Evidence map›Paper›PMID 42090365›Full record

ArticlePloS one2026

Design and in silico evaluation of an mRNA vaccine against HTLV-1 using AI-driven reverse vaccinology approaches.

Nadia Seifi, Navid Nezafat, Mohammad Soroosh Hajizade, Manica Negahdaripour

Abstract read
In one paragraph

Article in PloS one, 2026. 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
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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

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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

4 authors.

Nadia SeifiDepartment of Pharmaceutical Biotechnology, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID https://orcid.org/0009-0009-1333-6738
Navid NezafatPharmaceutical Sciences Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
Mohammad Soroosh HajizadeDepartment of Pharmaceutical Biotechnology, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.
Manica NegahdaripourDepartment of Pharmaceutical Biotechnology, School of Pharmacy, Shiraz University of Medical Sciences, Shiraz, Iran.ORCID https://orcid.org/0000-0002-4265-1499

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Human T-lymphotropic virus type 1 (HTLV-1) is the first discovered human oncogenic retrovirus that can cause adult T-cell leukemia/lymphoma, HTLV-1-associated myelopathy/tropical spastic paraparesis, and several other diseases. Due to the poor prognosis of these diseases and the limited therapeutic modalities, the need for an HTLV-1 vaccine is crucial. The current study has used an artificial intelligence-driven reverse vaccinology approach to design an mRNA vaccine against HTLV-1. The two most antigenic proteins of the virus were selected and analyzed using multiple immunoinformatics tools to identify the antigenic immunodominant epitopes for T- and B-cells. Subsequently, the final selected epitopes and the adjuvant were connected using proper linkers. Subsequently, multiple 3D structures were modeled for the vaccine. After refining and evaluating the modeled structures, the best model was selected as the final candidate vaccine structure. The proposed mRNA structure is a potential vaccine with suitable immunological and physicochemical properties against HTLV-1. Docking and simulation analyses showed a proper interaction between the vaccine and the corresponding receptor of the employed adjuvant. However, additional experimental studies are required to further confirm the vaccine's efficacy.

Indexed as

Artificial IntelligenceHTLV-I InfectionsHuman T-lymphotropic virus 1mRNA VaccinesReverse VaccinologyRNA, MessengerViral VaccinesComputer SimulationHumansImmunoinformaticsMolecular Docking SimulationmRNA VaccinesRNA, MessengerViral Vaccines

Identifiers

PMID42090365
PMCPMC13148667

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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.