Evidence map›Paper›PMID 33688649›Full record

ArticlebioRxiv : the preprint server for biology2021

The mRNA-LNP platform's lipid nanoparticle component used in preclinical vaccine studies is highly inflammatory.

Sonia Ndeupen, Zhen Qin, Sonya Jacobsen, Henri Estanbouli, Aurélie Bouteau, Botond Z Igyártó

Open access · greenAbstract readPreprint
In one paragraph

Article in bioRxiv : the preprint server for biology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed, 56 citations in OpenAlex.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors at 1 institution in 1 country.

Sonia NdeupenThomas Jefferson University, Department of Microbiology and Immunology, Philadelphia, PA.
Zhen QinThomas Jefferson University, Department of Microbiology and Immunology, Philadelphia, PA.
Sonya JacobsenThomas Jefferson University, Department of Microbiology and Immunology, Philadelphia, PA.
Henri EstanbouliThomas Jefferson University, Department of Microbiology and Immunology, Philadelphia, PA.
Aurélie BouteauThomas Jefferson University, Department of Microbiology and Immunology, Philadelphia, PA.
Botond Z IgyártóThomas Jefferson University, Department of Microbiology and Immunology, Philadelphia, PA.
Thomas Jefferson University · US

Funding

DC-subset-tailored vaccinesR01AI146420 · NIAID · THOMAS JEFFERSON UNIVERSITY · PI IGYARTO, BOTOND Z · 2020 to 2024
$1.9M
NIAID NIH HHS R01 AI146420
6 · The paper itself

Abstract

Vaccines based on mRNA-containing lipid nanoparticles (LNPs) are a promising new platform used by two leading vaccines against coronavirus disease in 2019 (COVID-19). Clinical trials and ongoing vaccinations present with very high protection levels and varying degrees of side effects. However, the nature of the reported side effects remains poorly defined. Here we present evidence that LNPs used in many preclinical studies are highly inflammatory in mice. Intradermal injection of these LNPs led to rapid and robust inflammatory responses, characterized by massive neutrophil infiltration, activation of diverse inflammatory pathways, and production of various inflammatory cytokines and chemokines. The same dose of LNP delivered intranasally led to similar inflammatory responses in the lung and resulted in a high mortality rate. In summary, here we show that the LNPs used for many preclinical studies are highly inflammatory. Thus, their potent adjuvant activity and reported superiority comparing to other adjuvants in supporting the induction of adaptive immune responses likely stem from their inflammatory nature. Furthermore, the preclinical LNPs are similar to the ones used for human vaccines, which could also explain the observed side effects in humans using this platform.

Indexed as

inflammationLNPmRNA-LNP vaccineSARS-CoV-2 vaccineside-effects

Identifiers

PMID33688649
PMCPMC7941620
OpenAlexW3135103990

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.