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Physicochemical and biological characterization of 1E10 Anti-Idiotype vaccine

BACKGROUND: 1E10 monoclonal antibody is a murine anti-idiotypic antibody that mimics N-glycolyl-GM3 gangliosides. This antibody has been tested as an anti-idiotypic cancer vaccine, adjuvated in Al(OH)(3), in several clinical trials for melanoma, breast, and lung cancer. During early clinical develop...

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Detalles Bibliográficos
Autores principales: Machado, Yoan J, Rabasa, Yamilet, Montesinos, Raquel, Cremata, José, Besada, Vladimir, Fuentes, Dasha, Castillo, Adolfo, de la Luz, Kathya R, Vázquez, Ana M, Himly, Martin
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238287/
https://www.ncbi.nlm.nih.gov/pubmed/22108317
http://dx.doi.org/10.1186/1472-6750-11-112
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author Machado, Yoan J
Rabasa, Yamilet
Montesinos, Raquel
Cremata, José
Besada, Vladimir
Fuentes, Dasha
Castillo, Adolfo
de la Luz, Kathya R
Vázquez, Ana M
Himly, Martin
author_facet Machado, Yoan J
Rabasa, Yamilet
Montesinos, Raquel
Cremata, José
Besada, Vladimir
Fuentes, Dasha
Castillo, Adolfo
de la Luz, Kathya R
Vázquez, Ana M
Himly, Martin
author_sort Machado, Yoan J
collection PubMed
description BACKGROUND: 1E10 monoclonal antibody is a murine anti-idiotypic antibody that mimics N-glycolyl-GM3 gangliosides. This antibody has been tested as an anti-idiotypic cancer vaccine, adjuvated in Al(OH)(3), in several clinical trials for melanoma, breast, and lung cancer. During early clinical development this mAb was obtained in vivo from mice ascites fluid. Currently, the production process of 1E10 is being transferred from the in vivo to a bioreactor-based method. RESULTS: Here, we present a comprehensive molecular and immunological characterization of 1E10 produced by the two different production processes in order to determine the impact of the manufacturing process in vaccine performance. We observed differences in glycosylation pattern, charge heterogeneity and structural stability between in vivo-produced 1E10 and bioreactor-obtained 1E10. Interestingly, these modifications had no significant impact on the immune responses elicited in two different animal models. CONCLUSIONS: Changes in 1E10 primary structure like glycosylation; asparagine deamidation and oxidation affected 1E10 structural stability but did not affect the immune response elicited in mice and chickens when compared to 1E10 produced in mice.
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spelling pubmed-32382872011-12-16 Physicochemical and biological characterization of 1E10 Anti-Idiotype vaccine Machado, Yoan J Rabasa, Yamilet Montesinos, Raquel Cremata, José Besada, Vladimir Fuentes, Dasha Castillo, Adolfo de la Luz, Kathya R Vázquez, Ana M Himly, Martin BMC Biotechnol Research Article BACKGROUND: 1E10 monoclonal antibody is a murine anti-idiotypic antibody that mimics N-glycolyl-GM3 gangliosides. This antibody has been tested as an anti-idiotypic cancer vaccine, adjuvated in Al(OH)(3), in several clinical trials for melanoma, breast, and lung cancer. During early clinical development this mAb was obtained in vivo from mice ascites fluid. Currently, the production process of 1E10 is being transferred from the in vivo to a bioreactor-based method. RESULTS: Here, we present a comprehensive molecular and immunological characterization of 1E10 produced by the two different production processes in order to determine the impact of the manufacturing process in vaccine performance. We observed differences in glycosylation pattern, charge heterogeneity and structural stability between in vivo-produced 1E10 and bioreactor-obtained 1E10. Interestingly, these modifications had no significant impact on the immune responses elicited in two different animal models. CONCLUSIONS: Changes in 1E10 primary structure like glycosylation; asparagine deamidation and oxidation affected 1E10 structural stability but did not affect the immune response elicited in mice and chickens when compared to 1E10 produced in mice. BioMed Central 2011-11-22 /pmc/articles/PMC3238287/ /pubmed/22108317 http://dx.doi.org/10.1186/1472-6750-11-112 Text en Copyright ©2011 Machado et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Machado, Yoan J
Rabasa, Yamilet
Montesinos, Raquel
Cremata, José
Besada, Vladimir
Fuentes, Dasha
Castillo, Adolfo
de la Luz, Kathya R
Vázquez, Ana M
Himly, Martin
Physicochemical and biological characterization of 1E10 Anti-Idiotype vaccine
title Physicochemical and biological characterization of 1E10 Anti-Idiotype vaccine
title_full Physicochemical and biological characterization of 1E10 Anti-Idiotype vaccine
title_fullStr Physicochemical and biological characterization of 1E10 Anti-Idiotype vaccine
title_full_unstemmed Physicochemical and biological characterization of 1E10 Anti-Idiotype vaccine
title_short Physicochemical and biological characterization of 1E10 Anti-Idiotype vaccine
title_sort physicochemical and biological characterization of 1e10 anti-idiotype vaccine
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3238287/
https://www.ncbi.nlm.nih.gov/pubmed/22108317
http://dx.doi.org/10.1186/1472-6750-11-112
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