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Potential of an anti-bevacizumab idiotype scFv DNA-based immunization to elicit VEGF-binding antibody response
Anti-idiotype antibodies have been considered for vaccination approaches against different diseases, including cancers. Based on that, we previously described an anti-bevacizumab idiotype monoclonal antibody, 10.D7, that revealed detectable antitumor effects on a vascular endothelial growth factor (...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9734904/ https://www.ncbi.nlm.nih.gov/pubmed/36482074 http://dx.doi.org/10.1038/s41434-022-00376-9 |
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author | Silva, Tábata Almeida Aguiar, Rodrigo Barbosa Mori, Marcelo Machado, Gabriel Esquitini Hamaguchi, Barbara Machado, Marcelo Ferreira Marcondes Moraes, Jane Zveiter |
author_facet | Silva, Tábata Almeida Aguiar, Rodrigo Barbosa Mori, Marcelo Machado, Gabriel Esquitini Hamaguchi, Barbara Machado, Marcelo Ferreira Marcondes Moraes, Jane Zveiter |
author_sort | Silva, Tábata Almeida |
collection | PubMed |
description | Anti-idiotype antibodies have been considered for vaccination approaches against different diseases, including cancers. Based on that, we previously described an anti-bevacizumab idiotype monoclonal antibody, 10.D7, that revealed detectable antitumor effects on a vascular endothelial growth factor (VEGF)-dependent tumor model. Herein, we evaluated the possible applicability of a single-chain variable fragment (scFv) for the 10.D7 antibody in a gene immunization strategy. After checking that mammalian cells transfected to express the 10.D7 scFv are recognized by bevacizumab, it was explored the ability of our scFv construction, in a gene-based scheme, to elicit an immune response containing VEGF-binding antibodies. The results provide evidence that the designed 10.D7 scFv construct maintains the anti-bevacizumab idiotype features and has potential to activate an immune response recognizing VEGF. |
format | Online Article Text |
id | pubmed-9734904 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-97349042022-12-12 Potential of an anti-bevacizumab idiotype scFv DNA-based immunization to elicit VEGF-binding antibody response Silva, Tábata Almeida Aguiar, Rodrigo Barbosa Mori, Marcelo Machado, Gabriel Esquitini Hamaguchi, Barbara Machado, Marcelo Ferreira Marcondes Moraes, Jane Zveiter Gene Ther Brief Communication Anti-idiotype antibodies have been considered for vaccination approaches against different diseases, including cancers. Based on that, we previously described an anti-bevacizumab idiotype monoclonal antibody, 10.D7, that revealed detectable antitumor effects on a vascular endothelial growth factor (VEGF)-dependent tumor model. Herein, we evaluated the possible applicability of a single-chain variable fragment (scFv) for the 10.D7 antibody in a gene immunization strategy. After checking that mammalian cells transfected to express the 10.D7 scFv are recognized by bevacizumab, it was explored the ability of our scFv construction, in a gene-based scheme, to elicit an immune response containing VEGF-binding antibodies. The results provide evidence that the designed 10.D7 scFv construct maintains the anti-bevacizumab idiotype features and has potential to activate an immune response recognizing VEGF. Nature Publishing Group UK 2022-12-08 /pmc/articles/PMC9734904/ /pubmed/36482074 http://dx.doi.org/10.1038/s41434-022-00376-9 Text en © The Author(s), under exclusive licence to Springer Nature Limited 2022, Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law. This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Brief Communication Silva, Tábata Almeida Aguiar, Rodrigo Barbosa Mori, Marcelo Machado, Gabriel Esquitini Hamaguchi, Barbara Machado, Marcelo Ferreira Marcondes Moraes, Jane Zveiter Potential of an anti-bevacizumab idiotype scFv DNA-based immunization to elicit VEGF-binding antibody response |
title | Potential of an anti-bevacizumab idiotype scFv DNA-based immunization to elicit VEGF-binding antibody response |
title_full | Potential of an anti-bevacizumab idiotype scFv DNA-based immunization to elicit VEGF-binding antibody response |
title_fullStr | Potential of an anti-bevacizumab idiotype scFv DNA-based immunization to elicit VEGF-binding antibody response |
title_full_unstemmed | Potential of an anti-bevacizumab idiotype scFv DNA-based immunization to elicit VEGF-binding antibody response |
title_short | Potential of an anti-bevacizumab idiotype scFv DNA-based immunization to elicit VEGF-binding antibody response |
title_sort | potential of an anti-bevacizumab idiotype scfv dna-based immunization to elicit vegf-binding antibody response |
topic | Brief Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9734904/ https://www.ncbi.nlm.nih.gov/pubmed/36482074 http://dx.doi.org/10.1038/s41434-022-00376-9 |
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