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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...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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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. |
format | Online Article Text |
id | pubmed-3238287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
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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