Corrigendum to “CpG-ODN formulated with a nanostructure as adjuvant for anticrotalic serum production. Studies in mice” [Toxicon 215 (2022) 28–36]
- Autores
- Fusco, Luciano S.; Pascual, María M.; Hernandez, David; Sánchez Vallecillo, María F.; Arrieta, María B.; Moron, Gabriel; Palma, Santiago; Maletto, Belkys A.; Leiva, Laura C.
- Año de publicación
- 2022
- Idioma
- español castellano
- Tipo de recurso
- artículo
- Estado
- versión publicada
- Descripción
- Fil: Fusco, Luciano S. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Química Básica y Aplicada del Nordeste Argentino; Argentina.
Fil: Fusco, Luciano S. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura; Argentina.
Fil: Pascual, María M. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas, Argentina.
Fil: Pascual, María M. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina.
Fil: Hernandez, David. Universidad Nacional del Nordeste. Facultad de Ciencias Veterinarias; Argentina.
Fil: Sánchez Vallecillo, María F. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas, Argentina.
Fil: Sánchez Vallecillo, María F. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina.
Fil: Arrieta, María B. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas Naturales y Agrimensura; Argentina.
Fil: Moron, Gabriel. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas, Argentina.
Fil: Moron, Gabriel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina.
Fil: Palma, Santiago. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina.
Fil: Palma, Santiago. Consejo Nacional de Investigaciones Científicas y Técnicas. Unidad de Investigación y Desarrollo en Tecnología Farmacéutica; Argentina.
Fil: Maletto, Belkys A. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas, Argentina.
Fil: Maletto, Belkys A. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina.
Fil: Leiva, Laura C. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Química Básica y Aplicada del Nordeste Argentino; Argentina.
Fil: Fil: Leiva, Laura C. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura.; Argentina.
Antivenom is the only safe and effective treatment to neutralize snake venom. Specific anti-venom used to treat snake bite is usually obtained from horses after hyperimmunization with crude snake venom in combination with Freund’s Adjuvant. Freund’s complete and incomplete adjuvant can cause severe local and sys- temic acute and chronic inflammation, its potentially severe inflammatory effects have led many researchers to seek alternative immunological adjuvants. CpG-ODN formulated in a 6-O-ascorbyl palmitate nanostructure (Coa-ASC16) was more efficient as adjuvant than CpG-ODN alone using ovalbumin (OVA) as an antigen model. Particularly, immunization of mice with OVA/CpG-ODN/Coa-ASC16 resulted in high OVA specific antibody titers and IFN-γ and IL-17 secretion compared to im- munization with OVA/CpG-ODN. First of all, we estimated the effect of Coa-ASC16 nanostructure preparation on venom activity. Additionally, in order to evaluate the immune response induced by this adjuvant strategy using Crotalus durissus terrificus (C. d. terrificus) venom (CdtV), we determined the titer of antibodies (IgG, IgG1 and IgG2) and their specificity. BALB/c mice were subcutaneously immunizated on days 0, 15 and 30 with CdtV/CpG-ODN/Coa-ASC16 or CdtV/Freund’s Adyuvant (complete first and incomplete-booster) (dose/mice: CdtV: 6–10 μg, CpG-ODN: 30 μg). On day 45 mice were sacrificed. The neutralizing ability of serum from animals immunized with CdtV/CpG-ODN/Coa-ASC16 or CdtV/Freund’s adjuvant was tested against PLA2 activity and lethality. In both immunized group mice, the antibody titers in plasma were high (1 × 105 ), with a similar IgG1/IgG2a ratio. The antibodies recognized phospholipase A2 and thrombin-like proteins, the main toxins from C. d. terrificus venom. Macroscopic and microscopic analysis at the site of injection of mice injected with Freund’s adjuvant showed local damage (with non-infectious abscesses) and hypertrophy of inguinal lymph nodes, whereas mice injected with CpG-ODN/Coa/ASC16 did not. Our results show that CpG-ODN/Coa- ASC16 produces a humoral response as strong and specific as Freund’s adjuvant, with minor or null local deleterious effect, demonstrating the potentiality and advisability of an alternative formulation as a new adjuvant option for future immunizations to produce C. d. terrificus antivenom. - Fuente
- Toxicon, 2022, vol. 216, p. 114.
