Evidence map›Paper›PMID 41106780›Full record

ReviewVirus research2025

Next-generation antiviral peptides: AI-driven design, translational delivery platforms, and future therapeutic directions.

Maryam Mashhadi Abolghasem Shirazi, Setareh Haghighat, Zahra Nikbakht, Elaheh Salimkia, Armity Kiumarsy

Abstract readReview
In one paragraph

Review in Virus research, 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. Review
  2. 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

5 authors.

Maryam Mashhadi Abolghasem ShiraziDepartment of Microbiology, TeMS.C., Islamic Azad University, Tehran, Iran.
Setareh HaghighatDepartment of Microbiology, TeMS.C., Islamic Azad University, Tehran, Iran. Electronic address: haghighat.s@iau.ac.ir.
Zahra NikbakhtDepartment of Microbiology, TeMS.C., Islamic Azad University, Tehran, Iran.
Elaheh SalimkiaDepartment of Microbiology, TeMS.C., Islamic Azad University, Tehran, Iran.
Armity KiumarsyDepartment of Microbiology, TeMS.C., Islamic Azad University, Tehran, Iran.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Antiviral peptides (AVPs) are emerging as next-generation therapeutics due to their broad-spectrum activity, low toxicity, and ability to overcome drug resistance. The objective of this review is to provide an integrated perspective on AVP research, with particular emphasis on artificial intelligence (AI)-driven discovery, novel delivery strategies, and translational applications. We first summarize the origins, mechanisms, and structural diversity of AVPs. We then highlight recent advances in computational pipelines, including machine learning, deep learning, generative adversarial networks (GANs), large language models (LLMs), and reinforcement learning frameworks for de novo peptide design. Translational aspects are addressed by discussing novel delivery systems such as nanoparticles, hydrogels, and intranasal/inhalable formulations, as well as clinical trial examples (like, enfuvirtide (T-20), sifuvirtide, lactoferrin-based formulations, PAC-113). Finally, we explore future directions, including CRISPR- and mRNA-based peptide delivery and synergies with immune checkpoint inhibitors. By combining classical mechanisms with AI-driven design and innovative delivery platforms, this review underscores the potential of AVPs as versatile antiviral agents ready for clinical translation.

Indexed as

Antiviral AgentsArtificial IntelligenceDrug Delivery SystemsDrug DesignPeptidesAnimalsHumansAntiviral AgentsPeptidesAntiviral peptidesArtificial intelligenceDrug resistanceGenerative adversarial networksLarge language modelsMachine learning

Identifiers

PMID41106780
PMCPMC12713194

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.