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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...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Cold Spring Harbor Laboratory
2021
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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 |
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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 |
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