Cargando…

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

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 n...

Descripción completa

Detalles Bibliográficos
Autores principales: Ndeupen, Sonia, Qin, Zhen, Jacobsen, Sonya, Estanbouli, Henri, Bouteau, Aurélie, Igyártó, Botond Z.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Cold Spring Harbor Laboratory 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941620/
https://www.ncbi.nlm.nih.gov/pubmed/33688649
http://dx.doi.org/10.1101/2021.03.04.430128
_version_ 1783662164427407360
author Ndeupen, Sonia
Qin, Zhen
Jacobsen, Sonya
Estanbouli, Henri
Bouteau, Aurélie
Igyártó, Botond Z.
author_facet Ndeupen, Sonia
Qin, Zhen
Jacobsen, Sonya
Estanbouli, Henri
Bouteau, Aurélie
Igyártó, Botond Z.
author_sort Ndeupen, Sonia
collection PubMed
description 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.
format Online
Article
Text
id pubmed-7941620
institution National Center for Biotechnology Information
language English
publishDate 2021
publisher Cold Spring Harbor Laboratory
record_format MEDLINE/PubMed
spelling pubmed-79416202021-03-10 The mRNA-LNP platform’s lipid nanoparticle component used in preclinical vaccine studies is highly inflammatory Ndeupen, Sonia Qin, Zhen Jacobsen, Sonya Estanbouli, Henri Bouteau, Aurélie Igyártó, Botond Z. bioRxiv Article 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. Cold Spring Harbor Laboratory 2021-07-23 /pmc/articles/PMC7941620/ /pubmed/33688649 http://dx.doi.org/10.1101/2021.03.04.430128 Text en https://creativecommons.org/licenses/by-nc-nd/4.0/This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License (https://creativecommons.org/licenses/by-nc-nd/4.0/) , which allows reusers to copy and distribute the material in any medium or format in unadapted form only, for noncommercial purposes only, and only so long as attribution is given to the creator.
spellingShingle Article
Ndeupen, Sonia
Qin, Zhen
Jacobsen, Sonya
Estanbouli, Henri
Bouteau, Aurélie
Igyártó, Botond Z.
The mRNA-LNP platform’s lipid nanoparticle component used in preclinical vaccine studies is highly inflammatory
title The mRNA-LNP platform’s lipid nanoparticle component used in preclinical vaccine studies is highly inflammatory
title_full The mRNA-LNP platform’s lipid nanoparticle component used in preclinical vaccine studies is highly inflammatory
title_fullStr The mRNA-LNP platform’s lipid nanoparticle component used in preclinical vaccine studies is highly inflammatory
title_full_unstemmed The mRNA-LNP platform’s lipid nanoparticle component used in preclinical vaccine studies is highly inflammatory
title_short The mRNA-LNP platform’s lipid nanoparticle component used in preclinical vaccine studies is highly inflammatory
title_sort mrna-lnp platform’s lipid nanoparticle component used in preclinical vaccine studies is highly inflammatory
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7941620/
https://www.ncbi.nlm.nih.gov/pubmed/33688649
http://dx.doi.org/10.1101/2021.03.04.430128
work_keys_str_mv AT ndeupensonia themrnalnpplatformslipidnanoparticlecomponentusedinpreclinicalvaccinestudiesishighlyinflammatory
AT qinzhen themrnalnpplatformslipidnanoparticlecomponentusedinpreclinicalvaccinestudiesishighlyinflammatory
AT jacobsensonya themrnalnpplatformslipidnanoparticlecomponentusedinpreclinicalvaccinestudiesishighlyinflammatory
AT estanboulihenri themrnalnpplatformslipidnanoparticlecomponentusedinpreclinicalvaccinestudiesishighlyinflammatory
AT bouteauaurelie themrnalnpplatformslipidnanoparticlecomponentusedinpreclinicalvaccinestudiesishighlyinflammatory
AT igyartobotondz themrnalnpplatformslipidnanoparticlecomponentusedinpreclinicalvaccinestudiesishighlyinflammatory
AT ndeupensonia mrnalnpplatformslipidnanoparticlecomponentusedinpreclinicalvaccinestudiesishighlyinflammatory
AT qinzhen mrnalnpplatformslipidnanoparticlecomponentusedinpreclinicalvaccinestudiesishighlyinflammatory
AT jacobsensonya mrnalnpplatformslipidnanoparticlecomponentusedinpreclinicalvaccinestudiesishighlyinflammatory
AT estanboulihenri mrnalnpplatformslipidnanoparticlecomponentusedinpreclinicalvaccinestudiesishighlyinflammatory
AT bouteauaurelie mrnalnpplatformslipidnanoparticlecomponentusedinpreclinicalvaccinestudiesishighlyinflammatory
AT igyartobotondz mrnalnpplatformslipidnanoparticlecomponentusedinpreclinicalvaccinestudiesishighlyinflammatory