Multicompartmental Lipopolyplex as Vehicle for Antigens and Genes Delivery in Vaccine Formulations

Vector design and its characterization is an area of great interest in current vaccine research. In this article, we have formulated and characterized a multicompartmental lipopolyplex, which associates multiple liposomes and polyplexes in the same complex. These particles allow the simultaneous del...

Full description

Bibliographic Details
Main Authors: Isaías Sanmartín, Luis Sendra, Inés Moret, María José Herrero, Salvador F. Aliño
Format: Article
Language:English
Published: MDPI AG 2021-02-01
Series:Pharmaceutics
Subjects:
Online Access:https://www.mdpi.com/1999-4923/13/2/281
_version_ 1797396008740585472
author Isaías Sanmartín
Luis Sendra
Inés Moret
María José Herrero
Salvador F. Aliño
author_facet Isaías Sanmartín
Luis Sendra
Inés Moret
María José Herrero
Salvador F. Aliño
author_sort Isaías Sanmartín
collection DOAJ
description Vector design and its characterization is an area of great interest in current vaccine research. In this article, we have formulated and characterized a multicompartmental lipopolyplex, which associates multiple liposomes and polyplexes in the same complex. These particles allow the simultaneous delivery of lipid or water-soluble antigens associated with genes to the same cell, in much higher amounts than conventional lipopolyplexes. The vector characterization and optimization were carried out using liposomes with entrapped carboxyfluorescein and adapted electrophoretic assays. Two types of lipopolyplexes (containing hydrophilic or lipophilic antigens) were employed to evaluate their interest in vaccination. The lipopolyplex loaded with an extract of water-soluble melanoma proteins proved to efficiently induce humoral response in murine melanoma model, increasing the levels of IgM and IgG. The specificity of the immune response induced by the lipopolyplex was demonstrated in mice with the lipopolyplex containing the GD3 ganglioside lipid antigen, abundant in melanoma cells. The levels of anti-GD3 IgG increased markedly without modifying the expression of humoral antibodies against other gangliosides.
first_indexed 2024-03-09T00:44:05Z
format Article
id doaj.art-c4d6427a3c0048b88e8b461fcb4c5709
institution Directory Open Access Journal
issn 1999-4923
language English
last_indexed 2024-03-09T00:44:05Z
publishDate 2021-02-01
publisher MDPI AG
record_format Article
series Pharmaceutics
spelling doaj.art-c4d6427a3c0048b88e8b461fcb4c57092023-12-11T17:41:01ZengMDPI AGPharmaceutics1999-49232021-02-0113228110.3390/pharmaceutics13020281Multicompartmental Lipopolyplex as Vehicle for Antigens and Genes Delivery in Vaccine FormulationsIsaías Sanmartín0Luis Sendra1Inés Moret2María José Herrero3Salvador F. Aliño4Faculty of Veterinary and Experimental Sciences, Universidad Católica de Valencia, 46001 Valencia, SpainPharmacology Department, Faculty of Medicine, Universidad de Valencia, 46010 Valencia, SpainPharmacology Department, Faculty of Medicine, Universidad de Valencia, 46010 Valencia, SpainPharmacology Department, Faculty of Medicine, Universidad de Valencia, 46010 Valencia, SpainPharmacology Department, Faculty of Medicine, Universidad de Valencia, 46010 Valencia, SpainVector design and its characterization is an area of great interest in current vaccine research. In this article, we have formulated and characterized a multicompartmental lipopolyplex, which associates multiple liposomes and polyplexes in the same complex. These particles allow the simultaneous delivery of lipid or water-soluble antigens associated with genes to the same cell, in much higher amounts than conventional lipopolyplexes. The vector characterization and optimization were carried out using liposomes with entrapped carboxyfluorescein and adapted electrophoretic assays. Two types of lipopolyplexes (containing hydrophilic or lipophilic antigens) were employed to evaluate their interest in vaccination. The lipopolyplex loaded with an extract of water-soluble melanoma proteins proved to efficiently induce humoral response in murine melanoma model, increasing the levels of IgM and IgG. The specificity of the immune response induced by the lipopolyplex was demonstrated in mice with the lipopolyplex containing the GD3 ganglioside lipid antigen, abundant in melanoma cells. The levels of anti-GD3 IgG increased markedly without modifying the expression of humoral antibodies against other gangliosides.https://www.mdpi.com/1999-4923/13/2/281lipopolyplexesmulticompartmental lipopolyplexesmelanomanon-viral gene transferantitumor immunizationvaccine
spellingShingle Isaías Sanmartín
Luis Sendra
Inés Moret
María José Herrero
Salvador F. Aliño
Multicompartmental Lipopolyplex as Vehicle for Antigens and Genes Delivery in Vaccine Formulations
Pharmaceutics
lipopolyplexes
multicompartmental lipopolyplexes
melanoma
non-viral gene transfer
antitumor immunization
vaccine
title Multicompartmental Lipopolyplex as Vehicle for Antigens and Genes Delivery in Vaccine Formulations
title_full Multicompartmental Lipopolyplex as Vehicle for Antigens and Genes Delivery in Vaccine Formulations
title_fullStr Multicompartmental Lipopolyplex as Vehicle for Antigens and Genes Delivery in Vaccine Formulations
title_full_unstemmed Multicompartmental Lipopolyplex as Vehicle for Antigens and Genes Delivery in Vaccine Formulations
title_short Multicompartmental Lipopolyplex as Vehicle for Antigens and Genes Delivery in Vaccine Formulations
title_sort multicompartmental lipopolyplex as vehicle for antigens and genes delivery in vaccine formulations
topic lipopolyplexes
multicompartmental lipopolyplexes
melanoma
non-viral gene transfer
antitumor immunization
vaccine
url https://www.mdpi.com/1999-4923/13/2/281
work_keys_str_mv AT isaiassanmartin multicompartmentallipopolyplexasvehicleforantigensandgenesdeliveryinvaccineformulations
AT luissendra multicompartmentallipopolyplexasvehicleforantigensandgenesdeliveryinvaccineformulations
AT inesmoret multicompartmentallipopolyplexasvehicleforantigensandgenesdeliveryinvaccineformulations
AT mariajoseherrero multicompartmentallipopolyplexasvehicleforantigensandgenesdeliveryinvaccineformulations
AT salvadorfalino multicompartmentallipopolyplexasvehicleforantigensandgenesdeliveryinvaccineformulations