Evidence map›Paper›PMID 40789921›Full record

ArticleNature nanotechnology2025

Compact polyethylenimine-complexed mRNA vaccines.

Jorge Moreno Herrero, Theo B Stahl, Stephanie Erbar, Konrad Maxeiner, Anne Schlegel, Tijana Bacic, Jens Schumacher, Leide P Cavalcanti, Martin A Schroer, Dmitri I Svergun and 2 more

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Article in Nature nanotechnology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

  1. Article
  2. Review
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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

12 authors.

Jorge Moreno HerreroBioNTech SE, Mainz, Germany.
Theo B StahlBioNTech SE, Mainz, Germany.
Stephanie ErbarBioNTech SE, Mainz, Germany.ORCID http://orcid.org/0000-0003-1898-4776
Konrad MaxeinerBioNTech SE, Mainz, Germany.
Anne SchlegelBioNTech SE, Mainz, Germany.
Tijana BacicBioNTech SE, Mainz, Germany.
Jens SchumacherBioNTech SE, Mainz, Germany.
Leide P CavalcantiISIS Pulsed Neutron and Muon Source, Harwell, UK.ORCID http://orcid.org/0000-0002-0408-0058
Martin A SchroerEuropean Molecular Biology Laboratory, Hamburg Outstation, Hamburg, Germany.ORCID http://orcid.org/0000-0002-0747-3965
Dmitri I SvergunEuropean Molecular Biology Laboratory, Hamburg Outstation, Hamburg, Germany.
Ugur SahinBioNTech SE, Mainz, Germany. ugur.sahin@biontech.de.ORCID http://orcid.org/0000-0003-0363-1564
Heinrich HaasBioNTech SE, Mainz, Germany. haashein@uni-mainz.de.ORCID http://orcid.org/0000-0002-5517-5970

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Here we describe formulations comprising individual, polymer-complexed self-amplifying RNA (saRNA) molecules, designed for vaccination against infectious diseases and other prophylactic and therapeutic applications. When exposed to a large excess of the cationic polymer polyethylenimine (PEI), the single saRNA molecules in solution reorganize from an extended to a globular organization, characterized by a high packing density, low polymer mass fraction and, consequently, a very small size of the polyplex nanoparticles of about 30 nm. This format of PEI-complexed saRNA exhibits enhanced biological activity in comparison with previously described saRNA/PEI formulations, both in vitro and in vivo. In vaccination models, relevant immune responses at lower doses are achieved, offering potential advantages for practical use. We found that the single PEI-complexed RNA molecules are also present in conventional formulations to some degree. The direct correlation between the single-molecule fraction with activity suggests that it is this format that predominantly contributes to activity in the different formulation types. Complexation is driven by mechanisms of self-assembly between oppositely charged polyelectrolytes, making this protocol broadly applicable to various cationic polymers and RNA constructs. With their small size and good stability in biofluids, these compacted RNA molecules are also promising for the systemic delivery of genetic material to compartments that are difficult to reach with larger particles.

Indexed as

mRNA VaccinesPolyethyleneimineRNA, MessengerAnimalsHumansMiceNanoparticlesmRNA VaccinesPolyethyleneimineRNA, Messenger

Identifiers

What Socratic holds

Textmetadata
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 Socratic graph.