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Racotumomab: an anti-idiotype vaccine related to N-glycolyl-containing gangliosides – preclinical and clinical data
Neu-glycolyl (NeuGc)-containing gangliosides are attractive targets for immunotherapy with anti-idiotype mAbs, because these glycolipids are not normal components of the cytoplasmic membrane in humans, but their expression has been demonstrated in several human malignant tumors. Racotumomab is an an...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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Frontiers Media S.A.
2012
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3478665/ https://www.ncbi.nlm.nih.gov/pubmed/23110257 http://dx.doi.org/10.3389/fonc.2012.00150 |
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author | Vázquez, Ana M. Hernández, Ana M. Macías, Amparo Montero, Enrique Gómez, Daniel E. Alonso, Daniel F. Gabri, Mariano R. Gómez, Roberto E. |
author_facet | Vázquez, Ana M. Hernández, Ana M. Macías, Amparo Montero, Enrique Gómez, Daniel E. Alonso, Daniel F. Gabri, Mariano R. Gómez, Roberto E. |
author_sort | Vázquez, Ana M. |
collection | PubMed |
description | Neu-glycolyl (NeuGc)-containing gangliosides are attractive targets for immunotherapy with anti-idiotype mAbs, because these glycolipids are not normal components of the cytoplasmic membrane in humans, but their expression has been demonstrated in several human malignant tumors. Racotumomab is an anti-idiotype mAb specific to P3 mAb, an antibody which reacts to NeuGc-containing gangliosides, sulfatides, and other antigens expressed in tumors. Preparations containing racotumomab were able to induce a strong anti-metastatic effect in tumor-bearing mice. Different Phase I clinical trials have been conducted in patients with advanced melanoma, breast cancer, and lung cancer. The results of these clinical trials demonstrated the low toxicity and the high immunogenicity of this vaccine. The induced antibodies recognized and directly killed tumor cells expressing NeuGcGM3. A Phase II/III multicenter, controlled, randomized, double blind clinical trial was conducted to evaluate the effect of aluminum hydroxide-precipitated racotumomab vaccine in overall survival in patients with advanced non-small cell lung cancer. The clinical results of this study showed a significant clinical benefit in the patients who were treated with the anti-idiotype vaccine. |
format | Online Article Text |
id | pubmed-3478665 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2012 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-34786652012-10-29 Racotumomab: an anti-idiotype vaccine related to N-glycolyl-containing gangliosides – preclinical and clinical data Vázquez, Ana M. Hernández, Ana M. Macías, Amparo Montero, Enrique Gómez, Daniel E. Alonso, Daniel F. Gabri, Mariano R. Gómez, Roberto E. Front Oncol Immunology Neu-glycolyl (NeuGc)-containing gangliosides are attractive targets for immunotherapy with anti-idiotype mAbs, because these glycolipids are not normal components of the cytoplasmic membrane in humans, but their expression has been demonstrated in several human malignant tumors. Racotumomab is an anti-idiotype mAb specific to P3 mAb, an antibody which reacts to NeuGc-containing gangliosides, sulfatides, and other antigens expressed in tumors. Preparations containing racotumomab were able to induce a strong anti-metastatic effect in tumor-bearing mice. Different Phase I clinical trials have been conducted in patients with advanced melanoma, breast cancer, and lung cancer. The results of these clinical trials demonstrated the low toxicity and the high immunogenicity of this vaccine. The induced antibodies recognized and directly killed tumor cells expressing NeuGcGM3. A Phase II/III multicenter, controlled, randomized, double blind clinical trial was conducted to evaluate the effect of aluminum hydroxide-precipitated racotumomab vaccine in overall survival in patients with advanced non-small cell lung cancer. The clinical results of this study showed a significant clinical benefit in the patients who were treated with the anti-idiotype vaccine. Frontiers Media S.A. 2012-10-23 /pmc/articles/PMC3478665/ /pubmed/23110257 http://dx.doi.org/10.3389/fonc.2012.00150 Text en Copyright © Vázquez, Hernández, Macías, Montero, Gómez, Alonso, Gabri and Gómez. http://www.frontiersin.org/licenseagreement This is an openaccess article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) , which permits use, distribution and reproduction in other forums, provided the original authors and source are credited and subject to any copyright notices concerning any third-party graphics etc. |
spellingShingle | Immunology Vázquez, Ana M. Hernández, Ana M. Macías, Amparo Montero, Enrique Gómez, Daniel E. Alonso, Daniel F. Gabri, Mariano R. Gómez, Roberto E. Racotumomab: an anti-idiotype vaccine related to N-glycolyl-containing gangliosides – preclinical and clinical data |
title | Racotumomab: an anti-idiotype vaccine related to N-glycolyl-containing gangliosides – preclinical and clinical data |
title_full | Racotumomab: an anti-idiotype vaccine related to N-glycolyl-containing gangliosides – preclinical and clinical data |
title_fullStr | Racotumomab: an anti-idiotype vaccine related to N-glycolyl-containing gangliosides – preclinical and clinical data |
title_full_unstemmed | Racotumomab: an anti-idiotype vaccine related to N-glycolyl-containing gangliosides – preclinical and clinical data |
title_short | Racotumomab: an anti-idiotype vaccine related to N-glycolyl-containing gangliosides – preclinical and clinical data |
title_sort | racotumomab: an anti-idiotype vaccine related to n-glycolyl-containing gangliosides – preclinical and clinical data |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3478665/ https://www.ncbi.nlm.nih.gov/pubmed/23110257 http://dx.doi.org/10.3389/fonc.2012.00150 |
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