- Materia
-
CpG-ODN
Snake venom - Nivel de accesibilidad
- acceso abierto
- Condiciones de uso
- http://creativecommons.org/licenses/by-nc-nd/2.5/ar/
- Repositorio
- Institución
- Universidad Nacional del Nordeste
- OAI Identificador
- oai:repositorio.unne.edu.ar:123456789/58048
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Corrigendum to “CpG-ODN formulated with a nanostructure as adjuvant for anticrotalic serum production. Studies in mice” [Toxicon 215 (2022) 28–36]Fusco, Luciano S.Pascual, María M.Hernandez, DavidSánchez Vallecillo, María F.Arrieta, María B.Moron, GabrielPalma, SantiagoMaletto, Belkys A.Leiva, Laura C.CpG-ODNSnake venomFil: Fusco, Luciano S. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Química Básica y Aplicada del Nordeste Argentino; Argentina.Fil: Fusco, Luciano S. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura; Argentina.Fil: Pascual, María M. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas, Argentina.Fil: Pascual, María M. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina.Fil: Hernandez, David. Universidad Nacional del Nordeste. Facultad de Ciencias Veterinarias; Argentina.Fil: Sánchez Vallecillo, María F. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas, Argentina.Fil: Sánchez Vallecillo, María F. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina.Fil: Arrieta, María B. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas Naturales y Agrimensura; Argentina.Fil: Moron, Gabriel. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas, Argentina.Fil: Moron, Gabriel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina.Fil: Palma, Santiago. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina.Fil: Palma, Santiago. Consejo Nacional de Investigaciones Científicas y Técnicas. Unidad de Investigación y Desarrollo en Tecnología Farmacéutica; Argentina.Fil: Maletto, Belkys A. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas, Argentina.Fil: Maletto, Belkys A. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina.Fil: Leiva, Laura C. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Química Básica y Aplicada del Nordeste Argentino; Argentina.Fil: Fil: Leiva, Laura C. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura.; Argentina.Antivenom is the only safe and effective treatment to neutralize snake venom. Specific anti-venom used to treat snake bite is usually obtained from horses after hyperimmunization with crude snake venom in combination with Freund’s Adjuvant. Freund’s complete and incomplete adjuvant can cause severe local and sys- temic acute and chronic inflammation, its potentially severe inflammatory effects have led many researchers to seek alternative immunological adjuvants. CpG-ODN formulated in a 6-O-ascorbyl palmitate nanostructure (Coa-ASC16) was more efficient as adjuvant than CpG-ODN alone using ovalbumin (OVA) as an antigen model. Particularly, immunization of mice with OVA/CpG-ODN/Coa-ASC16 resulted in high OVA specific antibody titers and IFN-γ and IL-17 secretion compared to im- munization with OVA/CpG-ODN. First of all, we estimated the effect of Coa-ASC16 nanostructure preparation on venom activity. Additionally, in order to evaluate the immune response induced by this adjuvant strategy using Crotalus durissus terrificus (C. d. terrificus) venom (CdtV), we determined the titer of antibodies (IgG, IgG1 and IgG2) and their specificity. BALB/c mice were subcutaneously immunizated on days 0, 15 and 30 with CdtV/CpG-ODN/Coa-ASC16 or CdtV/Freund’s Adyuvant (complete first and incomplete-booster) (dose/mice: CdtV: 6–10 μg, CpG-ODN: 30 μg). On day 45 mice were sacrificed. The neutralizing ability of serum from animals