Evidence map›Paper›PMID 42370218›Full record

ReviewInfection and drug resistance2026

Antimicrobial Peptides Against Antimicrobial-Resistant Bacteria: Focus on Machine Learning.

Hamed Tahmasebi, Mohammad Reza Arabestani

Abstract readReview
In one paragraph

Review in Infection and drug resistance, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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.

Hamed TahmasebiSchool of Medicine, Shahroud University of Medical Sciences, Shahroud, Iran.ORCID 0000-0002-9257-4479
Mohammad Reza ArabestaniDepartment of Microbiology, School of Medicine, Hamadan University of Medical Sciences, Hamadan, Iran.ORCID 0000-0001-9991-8193

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antimicrobial resistance (AMR) represents a pressing public health threat of the 21st century, with an estimated ten million deaths annually from drug-resistant infections by 2050. Diminishing pipelines and the accelerating emergence of multidrug-resistant pathogens make the development of novel antibacterials more urgent than ever. Antimicrobial peptides (AMPs) are among the most promising alternatives to conventional drugs, exhibiting broad antimicrobial spectra, rapid kinetics, and mechanisms that are difficult for bacteria to circumvent. However, the problem of discovering and engineering clinically useful AMPs with desirable properties out of large sequence spaces remains unsolved by traditional approaches. Machine learning (ML) enables fast screening of millions of compounds, generation of de novo sequences with predicted therapeutic potential, and simultaneous multiobjective optimisation of efficacy, safety, stability, and manufacturability. This review provides a critical appraisal of the current advances and prospective directions in computational discovery of AMPs that can combat resistant strains, focusing on available resources for machine learning in the domain of bioinformatics, evaluation of existing approaches to modeling peptide structure, activity, and interactions ranging from classical ML algorithms to DL and generative artificial intelligence (AI) models, and a practical roadmap of how the AMP discovery pipeline could proceed towards animal studies and clinical application through the use of active learning, fine-tuned protein language models, structural graph neural networks, and other modern techniques. Finally, we discuss challenges that may hinder a successful transition from ML-assisted design to the clinic and offer actionable recommendations to overcome them.

Indexed as

antimicrobial peptidesantimicrobial resistanceclinical trialsDLdrug discoverygeometric DLmachine learningprotein language models

Identifiers

PMID42370218
PMCPMC13310060

What Socratic holds

Textmetadata
LicenceCC BY-NC
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 Socratic graph.