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Broad Antigenic Coverage Induced by Viral cDNA Library-based Vaccination Cures Established Tumors
We show here that a cDNA library of normal tissue, expressed from a highly immunogenic viral platform, cures established tumors of the same histological type from which the cDNA library was derived. With suboptimal vaccination, immune escape was possible, but only when tumor cells were forced to acq...
Autores principales: | , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3918897/ https://www.ncbi.nlm.nih.gov/pubmed/21685898 http://dx.doi.org/10.1038/nm.2390 |
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author | Kottke, Timothy Errington, Fiona Pulido, Jose Galivo, Feorillo Thompson, Jill Wongthida, Phonphimon Diaz, Rosa Maria Chong, Heung ILett, Elizabeth Chester, John Pandha, Hardev Harrington, Kevin Selby, Peter Melcher, Alan Vile, Richard |
author_facet | Kottke, Timothy Errington, Fiona Pulido, Jose Galivo, Feorillo Thompson, Jill Wongthida, Phonphimon Diaz, Rosa Maria Chong, Heung ILett, Elizabeth Chester, John Pandha, Hardev Harrington, Kevin Selby, Peter Melcher, Alan Vile, Richard |
author_sort | Kottke, Timothy |
collection | PubMed |
description | We show here that a cDNA library of normal tissue, expressed from a highly immunogenic viral platform, cures established tumors of the same histological type from which the cDNA library was derived. With suboptimal vaccination, immune escape was possible, but only when tumor cells were forced to acquire a radically new phenotype, readily treated by second line therapy. This approach has several major advantages. Use of the cDNA library leads to presentation of a broad repertoire of (undefined) tumor associated antigens, which reduces emergence of treatment resistant variants and also permits implementation of rational, combined modality approaches in the clinic. Finally, the viral vectors can be delivered systemically, without the need for tumor targeting, and are amenable to clinical grade production. Therefore, virus-expressed cDNA libraries represent a novel paradigm for cancer treatment by addressing many of the key issues which have undermined the efficacy of immuno/virotherapy to date. |
format | Online Article Text |
id | pubmed-3918897 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
record_format | MEDLINE/PubMed |
spelling | pubmed-39188972014-02-10 Broad Antigenic Coverage Induced by Viral cDNA Library-based Vaccination Cures Established Tumors Kottke, Timothy Errington, Fiona Pulido, Jose Galivo, Feorillo Thompson, Jill Wongthida, Phonphimon Diaz, Rosa Maria Chong, Heung ILett, Elizabeth Chester, John Pandha, Hardev Harrington, Kevin Selby, Peter Melcher, Alan Vile, Richard Nat Med Article We show here that a cDNA library of normal tissue, expressed from a highly immunogenic viral platform, cures established tumors of the same histological type from which the cDNA library was derived. With suboptimal vaccination, immune escape was possible, but only when tumor cells were forced to acquire a radically new phenotype, readily treated by second line therapy. This approach has several major advantages. Use of the cDNA library leads to presentation of a broad repertoire of (undefined) tumor associated antigens, which reduces emergence of treatment resistant variants and also permits implementation of rational, combined modality approaches in the clinic. Finally, the viral vectors can be delivered systemically, without the need for tumor targeting, and are amenable to clinical grade production. Therefore, virus-expressed cDNA libraries represent a novel paradigm for cancer treatment by addressing many of the key issues which have undermined the efficacy of immuno/virotherapy to date. 2011-06-19 /pmc/articles/PMC3918897/ /pubmed/21685898 http://dx.doi.org/10.1038/nm.2390 Text en Users may view, print, copy, download and text and data- mine the content in such documents, for the purposes of academic research, subject always to the full Conditions of use: http://www.nature.com/authors/editorial_policies/license.html#terms |
spellingShingle | Article Kottke, Timothy Errington, Fiona Pulido, Jose Galivo, Feorillo Thompson, Jill Wongthida, Phonphimon Diaz, Rosa Maria Chong, Heung ILett, Elizabeth Chester, John Pandha, Hardev Harrington, Kevin Selby, Peter Melcher, Alan Vile, Richard Broad Antigenic Coverage Induced by Viral cDNA Library-based Vaccination Cures Established Tumors |
title | Broad Antigenic Coverage Induced by Viral cDNA Library-based Vaccination Cures Established Tumors |
title_full | Broad Antigenic Coverage Induced by Viral cDNA Library-based Vaccination Cures Established Tumors |
title_fullStr | Broad Antigenic Coverage Induced by Viral cDNA Library-based Vaccination Cures Established Tumors |
title_full_unstemmed | Broad Antigenic Coverage Induced by Viral cDNA Library-based Vaccination Cures Established Tumors |
title_short | Broad Antigenic Coverage Induced by Viral cDNA Library-based Vaccination Cures Established Tumors |
title_sort | broad antigenic coverage induced by viral cdna library-based vaccination cures established tumors |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3918897/ https://www.ncbi.nlm.nih.gov/pubmed/21685898 http://dx.doi.org/10.1038/nm.2390 |
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