immunized with CdtV/CpG-ODN/Coa-ASC16 or CdtV/Freund’s adjuvant was tested against PLA2 activity and lethality. In both immunized group mice, the antibody titers in plasma were high (1 × 105 ), with a similar IgG1/IgG2a ratio. The antibodies recognized phospholipase A2 and thrombin-like proteins, the main toxins from C. d. terrificus venom. Macroscopic and microscopic analysis at the site of injection of mice injected with Freund’s adjuvant showed local damage (with non-infectious abscesses) and hypertrophy of inguinal lymph nodes, whereas mice injected with CpG-ODN/Coa/ASC16 did not. Our results show that CpG-ODN/Coa- ASC16 produces a humoral response as strong and specific as Freund’s adjuvant, with minor or null local deleterious effect, demonstrating the potentiality and advisability of an alternative formulation as a new adjuvant option for future immunizations to produce C. d. terrificus antivenom.Elsevier Ltd.2022-09-25info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersionhttp://purl.org/coar/resource_type/c_6501info:ar-repo/semantics/articuloapplication/pdfp. 1-1application/pdfFusco, Luciano S., et. al, 2022. Corrigendum to “CpG-ODN formulated with a nanostructure as adjuvant for anticrotalic serum production. Studies in mice” [Toxicon 215 (2022) 28–36]. Toxicon: Países BajosElsevier Ltd., p. 1-1, ISSN 0041-0101.0041-0101http://repositorio.unne.edu.ar/handle/123456789/58048Toxicon, 2022, vol. 216, p. 114.reponame:Repositorio Institucional de la Universidad Nacional del Nordeste (UNNE)instname:Universidad Nacional del Nordestespahttps://doi.org/10.1016/j.toxicon.2022.07.002https://doi.org/10.1016/j.toxicon.2022.05.045info:eu-repo/semantics/openAccesshttp://creativecommons.org/licenses/by-nc-nd/2.5/ar/Atribución-NoComercial-SinDerivadas 2.5 Argentina2025-09-29T14:30:49Zoai:repositorio.unne.edu.ar:123456789/58048instacron:UNNEInstitucionalhttp://repositorio.unne.edu.ar/Universidad públicaNo correspondehttp://repositorio.unne.edu.ar/oaiososa@bib.unne.edu.ar;sergio.alegria@unne.edu.arArgentinaNo correspondeNo correspondeNo correspondeopendoar:48712025-09-29 14:30:50.011Repositorio Institucional de la Universidad Nacional del Nordeste (UNNE) - Universidad Nacional del Nordestefalse |
dc.title.none.fl_str_mv |
Corrigendum to “CpG-ODN formulated with a nanostructure as adjuvant for anticrotalic serum production. Studies in mice” [Toxicon 215 (2022) 28–36] |
title |
Corrigendum to “CpG-ODN formulated with a nanostructure as adjuvant for anticrotalic serum production. Studies in mice” [Toxicon 215 (2022) 28–36] |
spellingShingle |
Corrigendum to “CpG-ODN formulated with a nanostructure as adjuvant for anticrotalic serum production. Studies in mice” [Toxicon 215 (2022) 28–36] Fusco, Luciano S. CpG-ODN Snake venom |
title_short |
Corrigendum to “CpG-ODN formulated with a nanostructure as adjuvant for anticrotalic serum production. Studies in mice” [Toxicon 215 (2022) 28–36] |
title_full |
Corrigendum to “CpG-ODN formulated with a nanostructure as adjuvant for anticrotalic serum production. Studies in mice” [Toxicon 215 (2022) 28–36] |
title_fullStr |
Corrigendum to “CpG-ODN formulated with a nanostructure as adjuvant for anticrotalic serum production. Studies in mice” [Toxicon 215 (2022) 28–36] |
title_full_unstemmed |
Corrigendum to “CpG-ODN formulated with a nanostructure as adjuvant for anticrotalic serum production. Studies in mice” [Toxicon 215 (2022) 28–36] |
title_sort |
Corrigendum to “CpG-ODN formulated with a nanostructure as adjuvant for anticrotalic serum production. Studies in mice” [Toxicon 215 (2022) 28–36] |
dc.creator.none.fl_str_mv |
