Evidence map›Paper›PMID 33858437›Full record

ReviewMolecular cancer2021

mRNA therapeutics in cancer immunotherapy.

Jan D Beck, Daniel Reidenbach, Nadja Salomon, Ugur Sahin, Özlem Türeci, Mathias Vormehr, Lena M Kranz

Open access · goldAbstract readReview
In one paragraph

Review in Molecular cancer, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 222 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
222citing papers in PubMed, 1 pooled it
23.1field-weighted citation impact, top 1% of its field
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

222 citing papers in PubMed, 1 synthesis or guideline pooled it, 363 citations in OpenAlex.

  1. Pooled it
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  15. Endogenous targeting lipid nanoparticles for systemic mRNA delivery to lung cancer tumors.Journal of controlled release : official journal of the Controlled Release Society · 2026
    Article
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162 more citing papers are in PubMed but not listed here.

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

7 authors at 2 institutions in 1 country.

Jan D Beck *BioNTech SE, An der Goldgrube 12, 55131, Mainz, Germany.ORCID 0000-0002-0379-1915
Daniel Reidenbach *TRON - Translational Oncology at the University Medical Center of the Johannes Gutenberg-University gGmbH, Freiligrathstraße 12, 55131, Mainz, Germany.ORCID 0000-0002-7639-9439
Nadja Salomon *TRON - Translational Oncology at the University Medical Center of the Johannes Gutenberg-University gGmbH, Freiligrathstraße 12, 55131, Mainz, Germany.ORCID 0000-0001-8097-593X
Ugur SahinBioNTech SE, An der Goldgrube 12, 55131, Mainz, Germany.ORCID 0000-0003-0363-1564
Özlem TüreciBioNTech SE, An der Goldgrube 12, 55131, Mainz, Germany.
Mathias Vormehr *BioNTech SE, An der Goldgrube 12, 55131, Mainz, Germany.ORCID 0000-0001-7788-3380
Lena M Kranz *BioNTech SE, An der Goldgrube 12, 55131, Mainz, Germany. lena.kranz@biontech.de.ORCID 0000-0003-1943-3431
BioNTech (Germany) · DEJohannes Gutenberg University Mainz · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Synthetic mRNA provides a template for the synthesis of any given protein, protein fragment or peptide and lends itself to a broad range of pharmaceutical applications, including different modalities of cancer immunotherapy. With the ease of rapid, large scale Good Manufacturing Practice-grade mRNA production, mRNA is ideally poised not only for off-the shelf cancer vaccines but also for personalized neoantigen vaccination. The ability to stimulate pattern recognition receptors and thus an anti-viral type of innate immune response equips mRNA-based vaccines with inherent adjuvanticity. Nucleoside modification and elimination of double-stranded RNA can reduce the immunomodulatory activity of mRNA and increase and prolong protein production. In combination with nanoparticle-based formulations that increase transfection efficiency and facilitate lymphatic system targeting, nucleoside-modified mRNA enables efficient delivery of cytokines, costimulatory receptors, or therapeutic antibodies. Steady but transient production of the encoded bioactive molecule from the mRNA template can improve the pharmacokinetic, pharmacodynamic and safety properties as compared to the respective recombinant proteins. This may be harnessed for applications that benefit from a higher level of expression control, such as chimeric antigen receptor (CAR)-modified adoptive T-cell therapies. This review highlights the advancements in the field of mRNA-based cancer therapeutics, providing insights into key preclinical developments and the evolving clinical landscape.

Indexed as

Genetic TherapyImmunotherapyAnimalsAntibodiesAntigen PresentationAntigen-Presenting CellsAntigens, NeoplasmBiomarkers, TumorCancer VaccinesCytokinesDendritic CellsHumansImmunologic FactorsNeoplasmsReceptors, Antigen, T-CellRNA, MessengerAntibodiesAntigens, NeoplasmBiomarkers, TumorCancer VaccinesCytokinesImmunologic FactorsReceptors, Antigen, T-CellRNA, MessengerAntibodiesCancer immunotherapyCancer vaccinesCARsImmunomodulatory proteinsImmunoreceptorsMessenger RNA

Identifiers

PMID33858437
PMCPMC8047518
OpenAlexW3156114568

What OpenQuestion holds

Textmetadata
LicenceCC BY
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 OpenQuestion graph.