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Aripiprazole as a Candidate Treatment of COVID-19 Identified Through Genomic Analysis

Background: Antipsychotics modulate expression of inflammatory cytokines and inducible inflammatory enzymes. Elopiprazole (a phenylpiperazine antipsychotic drug in phase 1) has been characterized as a therapeutic drug to treat SARS-CoV-2 infection in a repurposing study. We aim to investigate the po...

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Autores principales: Crespo-Facorro, Benedicto, Ruiz-Veguilla, Miguel, Vázquez-Bourgon, Javier, Sánchez-Hidalgo, Ana C., Garrido-Torres, Nathalia, Cisneros, Jose M., Prieto, Carlos, Sainz, Jesus
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7982825/
https://www.ncbi.nlm.nih.gov/pubmed/33762960
http://dx.doi.org/10.3389/fphar.2021.646701
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author Crespo-Facorro, Benedicto
Ruiz-Veguilla, Miguel
Vázquez-Bourgon, Javier
Sánchez-Hidalgo, Ana C.
Garrido-Torres, Nathalia
Cisneros, Jose M.
Prieto, Carlos
Sainz, Jesus
author_facet Crespo-Facorro, Benedicto
Ruiz-Veguilla, Miguel
Vázquez-Bourgon, Javier
Sánchez-Hidalgo, Ana C.
Garrido-Torres, Nathalia
Cisneros, Jose M.
Prieto, Carlos
Sainz, Jesus
author_sort Crespo-Facorro, Benedicto
collection PubMed
description Background: Antipsychotics modulate expression of inflammatory cytokines and inducible inflammatory enzymes. Elopiprazole (a phenylpiperazine antipsychotic drug in phase 1) has been characterized as a therapeutic drug to treat SARS-CoV-2 infection in a repurposing study. We aim to investigate the potential effects of aripiprazole (an FDA approved phenylpiperazine) on COVID-19-related immunological parameters. Methods: Differential gene expression profiles of non-COVID-19 vs. COVID-19 RNA-Seq samples (CRA002390 project in GSA database) and drug-naïve patients with non-affective psychosis at baseline and after three months of aripiprazole treatment were identified. An integrative transcriptomic analyses of aripiprazole effects on differentially expressed genes in COVID-19 patients was performed. Findings: 82 out the 377 genes (21.7%) with expression significantly altered by aripiprazole have also their expression altered in COVID-19 patients and in 93.9% of these genes their expression is reverted by aripiprazole. The number of common genes with expression altered in both analyses is significantly higher than expected (Fisher’s Exact Test, two tail; p value = 3.2e-11). 11 KEGG pathways were significantly enriched with genes with altered expression both in COVID-19 patients and aripiprazole medicated non-affective psychosis patients (p adj<0.05). The most significant pathways were associated to immune responses and mechanisms of hyperinflammation-driven pathology (i.e.,“inflammatory bowel disease (IBD)” (the most significant pathway with a p adj of 0.00021), “Th1 and Th2 cell differentiation” and “B cell receptor signaling pathway”) that have been also associated with COVID19 clinical outcome. Interpretation: This exploratory investigation may provide further support to the notion that a protective effect is exerted by aripiprazole (phenylpiperazine) by modulating the expression of genes that have shown to be altered in COVID-19 patients. Along with many ongoing studies and clinical trials, repurposing available medications could be of use in countering SARS-CoV-2 infection, but require further studies and trials.
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spelling pubmed-79828252021-03-23 Aripiprazole as a Candidate Treatment of COVID-19 Identified Through Genomic Analysis Crespo-Facorro, Benedicto Ruiz-Veguilla, Miguel Vázquez-Bourgon, Javier Sánchez-Hidalgo, Ana C. Garrido-Torres, Nathalia Cisneros, Jose M. Prieto, Carlos Sainz, Jesus Front Pharmacol Pharmacology Background: Antipsychotics modulate expression of inflammatory cytokines and inducible inflammatory enzymes. Elopiprazole (a phenylpiperazine antipsychotic drug in phase 1) has been characterized as a therapeutic drug to treat SARS-CoV-2 infection in a repurposing study. We aim to investigate the potential effects of aripiprazole (an FDA approved phenylpiperazine) on COVID-19-related immunological parameters. Methods: Differential gene expression profiles of non-COVID-19 vs. COVID-19 RNA-Seq samples (CRA002390 project in GSA database) and drug-naïve patients with non-affective psychosis at baseline and after three months of aripiprazole treatment were identified. An integrative transcriptomic analyses of aripiprazole effects on differentially expressed genes in COVID-19 patients was performed. Findings: 82 out the 377 genes (21.7%) with expression significantly altered by aripiprazole have also their expression altered in COVID-19 patients and in 93.9% of these genes their expression is reverted by aripiprazole. The number of common genes with expression altered in both analyses is significantly higher than expected (Fisher’s Exact Test, two tail; p value = 3.2e-11). 11 KEGG pathways were significantly enriched with genes with altered expression both in COVID-19 patients and aripiprazole medicated non-affective psychosis patients (p adj<0.05). The most significant pathways were associated to immune responses and mechanisms of hyperinflammation-driven pathology (i.e.,“inflammatory bowel disease (IBD)” (the most significant pathway with a p adj of 0.00021), “Th1 and Th2 cell differentiation” and “B cell receptor signaling pathway”) that have been also associated with COVID19 clinical outcome. Interpretation: This exploratory investigation may provide further support to the notion that a protective effect is exerted by aripiprazole (phenylpiperazine) by modulating the expression of genes that have shown to be altered in COVID-19 patients. Along with many ongoing studies and clinical trials, repurposing available medications could be of use in countering SARS-CoV-2 infection, but require further studies and trials. Frontiers Media S.A. 2021-03-02 /pmc/articles/PMC7982825/ /pubmed/33762960 http://dx.doi.org/10.3389/fphar.2021.646701 Text en Copyright © 2021 Crespo-Facorro, Ruiz-Veguilla, Vázquez-Bourgon, Sánchez-Hidalgo, Garrido-Torres, Cisneros, Prieto and Sainz. http://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
Crespo-Facorro, Benedicto
Ruiz-Veguilla, Miguel
Vázquez-Bourgon, Javier
Sánchez-Hidalgo, Ana C.
Garrido-Torres, Nathalia
Cisneros, Jose M.
Prieto, Carlos
Sainz, Jesus
Aripiprazole as a Candidate Treatment of COVID-19 Identified Through Genomic Analysis
title Aripiprazole as a Candidate Treatment of COVID-19 Identified Through Genomic Analysis
title_full Aripiprazole as a Candidate Treatment of COVID-19 Identified Through Genomic Analysis
title_fullStr Aripiprazole as a Candidate Treatment of COVID-19 Identified Through Genomic Analysis
title_full_unstemmed Aripiprazole as a Candidate Treatment of COVID-19 Identified Through Genomic Analysis
title_short Aripiprazole as a Candidate Treatment of COVID-19 Identified Through Genomic Analysis
title_sort aripiprazole as a candidate treatment of covid-19 identified through genomic analysis
topic Pharmacology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7982825/
https://www.ncbi.nlm.nih.gov/pubmed/33762960
http://dx.doi.org/10.3389/fphar.2021.646701
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