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In vivo study of the GC90/IRIV vaccine for immune response and autoimmunity into a novel humanised transgenic mouse
Parathyroid hormone-related protein (PTH-rP), a secreted protein produced by prostate carcinoma and other epithelial cancers, is considered a key agent for the development of bone metastases. We investigated the construct GC90/IRIV, composed of immunopotentiating reconstituted influenza virosomes (I...
Autores principales: | , , , , , , , , , , , |
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Formato: | Texto |
Lenguaje: | English |
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Nature Publishing Group
2003
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394210/ https://www.ncbi.nlm.nih.gov/pubmed/12838324 http://dx.doi.org/10.1038/sj.bjc.6601028 |
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author | Scardino, A Correale, P Firat, H Pellegrini, M Kosmatopoulos, K Opolon, P Alves, P Zurbriggen, R Glück, R Lemonnier, F A Francini, G Cusi, M G |
author_facet | Scardino, A Correale, P Firat, H Pellegrini, M Kosmatopoulos, K Opolon, P Alves, P Zurbriggen, R Glück, R Lemonnier, F A Francini, G Cusi, M G |
author_sort | Scardino, A |
collection | PubMed |
description | Parathyroid hormone-related protein (PTH-rP), a secreted protein produced by prostate carcinoma and other epithelial cancers, is considered a key agent for the development of bone metastases. We investigated the construct GC90/IRIV, composed of immunopotentiating reconstituted influenza virosomes (IRIV) containing PTH-rP gene plasmids (GC90), as a potential tool for human anticancer immunotherapy into humanised mice transgenic for HLA-A((*))02.01, the human-β2 microglobulin, and the human CD8α molecule. Intranasal administration of GC90/IRIV resulted in the induction of a PTH-rP-specific multiepitope cytotoxic T-cell (CTL) response. Cytotoxic T cells derived from vaccinated mice were capable of lysing in vitro syngenic murine PTH-rP transfectants and human HLA-A((*))02.01(+)/PTH-rP(+) prostate carcinoma LNCaP cells as well. The immune response capacity and the absence of any sign of toxicity and/or autoimmunity in vivo suggest the GC90/IRIV vaccine as a valid tool for active specific immunotherapy of human cancers and metastases overexpressing PTH-rP. |
format | Text |
id | pubmed-2394210 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2003 |
publisher | Nature Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-23942102009-09-10 In vivo study of the GC90/IRIV vaccine for immune response and autoimmunity into a novel humanised transgenic mouse Scardino, A Correale, P Firat, H Pellegrini, M Kosmatopoulos, K Opolon, P Alves, P Zurbriggen, R Glück, R Lemonnier, F A Francini, G Cusi, M G Br J Cancer Experimental Therapeutics Parathyroid hormone-related protein (PTH-rP), a secreted protein produced by prostate carcinoma and other epithelial cancers, is considered a key agent for the development of bone metastases. We investigated the construct GC90/IRIV, composed of immunopotentiating reconstituted influenza virosomes (IRIV) containing PTH-rP gene plasmids (GC90), as a potential tool for human anticancer immunotherapy into humanised mice transgenic for HLA-A((*))02.01, the human-β2 microglobulin, and the human CD8α molecule. Intranasal administration of GC90/IRIV resulted in the induction of a PTH-rP-specific multiepitope cytotoxic T-cell (CTL) response. Cytotoxic T cells derived from vaccinated mice were capable of lysing in vitro syngenic murine PTH-rP transfectants and human HLA-A((*))02.01(+)/PTH-rP(+) prostate carcinoma LNCaP cells as well. The immune response capacity and the absence of any sign of toxicity and/or autoimmunity in vivo suggest the GC90/IRIV vaccine as a valid tool for active specific immunotherapy of human cancers and metastases overexpressing PTH-rP. Nature Publishing Group 2003-07-07 2003-07-01 /pmc/articles/PMC2394210/ /pubmed/12838324 http://dx.doi.org/10.1038/sj.bjc.6601028 Text en Copyright © 2003 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Experimental Therapeutics Scardino, A Correale, P Firat, H Pellegrini, M Kosmatopoulos, K Opolon, P Alves, P Zurbriggen, R Glück, R Lemonnier, F A Francini, G Cusi, M G In vivo study of the GC90/IRIV vaccine for immune response and autoimmunity into a novel humanised transgenic mouse |
title | In vivo study of the GC90/IRIV vaccine for immune response and autoimmunity into a novel humanised transgenic mouse |
title_full | In vivo study of the GC90/IRIV vaccine for immune response and autoimmunity into a novel humanised transgenic mouse |
title_fullStr | In vivo study of the GC90/IRIV vaccine for immune response and autoimmunity into a novel humanised transgenic mouse |
title_full_unstemmed | In vivo study of the GC90/IRIV vaccine for immune response and autoimmunity into a novel humanised transgenic mouse |
title_short | In vivo study of the GC90/IRIV vaccine for immune response and autoimmunity into a novel humanised transgenic mouse |
title_sort | in vivo study of the gc90/iriv vaccine for immune response and autoimmunity into a novel humanised transgenic mouse |
topic | Experimental Therapeutics |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2394210/ https://www.ncbi.nlm.nih.gov/pubmed/12838324 http://dx.doi.org/10.1038/sj.bjc.6601028 |
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