Evidence map›Paper›PMID 40959094›Full record

ArticleFrontiers in immunology2025

Rational design of an epitope-centric vaccine against

Santhosh Mudipalli Elavarasu, Sasikumar K

Abstract read
In one paragraph

Article in Frontiers in immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

2 authors.

Santhosh Mudipalli ElavarasuDepartment of Integrative Biology, School of Biosciences and Technology, Vellore Institute of Technology (VIT), Vellore, Tamil Nadu, India.
Sasikumar KDepartment of Sensor and Biomedical Technology, School of Electronics Engineering, Vellore Institute of Technology (VIT), Vellore, Tamil Nadu, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: As a highly adaptable opportunistic pathogen, Methods: A pangenome analysis of Results: Our pangenome analysis identified highly conserved core genes, including LptF, which proved crucial for bacterial virulence. A multi-epitope peptide vaccine was designed using the most immunogenic B-cell and T-cell epitopes derived from LptF. Studies using molecular docking and dynamic simulation have shown stable interactions between the vaccine and TLRs, with the POA_V_RS09 construct exhibiting the highest stability. Codon optimization indicated high expression efficiency in Discussion: The POA_V_RS09 vaccine candidate exhibited excellent stability, immunogenic potential, and expression efficiency, making it a promising candidate for combating

Indexed as

Epitopes, B-LymphocyteEpitopes, T-LymphocytePseudomonas aeruginosaPseudomonas InfectionsPseudomonas VaccinesComputational BiologyGenome, BacterialHumansImmunogenicity, VaccineImmunoinformaticsMolecular Docking SimulationMolecular Dynamics SimulationVaccine DevelopmentVaccines, SubunitEpitopes, B-LymphocyteEpitopes, T-LymphocytePseudomonas VaccinesVaccines, Subunitepitope-based vaccineimmune simulationimmunoinformaticsmolecular dockingpangenome analysisPseudomonas aeruginosa

Identifiers

PMID40959094
PMCPMC12434008

What OpenQuestion holds

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LicenceCC BY
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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.