Evidence map›Paper›PMID 30933724›Full record

ArticleMolecular therapy. Nucleic acids2019

A Facile Method for the Removal of dsRNA Contaminant from In Vitro-Transcribed mRNA.

Markus Baiersdörfer, Gábor Boros, Hiromi Muramatsu, Azita Mahiny, Irena Vlatkovic, Ugur Sahin, Katalin Karikó

Open access · goldAbstract read
In one paragraph

Article in Molecular therapy. Nucleic acids, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 360 papers.

0numbers the graph read from it
0cells of the map it votes in
360citing papers in PubMed
14.8field-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

360 citing papers in PubMed, 518 citations in OpenAlex.

  1. Article
  2. An mRNA-lipid nanoparticle vaccine targeting theMolecular therapy. Nucleic acids · 2026
    Article
  3. Article
  4. IntegratedMolecular therapy. Nucleic acids · 2026
    Article
  5. Article
  6. Article
  7. Article
  8. Review
  9. Towards mRNA therapeutics 2.0.Nature reviews. Drug discovery · 2026
    Review
  10. Article
  11. Article
  12. Cold-adapted RNA polymerase fromProceedings of the National Academy of Sciences of the United States of America · 2026
    Article
  13. Article
  14. Article
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Review

300 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 1 institution in 1 country.

Markus BaiersdörferBioNTech RNA Pharmaceuticals, 55131 Mainz, Germany. Electronic address: markus.baiersdoerfer@biontech.de.
Gábor BorosBioNTech RNA Pharmaceuticals, 55131 Mainz, Germany.
Hiromi MuramatsuBioNTech RNA Pharmaceuticals, 55131 Mainz, Germany.
Azita MahinyBioNTech RNA Pharmaceuticals, 55131 Mainz, Germany.
Irena VlatkovicBioNTech RNA Pharmaceuticals, 55131 Mainz, Germany.
Ugur SahinBioNTech RNA Pharmaceuticals, 55131 Mainz, Germany.
Katalin KarikóBioNTech RNA Pharmaceuticals, 55131 Mainz, Germany.
BioNTech (Germany) · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The increasing importance of in vitro-transcribed (IVT) mRNA for synthesizing the encoded therapeutic protein in vivo demands the manufacturing of pure mRNA products. The major contaminant in the IVT mRNA is double-stranded RNA (dsRNA), a transcriptional by-product that can be removed only by burdensome procedure requiring special instrumentation and generating hazardous waste. Here we present an alternative simple, fast, and cost-effective method involving only standard laboratory techniques. The purification of IVT mRNA is based on the selective binding of dsRNA to cellulose in an ethanol-containing buffer. We demonstrate that at least 90% of the dsRNA contaminants can be removed with a good, >65% recovery rate, regardless of the length, coding sequence, and nucleoside composition of the IVT mRNA. The procedure is scalable; purification of microgram or milligram amounts of IVT mRNA is achievable. Evaluating the impact of the mRNA purification in vivo in mice, increased translation could be measured for the administered transcripts, including the 1-methylpseudouridine-containing IVT mRNA, which no longer induced interferon (IFN)-α. The cellulose-based removal of dsRNA contaminants is an effective, reliable, and safe method to obtain highly pure IVT mRNA suitable for in vivo applications.

Indexed as

cellulose-based purificationdouble-stranded RNAin vitro transcriptionmessenger RNAnucleoside-modified RNARNA immunogenicityRNA purification

Identifiers

PMID30933724
PMCPMC6444222
OpenAlexW2915388137

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.