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Psychotropic drugs interaction with the lipid nanoparticle of COVID-19 mRNA therapeutics

The messenger RNA (mRNA) vaccines for COVID-19, Pfizer-BioNTech and Moderna, were authorized in the US on an emergency basis in December of 2020. The rapid distribution of these therapeutics around the country and the world led to millions of people being vaccinated in a short time span, an action t...

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Autores principales: Sfera, Adonis, Hazan, Sabine, Anton, Jonathan J., Sfera, Dan O., Andronescu, Christina V., Sasannia, Sarvin, Rahman, Leah, Kozlakidis, Zisis
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503827/
https://www.ncbi.nlm.nih.gov/pubmed/36160443
http://dx.doi.org/10.3389/fphar.2022.995481
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author Sfera, Adonis
Hazan, Sabine
Anton, Jonathan J.
Sfera, Dan O.
Andronescu, Christina V.
Sasannia, Sarvin
Rahman, Leah
Kozlakidis, Zisis
author_facet Sfera, Adonis
Hazan, Sabine
Anton, Jonathan J.
Sfera, Dan O.
Andronescu, Christina V.
Sasannia, Sarvin
Rahman, Leah
Kozlakidis, Zisis
author_sort Sfera, Adonis
collection PubMed
description The messenger RNA (mRNA) vaccines for COVID-19, Pfizer-BioNTech and Moderna, were authorized in the US on an emergency basis in December of 2020. The rapid distribution of these therapeutics around the country and the world led to millions of people being vaccinated in a short time span, an action that decreased hospitalization and death but also heightened the concerns about adverse effects and drug-vaccine interactions. The COVID-19 mRNA vaccines are of particular interest as they form the vanguard of a range of other mRNA therapeutics that are currently in the development pipeline, focusing both on infectious diseases as well as oncological applications. The Vaccine Adverse Event Reporting System (VAERS) has gained additional attention during the COVID-19 pandemic, specifically regarding the rollout of mRNA therapeutics. However, for VAERS, absence of a reporting platform for drug-vaccine interactions left these events poorly defined. For example, chemotherapy, anticonvulsants, and antimalarials were documented to interfere with the mRNA vaccines, but much less is known about the other drugs that could interact with these therapeutics, causing adverse events or decreased efficacy. In addition, SARS-CoV-2 exploitation of host cytochrome P450 enzymes, reported in COVID-19 critical illness, highlights viral interference with drug metabolism. For example, patients with severe psychiatric illness (SPI) in treatment with clozapine often displayed elevated drug levels, emphasizing drug-vaccine interaction.
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spelling pubmed-95038272022-09-24 Psychotropic drugs interaction with the lipid nanoparticle of COVID-19 mRNA therapeutics Sfera, Adonis Hazan, Sabine Anton, Jonathan J. Sfera, Dan O. Andronescu, Christina V. Sasannia, Sarvin Rahman, Leah Kozlakidis, Zisis Front Pharmacol Pharmacology The messenger RNA (mRNA) vaccines for COVID-19, Pfizer-BioNTech and Moderna, were authorized in the US on an emergency basis in December of 2020. The rapid distribution of these therapeutics around the country and the world led to millions of people being vaccinated in a short time span, an action that decreased hospitalization and death but also heightened the concerns about adverse effects and drug-vaccine interactions. The COVID-19 mRNA vaccines are of particular interest as they form the vanguard of a range of other mRNA therapeutics that are currently in the development pipeline, focusing both on infectious diseases as well as oncological applications. The Vaccine Adverse Event Reporting System (VAERS) has gained additional attention during the COVID-19 pandemic, specifically regarding the rollout of mRNA therapeutics. However, for VAERS, absence of a reporting platform for drug-vaccine interactions left these events poorly defined. For example, chemotherapy, anticonvulsants, and antimalarials were documented to interfere with the mRNA vaccines, but much less is known about the other drugs that could interact with these therapeutics, causing adverse events or decreased efficacy. In addition, SARS-CoV-2 exploitation of host cytochrome P450 enzymes, reported in COVID-19 critical illness, highlights viral interference with drug metabolism. For example, patients with severe psychiatric illness (SPI) in treatment with clozapine often displayed elevated drug levels, emphasizing drug-vaccine interaction. Frontiers Media S.A. 2022-09-09 /pmc/articles/PMC9503827/ /pubmed/36160443 http://dx.doi.org/10.3389/fphar.2022.995481 Text en Copyright © 2022 Sfera, Hazan, Anton, Sfera, Andronescu, Sasannia, Rahman and Kozlakidis. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pharmacology
Sfera, Adonis
Hazan, Sabine
Anton, Jonathan J.
Sfera, Dan O.
Andronescu, Christina V.
Sasannia, Sarvin
Rahman, Leah
Kozlakidis, Zisis
Psychotropic drugs interaction with the lipid nanoparticle of COVID-19 mRNA therapeutics
title Psychotropic drugs interaction with the lipid nanoparticle of COVID-19 mRNA therapeutics
title_full Psychotropic drugs interaction with the lipid nanoparticle of COVID-19 mRNA therapeutics
title_fullStr Psychotropic drugs interaction with the lipid nanoparticle of COVID-19 mRNA therapeutics
title_full_unstemmed Psychotropic drugs interaction with the lipid nanoparticle of COVID-19 mRNA therapeutics
title_short Psychotropic drugs interaction with the lipid nanoparticle of COVID-19 mRNA therapeutics
title_sort psychotropic drugs interaction with the lipid nanoparticle of covid-19 mrna therapeutics
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9503827/
https://www.ncbi.nlm.nih.gov/pubmed/36160443
http://dx.doi.org/10.3389/fphar.2022.995481
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