Long-Term Liver Expression of an Apolipoprotein A-I Mimetic Peptide Attenuates Interferon-Alpha-Induced Inflammation and Promotes Antiviral Activity.
Animals
Antiviral Agents
/ pharmacology
Apolipoprotein A-I
/ agonists
Dependovirus
/ genetics
Female
Gene Expression Regulation, Viral
Gene Silencing
Genetic Vectors
/ genetics
Inflammation
/ etiology
Interferon-alpha
/ biosynthesis
Lipoproteins
/ blood
Liver
/ metabolism
Liver X Receptors
/ metabolism
Mice
Mice, Inbred C57BL
PPAR alpha
/ metabolism
PPAR gamma
/ metabolism
Pancytopenia
/ etiology
Proteome
RNA, Messenger
/ biosynthesis
Recombinant Proteins
/ biosynthesis
Retinoid X Receptors
/ metabolism
Specific Pathogen-Free Organisms
Transgenes
adeno-associated virus
antiviral
apolipoprotein A-I mimetic peptide
liver
type I Interferon
Journal
Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960
Informations de publication
Date de publication:
2020
2020
Historique:
received:
22
10
2020
accepted:
29
12
2020
entrez:
12
3
2021
pubmed:
13
3
2021
medline:
8
7
2021
Statut:
epublish
Résumé
Apolipoprotein A-I mimetic peptides are amphipathic alpha-helix peptides that display similar functions to apolipoprotein A-I. Preclinical and clinical studies have demonstrated the safety and efficacy of apolipoprotein A-I mimetic peptides in multiple indications associated with inflammatory processes. In this study, we evaluated the effect of the long-term expression of L37pA in the liver by an adeno-associated virus (AAV-L37pA) on the expression of an adeno-associated virus encoding interferon-alpha (AAV-IFNα). Long-term IFNα expression in the liver leads to lethal hematological toxicity one month after AAV administration. Concomitant administration of AAV-L37pA prevented the lethal toxicity since the IFNα expression was reduced one month after AAV administration. To identify the mechanism of action of L37pA, a genomic and proteomic analysis was performed 15 days after AAV administration when a similar level of IFNα and interferon-stimulated genes were observed in mice treated with AAV-IFNα alone and in mice treated with AAV-IFNα and AAV-L37pA. The coexpression of the apolipoprotein A-I mimetic peptide L37pA with IFNα modulated the gene expression program of IFNα, inducing a significant reduction in inflammatory pathways affecting pathogen-associated molecular patterns receptor, dendritic cells, NK cells and Th1 immune response. The proteomic analysis confirmed the impact of the L37pA activity on several inflammatory pathways and indicated an activation of LXR/RXR and PPPARα/γ nuclear receptors. Thus, long-term expression of L37pA induces an anti-inflammatory effect in the liver that allows silencing of IFNα expression mediated by an adeno-associated virus.
Identifiants
pubmed: 33708194
doi: 10.3389/fimmu.2020.620283
pmc: PMC7940203
doi:
Substances chimiques
Antiviral Agents
0
Apoa1 protein, mouse
0
Apolipoprotein A-I
0
Ifna1 protein, mouse
0
Interferon-alpha
0
Lipoproteins
0
Liver X Receptors
0
Nr1h3 protein, mouse
0
PPAR alpha
0
PPAR gamma
0
Pparg protein, mouse
0
Proteome
0
RNA, Messenger
0
Recombinant Proteins
0
Retinoid X Receptors
0
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
620283Informations de copyright
Copyright © 2021 Fernandez-Sendin, Di Trani, Bella, Vasquez, Ardaiz, Gomar, Arrizabalaga, Ciordia, Corrales, Aranda and Berraondo.
Déclaration de conflit d'intérêts
The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
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