of Pharmacy, Moga, Punjab, 142001, India.
Amandeep SinghDepartment of Pharmaceutics, ISF College of Pharmacy, Moga, Punjab, 142001, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The emergence of new variants of the SARS-CoV-2 virus during the COVID-19 pandemic has prompted significant developments in the understanding, monitoring, and response to these strains. This comprehensive review focuses on two prominent variants of interest (VoI), XBB. 1.5 (Kraken) and XBB.1.16 ("Arcturus"), along with seven variants under observation (VuM), including EG.5. The World Health Organization (WHO) identified these variants in July 2023, highlighting EG.5's noteworthy rise in prevalence. EG.5, also known as "Eris," has exhibited an increased effective reproductive rate, prompting concerns about its contagiousness and immune evasion capabilities. With an altered spike protein in the Receptor-Binding Domain (RBD), EG.5 shares similarities with XBB.1.5 but surpasses it in prevalence, constituting 20% of COVID-19 cases in the United States by late August. EG.5's subvariant, EG.5.1, poses challenges with mutations like Q52H and F456L, contributing to its ability to bypass neutralizing antibodies. The global distribution of SARS-CoV-2 variants presents a dynamic landscape, with XBB.1.16 and other strains gaining prominence. The advent of the BA.2.86 variant further complicates the scenario, with its notable spread in regions lacking robust viral surveillance. A thorough analysis of mutations reveals the evolving nature of the Omicron variant, with distinct amino acid changes characterizing XBB.1.5, XBB.1.16, and EG.5. The WHO designates EG.5 as a "variant of interest" due to its increased contagiousness and potential immune evasion, emphasizing the need for vigilant monitoring. The risk assessment of EG.5 underscores its rapid development and growing prevalence globally. While booster vaccines targeting XBB.1.5 are in development, antiviral medications like nirmatrelvir/ritonavir (Paxlovid) continue to exhibit efficacy. In the context of the evolving variants, the FDA has granted emergency use authorization for updated COVID-19 vaccines targeting circulating strains, reflecting the adaptability of vaccination strategies to address emerging challenges. This comprehensive overview provides a nuanced understanding of the diverse Omicron subvariants, their global impact, and the ongoing efforts to combat their spread through vaccination and therapeutic interventions.

Indexed as

COVID-19COVID-19 VaccinesSARS-CoV-2Global HealthHumansImmune EvasionSpike Glycoprotein, CoronavirusVaccinationCOVID-19 VaccinesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2COVID-19 pandemicEG.5global impactOmicron subvariantsrisk assessment.vaccine developmentXBB.1.16XBB.1.5

Identifiers

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.