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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2016
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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. |
format | Online Article Text |
id | pubmed-4774928 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
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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