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Ultradeformable Archaeosomes for Needle Free Nanovaccination with Leishmania braziliensis Antigens

Total antigens from Leishmania braziliensis promastigotes, solubilized with sodium cholate (dsLp), were formulated within ultradeformable nanovesicles (dsLp-ultradeformable archaeosomes, (dsLp-UDA), and dsLp-ultradeformable liposomes (dsLp-UDL)) and topically administered to Balb/c mice. Ultradeform...

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Autores principales: Higa, Leticia H., Arnal, Laura, Vermeulen, Mónica, Perez, Ana Paula, Schilrreff, Priscila, Mundiña-Weilenmann, Cecilia, Yantorno, Osvaldo, Vela, María Elena, Morilla, María José, Romero, Eder Lilia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4774928/
https://www.ncbi.nlm.nih.gov/pubmed/26934726
http://dx.doi.org/10.1371/journal.pone.0150185
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author Higa, Leticia H.
Arnal, Laura
Vermeulen, Mónica
Perez, Ana Paula
Schilrreff, Priscila
Mundiña-Weilenmann, Cecilia
Yantorno, Osvaldo
Vela, María Elena
Morilla, María José
Romero, Eder Lilia
author_facet Higa, Leticia H.
Arnal, Laura
Vermeulen, Mónica
Perez, Ana Paula
Schilrreff, Priscila
Mundiña-Weilenmann, Cecilia
Yantorno, Osvaldo
Vela, María Elena
Morilla, María José
Romero, Eder Lilia
author_sort Higa, Leticia H.
collection PubMed
description Total antigens from Leishmania braziliensis promastigotes, solubilized with sodium cholate (dsLp), were formulated within ultradeformable nanovesicles (dsLp-ultradeformable archaeosomes, (dsLp-UDA), and dsLp-ultradeformable liposomes (dsLp-UDL)) and topically administered to Balb/c mice. Ultradeformable nanovesicles can penetrate the intact stratum corneum up to the viable epidermis, with no aid of classical permeation enhancers that can damage the barrier function of the skin. Briefly, 100 nm unilamellar dsLp-UDA (soybean phosphatidylcholine: Halorubrum tebenquichense total polar lipids (TPL): sodium cholate, 3:3:1 w:w) of -31.45 mV Z potential, containing 4.84 ± 0.53% w/w protein/lipid dsLp, 235 KPa Young modulus were prepared. In vitro, dsLp-UDA was extensively taken up by J774A1 and bone marrow derive cells, and the only that induced an immediate secretion of IL-6, IL-12p40 and TNF-α, followed by IL-1β, by J774A1 cells. Such extensive uptake is a key feature of UDA ascribed to the highly negatively charged archaeolipids of the TPL, which are recognized by a receptor specialized in uptake and not involved in downstream signaling. Despite dsLp alone was also immunostimulatory on J774A1 cells, applied twice a week on consecutive days along 7 weeks on Balb/c mice, it raised no measurable response unless associated to UDL or UDA. The highest systemic response, IgGa2 mediated, 1 log lower than im dsLp Al(2)O(3), was elicited by dsLp-UDA. Such findings suggest that in vivo, UDL and UDA acted as penetration enhancers for dsLp, but only dsLp-UDA, owed to its pronounced uptake by APC, succeeded as topical adjuvants. The actual TPL composition, fully made of sn2,3 ether linked saturated archaeolipids, gives the UDA bilayer resistance against chemical, physical and enzymatic attacks that destroy ordinary phospholipids bilayers. Together, these properties make UDA a promising platform for topical drug targeted delivery and vaccination, that may be of help for countries with a deficient healthcare system.
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spelling pubmed-47749282016-03-10 Ultradeformable Archaeosomes for Needle Free Nanovaccination with Leishmania braziliensis Antigens Higa, Leticia H. Arnal, Laura Vermeulen, Mónica Perez, Ana Paula Schilrreff, Priscila Mundiña-Weilenmann, Cecilia Yantorno, Osvaldo Vela, María Elena Morilla, María José Romero, Eder Lilia PLoS One Research Article Total antigens from Leishmania braziliensis promastigotes, solubilized with sodium cholate (dsLp), were formulated within ultradeformable nanovesicles (dsLp-ultradeformable archaeosomes, (dsLp-UDA), and dsLp-ultradeformable liposomes (dsLp-UDL)) and topically administered to Balb/c mice. Ultradeformable nanovesicles can penetrate the intact stratum corneum up to the viable epidermis, with no aid of classical permeation enhancers that can damage the barrier function of the skin. Briefly, 100 nm unilamellar dsLp-UDA (soybean phosphatidylcholine: Halorubrum tebenquichense total polar lipids (TPL): sodium cholate, 3:3:1 w:w) of -31.45 mV Z potential, containing 4.84 ± 0.53% w/w protein/lipid dsLp, 235 KPa Young modulus were prepared. In vitro, dsLp-UDA was extensively taken up by J774A1 and bone marrow derive cells, and the only that induced an immediate secretion of IL-6, IL-12p40 and TNF-α, followed by IL-1β, by J774A1 cells. Such extensive uptake is a key feature of UDA ascribed to the highly negatively charged archaeolipids of the TPL, which are recognized by a receptor specialized in uptake and not involved in downstream signaling. Despite dsLp alone was also immunostimulatory on J774A1 cells, applied twice a week on consecutive days along 7 weeks on Balb/c mice, it raised no measurable response unless associated to UDL or UDA. The highest systemic response, IgGa2 mediated, 1 log lower than im dsLp Al(2)O(3), was elicited by dsLp-UDA. Such findings suggest that in vivo, UDL and UDA acted as penetration enhancers for dsLp, but only dsLp-UDA, owed to its pronounced uptake by APC, succeeded as topical adjuvants. The actual TPL composition, fully made of sn2,3 ether linked saturated archaeolipids, gives the UDA bilayer resistance against chemical, physical and enzymatic attacks that destroy ordinary phospholipids bilayers. Together, these properties make UDA a promising platform for topical drug targeted delivery and vaccination, that may be of help for countries with a deficient healthcare system. Public Library of Science 2016-03-02 /pmc/articles/PMC4774928/ /pubmed/26934726 http://dx.doi.org/10.1371/journal.pone.0150185 Text en © 2016 Higa et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Higa, Leticia H.
Arnal, Laura
Vermeulen, Mónica
Perez, Ana Paula
Schilrreff, Priscila
Mundiña-Weilenmann, Cecilia
Yantorno, Osvaldo
Vela, María Elena
Morilla, María José
Romero, Eder Lilia
Ultradeformable Archaeosomes for Needle Free Nanovaccination with Leishmania braziliensis Antigens
title Ultradeformable Archaeosomes for Needle Free Nanovaccination with Leishmania braziliensis Antigens
title_full Ultradeformable Archaeosomes for Needle Free Nanovaccination with Leishmania braziliensis Antigens
title_fullStr Ultradeformable Archaeosomes for Needle Free Nanovaccination with Leishmania braziliensis Antigens
title_full_unstemmed Ultradeformable Archaeosomes for Needle Free Nanovaccination with Leishmania braziliensis Antigens
title_short Ultradeformable Archaeosomes for Needle Free Nanovaccination with Leishmania braziliensis Antigens
title_sort ultradeformable archaeosomes for needle free nanovaccination with leishmania braziliensis antigens
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4774928/
https://www.ncbi.nlm.nih.gov/pubmed/26934726
http://dx.doi.org/10.1371/journal.pone.0150185
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