Fusco, Luciano S. Pascual, María M. Hernandez, David Sánchez Vallecillo, María F. Arrieta, María B. Moron, Gabriel Palma, Santiago Maletto, Belkys A. Leiva, Laura C. |
author |
Fusco, Luciano S. |
author_facet |
Fusco, Luciano S. Pascual, María M. Hernandez, David Sánchez Vallecillo, María F. Arrieta, María B. Moron, Gabriel Palma, Santiago Maletto, Belkys A. Leiva, Laura C. |
author_role |
author |
author2 |
Pascual, María M. Hernandez, David Sánchez Vallecillo, María F. Arrieta, María B. Moron, Gabriel Palma, Santiago Maletto, Belkys A. Leiva, Laura C. |
author2_role |
author author author author author author author author |
dc.subject.none.fl_str_mv |
CpG-ODN Snake venom |
topic |
CpG-ODN Snake venom |
dc.description.none.fl_txt_mv |
Fil: Fusco, Luciano S. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Química Básica y Aplicada del Nordeste Argentino; Argentina. Fil: Fusco, Luciano S. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura; Argentina. Fil: Pascual, María M. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas, Argentina. Fil: Pascual, María M. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina. Fil: Hernandez, David. Universidad Nacional del Nordeste. Facultad de Ciencias Veterinarias; Argentina. Fil: Sánchez Vallecillo, María F. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas, Argentina. Fil: Sánchez Vallecillo, María F. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina. Fil: Arrieta, María B. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas Naturales y Agrimensura; Argentina. Fil: Moron, Gabriel. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas, Argentina. Fil: Moron, Gabriel. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina. Fil: Palma, Santiago. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas; Argentina. Fil: Palma, Santiago. Consejo Nacional de Investigaciones Científicas y Técnicas. Unidad de Investigación y Desarrollo en Tecnología Farmacéutica; Argentina. Fil: Maletto, Belkys A. Universidad Nacional de Córdoba. Facultad de Ciencias Químicas, Argentina. Fil: Maletto, Belkys A. Consejo Nacional de Investigaciones Científicas y Técnicas. Centro de Investigaciones en Bioquímica Clínica e Inmunología; Argentina. Fil: Leiva, Laura C. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Química Básica y Aplicada del Nordeste Argentino; Argentina. Fil: Fil: Leiva, Laura C. Universidad Nacional del Nordeste. Facultad de Ciencias Exactas y Naturales y Agrimensura.; Argentina. Antivenom is the only safe and effective treatment to neutralize snake venom. Specific anti-venom used to treat snake bite is usually obtained from horses after hyperimmunization with crude snake venom in combination with Freund’s Adjuvant. Freund’s complete and incomplete adjuvant can cause severe local and sys- temic acute and chronic inflammation, its potentially severe inflammatory effects have led many researchers to seek alternative immunological adjuvants. CpG-ODN formulated in a 6-O-ascorbyl palmitate nanostructure (Coa-ASC16) was more efficient as adjuvant than CpG-ODN alone using ovalbumin (OVA) as an antigen model. Particularly, immunization of mice with OVA/CpG-ODN/Coa-ASC16 resulted in high OVA specific antibody titers and IFN-γ and IL-17 secretion compared to im- munization with OVA/CpG-ODN. First of all, we estimated the effect of Coa-ASC16 nanostructure preparation on venom activity. Additionally, in order to evaluate the immune response induced by this adjuvant strategy using Crotalus durissus terrificus (C. d. terrificus) venom (CdtV), we determined the titer of antibodies (IgG, IgG1 and IgG2) and their specificity. BALB/c mice were subcutaneously immunizated on days 0, 15 and 30 with CdtV/CpG-ODN/Coa-ASC16 or