Evidence map›Paper›PMID 40420402›Full record

ArticleCPT: pharmacometrics & systems pharmacology2025

A Multiscale Quantitative Systems Pharmacology Model for the Development and Optimization of mRNA Vaccines.

Lorenzo Dasti, Stefano Giampiccolo, Elisa Pettinà, Giada Fiandaca, Natascia Zangani, Lorena Leonardelli, Fabio De Lima Hedayioglu, Elio Campanile, Luca Marchetti

Abstract read
In one paragraph

Article in CPT: pharmacometrics & systems pharmacology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing 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

5 citing papers in PubMed.

  1. New approach methodologies (NAMs) for preclinical and translational evaluation of mRNA-lipid nanoparticle (LNP) therapeutics.Journal of controlled release : official journal of the Controlled Release Society · 2026
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  2. Article
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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.

Lorenzo DastiDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.ORCID https://orcid.org/0009-0005-2315-4808
Stefano GiampiccoloFondazione the Microsoft Research-University of Trento Centre for Computational and Systems Biology (COSBI), Rovereto, Italy.ORCID https://orcid.org/0000-0003-4362-246X
Elisa PettinàDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.ORCID https://orcid.org/0009-0005-0530-5633
Giada FiandacaDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.ORCID https://orcid.org/0000-0002-7923-5878
Natascia ZanganiDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.ORCID https://orcid.org/0000-0003-0889-3838
Lorena LeonardelliFondazione the Microsoft Research-University of Trento Centre for Computational and Systems Biology (COSBI), Rovereto, Italy.ORCID https://orcid.org/0009-0004-0345-1250
Fabio De Lima HedayiogluSchool of Biosciences, Division of Natural Sciences, University of Kent, Canterbury, UK.ORCID https://orcid.org/0000-0003-0609-0054
Elio CampanileFondazione the Microsoft Research-University of Trento Centre for Computational and Systems Biology (COSBI), Rovereto, Italy.ORCID https://orcid.org/0009-0008-5587-7287
Luca MarchettiDepartment of Cellular, Computational and Integrative Biology (CIBIO), University of Trento, Trento, Italy.ORCID https://orcid.org/0000-0001-9043-7705

Funding

Wellcome Trust
6 · The paper itself

Abstract

The unprecedented effort to cope with the COVID-19 pandemic has unlocked the potential of mRNA vaccines as a powerful technology, set to become increasingly pervasive in the years to come. As in other areas of drug development, mathematical modeling is a pivotal tool to support and expedite the mRNA vaccine development process. This study introduces a Quantitative Systems Pharmacology (QSP) model that captures key immune responses following mRNA vaccine administration, encompassing both tissue-level and molecular-level events. The model mechanistically describes the biological processes from the uptake of mRNA by antigen-presenting cells at the injection site to the subsequent release of antibodies into the bloodstream. This two-layer model represents a first attempt to link the molecular mechanisms leading to antigen expression with the immune response, paving the way for the future integration of specific vaccine attributes, such as mRNA sequence features and nanotechnology-based delivery systems. Calibrated specifically for the BNT162b2 SARS-CoV-2 vaccine, the model has undergone successful validation across various dosing regimens and administration schedules. The results underscore the model's effectiveness in optimizing dosing strategies and highlighting critical differences in immune responses, particularly among low-responder groups such as the elderly. Furthermore, the model's adaptability has been demonstrated through its calibration for other mRNA vaccines, such as the Moderna mRNA-1273 vaccine, emphasizing its versatility and broad applicability in mRNA vaccine research and development.

Indexed as

COVID-19COVID-19 VaccinesmRNA VaccinesNetwork PharmacologyRNA, MessengerVaccine DevelopmentBNT162 VaccineHumansSARS-CoV-2Vaccines, SyntheticBNT162 VaccineCOVID-19 VaccinesmRNA VaccinesRNA, MessengerVaccines, Synthetic

Identifiers

PMID40420402
PMCPMC12256567

What OpenQuestion holds

Textmetadata
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.