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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...

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Autores principales: 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
Formato: Texto
Lenguaje:English
Publicado: Nature Publishing Group 2003
Materias:
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.
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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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