Ultradeformable archaeosomes for needle free nanovaccination with <i>Leishmania braziliensis</i> antigens

Autores
Higa, Leticia H.; Arnal, Laura; Vermeulen, Mónica; Perez, Ana Laura; Schilrreff, Priscila; Mundiña-Weilenmann, Cecilia; Yantorno, Osvaldo Miguel; Vela, María Elena; Morilla, María José; Romero, Eder Lilia
Año de publicación
2016
Idioma
inglés
Tipo de recurso
artículo
Estado
versión publicada
Descripción
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 Al2O3, 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.
Facultad de Ciencias Exactas
Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas
Centro de Investigaciones Cardiovasculares
Centro de Investigación y Desarrollo en Fermentaciones Industriales
Materia
Ciencias Exactas
Leishmania braziliensis
Antigens
Nanovaccination
Nivel de accesibilidad
acceso abierto
Condiciones de uso
http://creativecommons.org/licenses/by/4.0/
Repositorio
SEDICI (UNLP)
Institución
Universidad Nacional de La Plata
OAI Identificador
oai:sedici.unlp.edu.ar:10915/86666

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network_name_str SEDICI (UNLP)
spelling Ultradeformable archaeosomes for needle free nanovaccination with <i>Leishmania braziliensis</i> antigensHiga, Leticia H.Arnal, LauraVermeulen, MónicaPerez, Ana LauraSchilrreff, PriscilaMundiña-Weilenmann, CeciliaYantorno, Osvaldo MiguelVela, María ElenaMorilla, María JoséRomero, Eder LiliaCiencias ExactasLeishmania braziliensisAntigensNanovaccinationTotal antigens from <i>Leishmania braziliensis</i> 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: <i>Halorubrum tebenquichense</i> 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. <i>In vitro</i>, 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<sub>2</sub>O<sub>3</sub>, was elicited by dsLp-UDA. Such findings suggest that <i>in vivo</i>, 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.Facultad de Ciencias ExactasInstituto de Investigaciones Fisicoquímicas Teóricas y AplicadasCentro de Investigaciones CardiovascularesCentro de Investigación y Desarrollo en Fermentaciones Industriales2016info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionArticulohttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfhttp://sedici.unlp.edu.ar/handle/10915/86666enginfo:eu-repo/semantics/altIdentifier/issn/1932-6203info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0150185info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by/4.0/Creative Commons Attribution 4.0 International (CC BY 4.0)reponame:SEDICI (UNLP)instname:Universidad Nacional de La Platainstacron:UNLP2025-09-29T11:16:49Zoai:sedici.unlp.edu.ar:10915/86666Institucionalhttp://sedici.unlp.edu.ar/Universidad públicaNo correspondehttp://sedici.unlp.edu.ar/oai/snrdalira@sedici.unlp.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:13292025-09-29 11:16:49.416SEDICI (UNLP) - Universidad Nacional de La Platafalse
dc.title.none.fl_str_mv Ultradeformable archaeosomes for needle free nanovaccination with <i>Leishmania braziliensis</i> antigens
title Ultradeformable archaeosomes for needle free nanovaccination with <i>Leishmania braziliensis</i> antigens
spellingShingle Ultradeformable archaeosomes for needle free nanovaccination with <i>Leishmania braziliensis</i> antigens
Higa, Leticia H.
Ciencias Exactas
Leishmania braziliensis
Antigens
Nanovaccination
title_short Ultradeformable archaeosomes for needle free nanovaccination with <i>Leishmania braziliensis</i> antigens
title_full Ultradeformable archaeosomes for needle free nanovaccination with <i>Leishmania braziliensis</i> antigens
title_fullStr Ultradeformable archaeosomes for needle free nanovaccination with <i>Leishmania braziliensis</i> antigens
title_full_unstemmed Ultradeformable archaeosomes for needle free nanovaccination with <i>Leishmania braziliensis</i> antigens
title_sort Ultradeformable archaeosomes for needle free nanovaccination with <i>Leishmania braziliensis</i> antigens
dc.creator.none.fl_str_mv Higa, Leticia H.
Arnal, Laura
Vermeulen, Mónica
Perez, Ana Laura
Schilrreff, Priscila
Mundiña-Weilenmann, Cecilia
Yantorno, Osvaldo Miguel
Vela, María Elena
Morilla, María José
Romero, Eder Lilia
author Higa, Leticia H.
author_facet Higa, Leticia H.
Arnal, Laura
Vermeulen, Mónica
Perez, Ana Laura
Schilrreff, Priscila
Mundiña-Weilenmann, Cecilia
Yantorno, Osvaldo Miguel
Vela, María Elena
Morilla, María José
Romero, Eder Lilia
author_role author
author2 Arnal, Laura
Vermeulen, Mónica
Perez, Ana Laura
Schilrreff, Priscila
Mundiña-Weilenmann, Cecilia
Yantorno, Osvaldo Miguel
Vela, María Elena
Morilla, María José
Romero, Eder Lilia
author2_role author
author
author
author
author
author
author
author
author
dc.subject.none.fl_str_mv Ciencias Exactas
Leishmania braziliensis
Antigens
Nanovaccination
topic Ciencias Exactas
Leishmania braziliensis
Antigens
Nanovaccination
dc.description.none.fl_txt_mv Total antigens from <i>Leishmania braziliensis</i> 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: <i>Halorubrum tebenquichense</i> 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. <i>In vitro</i>, 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<sub>2</sub>O<sub>3</sub>, was elicited by dsLp-UDA. Such findings suggest that <i>in vivo</i>, 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.
Facultad de Ciencias Exactas
Instituto de Investigaciones Fisicoquímicas Teóricas y Aplicadas
Centro de Investigaciones Cardiovasculares
Centro de Investigación y Desarrollo en Fermentaciones Industriales
description Total antigens from <i>Leishmania braziliensis</i> 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: <i>Halorubrum tebenquichense</i> 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. <i>In vitro</i>, 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<sub>2</sub>O<sub>3</sub>, was elicited by dsLp-UDA. Such findings suggest that <i>in vivo</i>, 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.
publishDate 2016
dc.date.none.fl_str_mv 2016
dc.type.none.fl_str_mv info:eu-repo/semantics/article
info:eu-repo/semantics/publishedVersion
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info:eu-repo/semantics/altIdentifier/doi/10.1371/journal.pone.0150185
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eu_rights_str_mv openAccess
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Creative Commons Attribution 4.0 International (CC BY 4.0)
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