Evidence map›Paper›PMID 41663438›Full record

ArticleScientific reports2026

AntiPan: a genome-informed in silico pipeline for advancing subunit vaccine discovery against Staphylococcus aureus.

Mostafa S Ibrahim, Jala A Fahmy, Mohamed A Helal, Fady T Hakim, Lydia R Sidarous, Nayera E Attallah, Sherif Abouelhadid, Mohamed Elhadidy, Eman Badr

Abstract read
In one paragraph

Article in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
–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 synthesis or guideline pooled it.

  1. Pooled it
  2. Frontiers in bioinformatics · 2026
    Review
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.

Mostafa S Ibrahim *Center for Genomics, Helmy Institute for Medical Sciences, Zewail City of Science and Technology, Giza, Egypt.
Jala A Fahmy *Center for Genomics, Helmy Institute for Medical Sciences, Zewail City of Science and Technology, Giza, Egypt.
Mohamed A HelalBiomedical Sciences Program, University of Science and Technology, Zewail City of Science and Technology, Giza, Egypt.
Fady T HakimBiomedical Sciences Program, University of Science and Technology, Zewail City of Science and Technology, Giza, Egypt.
Lydia R SidarousBiomedical Sciences Program, University of Science and Technology, Zewail City of Science and Technology, Giza, Egypt.
Nayera E AttallahCenter for Genomics, Helmy Institute for Medical Sciences, Zewail City of Science and Technology, Giza, Egypt.
Sherif AbouelhadidSchool of Biotechnology, Nile University, Giza, Egypt. sabouelhadid@nu.edu.eg.
Mohamed ElhadidyCenter for Genomics, Helmy Institute for Medical Sciences, Zewail City of Science and Technology, Giza, Egypt. melhadidy@zewailcity.edu.eg.
Eman BadrBiomedical Sciences Program, University of Science and Technology, Zewail City of Science and Technology, Giza, Egypt. emostafa@zewailcity.edu.eg.

Funding

Bactivac Catalyst Pump-Priming Projects grant BVNCP8-10Science, Technology & Innovation Funding Authority (STDF) One Health Research and Innovation Grant (OHRIG) 48072
6 · The paper itself

Abstract

Staphylococcus aureus (S. aureus) remains a major global health threat due to its multidrug resistance and immune evasion mechanisms. Despite numerous vaccine trials, no licensed vaccine is currently available for human use. Existing reverse vaccinology pipelines often neglect key host-pathogen immune interactions or rely on limited toolsets. This study introduces AntiPan, an enhanced in silico pipeline for identifying high-potential protein antigens for subunit vaccine design. AntiPan integrates five modules: pan-genome analysis, reverse vaccinology filters, protein assessment, immunoinformatics, and Toll-like receptors binding evaluation, while accounting for genomic diversity and immune evasion mechanisms. Using the genome of S. aureus isolated in Egypt, AntiPan identified 29 protective antigen candidates (PACs) implicated in host invasion, nutrient acquisition, and immune evasion. Ten PACs were shortlisted for future experimental validation, including IsdC, EbpS, SspB, EssA, TagH, SirA, EsxA, AmiA, HlgC, and HlgB. Molecular docking demonstrated that IsdC, AmiA, and TagH bind strongly and complementarily to the TLR1/TLR2 and TLR4/MD2 complexes, making them top vaccine candidates. Molecular dynamics simulations and MHC-epitope docking results further confirmed the immunogenicity potential of the top-ranked PACs. AntiPan is a command-line tool that provides an accessible, reproducible, and scalable platform for discovering bacterial vaccine targets. It applies to multidrug-resistant pathogens and is publicly available at: https://github.com/ComputationalBiologyLab/AntiPan .

Indexed as

Staphylococcal InfectionsStaphylococcal VaccinesStaphylococcus aureusVaccines, SubunitAntigens, BacterialComputer SimulationGenome, BacterialHumansImmunoinformaticsMolecular Docking SimulationProtein Subunit VaccinesReverse VaccinologyToll-Like ReceptorsVaccine DevelopmentAntigens, BacterialProtein Subunit VaccinesStaphylococcal VaccinesToll-Like ReceptorsVaccines, SubunitAntimicrobial resistanceImmunoinformaticsMolecular dockingReverse vaccinologySubunit vaccineToll-like receptors

Identifiers

PMID41663438
PMCPMC12887025

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.