Evidence map›Paper›PMID 40358996›Full record

ArticleThe Journal of general virology2025

The impact of pre-existing immunity on the emergence of within-host immune-escape mutations in Omicron lineages.

Muna N Ahmed, Ummay Salma Abu Habib, Abdallah M Abdallah, Mohamed M Emara, Arnab Pain, Asmaa A Althani, Gheyath K Nasrallah, Hadi M Yassine, Hebah A Al-Khatib

Abstract read
In one paragraph

Article in The Journal of general virology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

9 authors.

Muna N AhmedBiomedical Research Center, QU Health, Qatar University, Doha, P.O. 2713, Qatar.
Ummay Salma Abu HabibCollege of Health Sciences, QU Health, Qatar University, Doha, P.O. 2713, Qatar.
Abdallah M AbdallahCollege of Medicine, QU Health, Qatar University, Doha, P.O. 2713, Qatar.
Mohamed M EmaraCollege of Medicine, QU Health, Qatar University, Doha, P.O. 2713, Qatar.
Arnab PainPathogen Genomics Laboratory, Bioscience Program, Biological and Environmental Science and Engineering (BESE), King Abdullah University of Science and Technology (KAUST), Thuwal, 23955-6900, Saudi Arabia.
Asmaa A AlthaniBiomedical Research Center, QU Health, Qatar University, Doha, P.O. 2713, Qatar.
Gheyath K NasrallahCollege of Health Sciences, QU Health, Qatar University, Doha, P.O. 2713, Qatar.
Hadi M YassineBiomedical Research Center, QU Health, Qatar University, Doha, P.O. 2713, Qatar.
Hebah A Al-KhatibBiomedical Research Center, QU Health, Qatar University, Doha, P.O. 2713, Qatar.

Funding

Wellcome Trust
6 · The paper itself

Abstract

The Omicron variant of SARS-CoV-2 circulating amongst highly immunized populations is anticipated to induce immunological pressures, potentially compromising existing immunity. This study investigates vaccine-induced immunity's impact on within-host diversity of Omicron variants and evaluates sub-consensus mutations at spike protein antigenic sites. Next-generation sequencing assessed the within-host diversity of 728 Omicron-positive samples (421 vaccinated; 307 unvaccinated). Quantitative analysis revealed limited vaccine impact, regardless of lineage, vaccine type or doses. Non-lineage mutations (39, 33 and 25 in BA.2*, BA.4* and BA.5* lineages, respectively) were detected, some showing higher incidence in vaccinated individuals. Six mutations detected at sub-consensus levels at antigenic sites suggest increased immune pressure on the spike protein in vaccinated individuals. Four high-prevalence antigenic mutations, absent from global GISAID sequences, were identified. Although within-host diversity did not significantly differ between vaccination statuses, detected mutations suggest that vaccine-induced immunity may influence within-host mutation patterns.

Indexed as

COVID-19COVID-19 VaccinesImmune EvasionSARS-CoV-2Spike Glycoprotein, CoronavirusHigh-Throughput Nucleotide SequencingHumansMutationVaccinationCOVID-19 VaccinesSpike Glycoprotein, Coronavirusspike protein, SARS-CoV-2immune pressurequasispeciesSARS-CoV-2vaccinationvirus evolution

Identifiers

PMID40358996
PMCPMC12075854

What OpenQuestion holds

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LicenceCC BY
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.