CdtV/Freund’s Adyuvant (complete first and incomplete-booster) (dose/mice: CdtV: 6–10 μg, CpG-ODN: 30 μg). On day 45 mice were sacrificed. The neutralizing ability of serum from animals immunized with CdtV/CpG-ODN/Coa-ASC16 or CdtV/Freund’s adjuvant was tested against PLA2 activity and lethality. In both immunized group mice, the antibody titers in plasma were high (1 × 105 ), with a similar IgG1/IgG2a ratio. The antibodies recognized phospholipase A2 and thrombin-like proteins, the main toxins from C. d. terrificus venom. Macroscopic and microscopic analysis at the site of injection of mice injected with Freund’s adjuvant showed local damage (with non-infectious abscesses) and hypertrophy of inguinal lymph nodes, whereas mice injected with CpG-ODN/Coa/ASC16 did not. Our results show that CpG-ODN/Coa- ASC16 produces a humoral response as strong and specific as Freund’s adjuvant, with minor or null local deleterious effect, demonstrating the potentiality and advisability of an alternative formulation as a new adjuvant option for future immunizations to produce C. d. terrificus antivenom. |
description |
Fil: Fusco, Luciano S. Consejo Nacional de Investigaciones Científicas y Técnicas. Instituto de Química Básica y Aplicada del Nordeste Argentino; Argentina. |
publishDate |
2022 |
dc.date.none.fl_str_mv |
2022-09-25 |
dc.type.none.fl_str_mv |
info:eu-repo/semantics/article info:eu-repo/semantics/publishedVersion http://purl.org/coar/resource_type/c_6501 info:ar-repo/semantics/articulo |
format |
article |
status_str |
publishedVersion |
dc.identifier.none.fl_str_mv |
Fusco, Luciano S., et. al, 2022. Corrigendum to “CpG-ODN formulated with a nanostructure as adjuvant for anticrotalic serum production. Studies in mice” [Toxicon 215 (2022) 28–36]. Toxicon: Países BajosElsevier Ltd., p. 1-1, ISSN 0041-0101. 0041-0101 http://repositorio.unne.edu.ar/handle/123456789/58048 |
identifier_str_mv |
Fusco, Luciano S., et. al, 2022. Corrigendum to “CpG-ODN formulated with a nanostructure as adjuvant for anticrotalic serum production. Studies in mice” [Toxicon 215 (2022) 28–36]. Toxicon: Países BajosElsevier Ltd., p. 1-1, ISSN 0041-0101. 0041-0101 |
url |
http://repositorio.unne.edu.ar/handle/123456789/58048 |
dc.language.none.fl_str_mv |
spa |
language |
spa |
dc.relation.none.fl_str_mv |
https://doi.org/10.1016/j.toxicon.2022.07.002 https://doi.org/10.1016/j.toxicon.2022.05.045 |
dc.rights.none.fl_str_mv |
info:eu-repo/semantics/openAccess http://creativecommons.org/licenses/by-nc-nd/2.5/ar/ Atribución-NoComercial-SinDerivadas 2.5 Argentina |
eu_rights_str_mv |
openAccess |
rights_invalid_str_mv |
http://creativecommons.org/licenses/by-nc-nd/2.5/ar/ Atribución-NoComercial-SinDerivadas 2.5 Argentina |
dc.format.none.fl_str_mv |
application/pdf p. 1-1 application/pdf |
dc.publisher.none.fl_str_mv |
Elsevier Ltd. |
publisher.none.fl_str_mv |
Elsevier Ltd. |
dc.source.none.fl_str_mv |
Toxicon, 2022, vol. 216, p. 114. reponame:Repositorio Institucional de la Universidad Nacional del Nordeste (UNNE) instname:Universidad Nacional del Nordeste |
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Repositorio Institucional de la Universidad Nacional del Nordeste (UNNE) |
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Repositorio Institucional de la Universidad Nacional del Nordeste (UNNE) |
instname_str |
Universidad Nacional del Nordeste |
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Repositorio Institucional de la Universidad Nacional del Nordeste (UNNE) - Universidad Nacional del Nordeste |
repository.mail.fl_str_mv |
ososa@bib.unne.edu.ar;sergio.alegria@unne.edu.ar |
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