Evidence map›Paper›PMID 40133349›Full record

ArticleScientific reports2025

A novel in-vitro expression assay by LC/MS/MS enables multi-antigen mRNA vaccine characterization.

Hanliu Leah Wang, Kimia Kajbaf, Brian C Gau, Andrew W Dawdy, Rachel Edwards, Bradley Bare, Gianna Raymundo, Jose Iturrizaga, Chase Ernsky, Michael Walker and 9 more

Abstract read
In one paragraph

Article in Scientific reports, 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. Article
  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

19 authors.

Hanliu Leah WangBioTherapeutics Pharmaceutical Sciences, Pfizer Inc, Chesterfield, MO, USA.
Kimia KajbafBioTherapeutics Pharmaceutical Sciences, Pfizer Inc, Chesterfield, MO, USA.
Brian C GauBioTherapeutics Pharmaceutical Sciences, Pfizer Inc, Chesterfield, MO, USA.
Andrew W DawdyBioTherapeutics Pharmaceutical Sciences, Pfizer Inc, Chesterfield, MO, USA.
Rachel EdwardsBioTherapeutics Pharmaceutical Sciences, Pfizer Inc, Chesterfield, MO, USA.
Bradley BareBioTherapeutics Pharmaceutical Sciences, Pfizer Inc, Chesterfield, MO, USA.
Gianna RaymundoBioTherapeutics Pharmaceutical Sciences, Pfizer Inc, Chesterfield, MO, USA.
Jose IturrizagaBioTherapeutics Pharmaceutical Sciences, Pfizer Inc, Chesterfield, MO, USA.
Chase ErnskyBioTherapeutics Pharmaceutical Sciences, Pfizer Inc, Chesterfield, MO, USA.
Michael WalkerBioTherapeutics Pharmaceutical Sciences, Pfizer Inc, Chesterfield, MO, USA.
Emilia B ByrneBioTherapeutics Pharmaceutical Sciences, Pfizer Inc, Chesterfield, MO, USA.
James BoslettVaccine Research and Development, Pfizer Inc, Pearl River, NY, USA.
Adam CampbellVaccine Research and Development, Pfizer Inc, Pearl River, NY, USA.
Roman MatthessenDrug Product Center of Excellence, Pfizer Manufacturing Belgium, Puurs‑Sint‑Amands, Belgium.
Ben GoffinDrug Product Center of Excellence, Pfizer Manufacturing Belgium, Puurs‑Sint‑Amands, Belgium.
David CirelliBioTherapeutics Pharmaceutical Sciences, Pfizer Inc, Andover, MA, USA.
Jason C RouseBioTherapeutics Pharmaceutical Sciences, Pfizer Inc, Andover, MA, USA.
Robbe Van PottelbergeDrug Product Center of Excellence, Pfizer Manufacturing Belgium, Puurs‑Sint‑Amands, Belgium. robbe.vanpottelberge@pfizer.com.
Olga V FrieseBioTherapeutics Pharmaceutical Sciences, Pfizer Inc, Chesterfield, MO, USA. olga.v.friese@pfizer.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The new era of messenger RNA (mRNA) vaccines has led to development of a novel, state-of-the-art characterization method for this class of molecules. Currently, flow cytometry-based assays with antigen-specific antibodies are utilized for monitoring in-vitro expression (IVE) of mRNA. Here we present development, optimization, and application of an in-vitro expression liquid chromatography tandem mass spectrometry (IVE-LC/MS/MS) assay as an orthogonal method to IVE-flow cytometry that can be used for in-depth characterization of the expressed protein antigens and monitoring their relative expression levels in the cell post-mRNA transfection. The IVE-LC/MS/MS assessment accomplished the detection of influenza hemagglutinin (HA) antigens of four distinct strains simultaneously. The workflow is presented here, highlighting the optimization of all necessary steps required for protein purification and mass spectrometry method setup. The IVE-LC/MS/MS assay is a robust and versatile technique that complements the IVE-flow cytometry method and offers several advantages, such as being antibody-free, capable of multiplexing, and highly sensitive and selective. The various studies in this work, including evaluating dose-response relationships, refining transfection protocols, and examining mRNA-LNP stability under various conditions showcase the significant benefits of applying IVE-LC/MS/MS across different experimental settings. IVE-LC/MS/MS is a powerful tool for understanding and improving the performance and quality of mRNA LNPs.

Indexed as

Antigens, ViralInfluenza VaccinesmRNA VaccinesRNA, MessengerTandem Mass SpectrometryAnimalsChromatography, LiquidFlow CytometryHemagglutinin Glycoproteins, Influenza VirusHumansAntigens, ViralHemagglutinin Glycoproteins, Influenza VirusInfluenza VaccinesmRNA VaccinesRNA, Messenger

Identifiers

PMID40133349
PMCPMC11937333

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Registered trials

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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.