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Cancer immunotherapy: avoiding the road to perdition
The hypothesis that human cancers express antigens that can be specifically targeted by cell mediated immunity has become a scientifically justifiable rationale for the design and clinical testing of novel tumor-associated antigens (TAA). Although a number of TAA have been recognized and it has been...
Autores principales: | , , , |
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Formato: | Texto |
Lenguaje: | English |
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BioMed Central
2004
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC509287/ https://www.ncbi.nlm.nih.gov/pubmed/15283862 http://dx.doi.org/10.1186/1479-5876-2-26 |
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author | Chiriva-Internati, Maurizio Grizzi, Fabio Bright, Robert K Martin Kast, W |
author_facet | Chiriva-Internati, Maurizio Grizzi, Fabio Bright, Robert K Martin Kast, W |
author_sort | Chiriva-Internati, Maurizio |
collection | PubMed |
description | The hypothesis that human cancers express antigens that can be specifically targeted by cell mediated immunity has become a scientifically justifiable rationale for the design and clinical testing of novel tumor-associated antigens (TAA). Although a number of TAA have been recognized and it has been suggested that they could be useful in the immunological treatment of cancer, the complexity of human beings leads us to reflect on the need to establish new criteria for validating their real applicability. Herein, we show a system level-based approach that includes morphological and molecular techniques, which is specifically required to improve the capacity to produce desired results and to allow cancer immunotherapy to re-emerge from the mist in which it is currently shrouded. |
format | Text |
id | pubmed-509287 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2004 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-5092872004-08-13 Cancer immunotherapy: avoiding the road to perdition Chiriva-Internati, Maurizio Grizzi, Fabio Bright, Robert K Martin Kast, W J Transl Med Commentary The hypothesis that human cancers express antigens that can be specifically targeted by cell mediated immunity has become a scientifically justifiable rationale for the design and clinical testing of novel tumor-associated antigens (TAA). Although a number of TAA have been recognized and it has been suggested that they could be useful in the immunological treatment of cancer, the complexity of human beings leads us to reflect on the need to establish new criteria for validating their real applicability. Herein, we show a system level-based approach that includes morphological and molecular techniques, which is specifically required to improve the capacity to produce desired results and to allow cancer immunotherapy to re-emerge from the mist in which it is currently shrouded. BioMed Central 2004-07-29 /pmc/articles/PMC509287/ /pubmed/15283862 http://dx.doi.org/10.1186/1479-5876-2-26 Text en Copyright © 2004 Chiriva-Internati et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an open-access article distributed under the terms of the Creative Commons Attribution License ( (http://creativecommons.org/licenses/by/2.0) ), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Commentary Chiriva-Internati, Maurizio Grizzi, Fabio Bright, Robert K Martin Kast, W Cancer immunotherapy: avoiding the road to perdition |
title | Cancer immunotherapy: avoiding the road to perdition |
title_full | Cancer immunotherapy: avoiding the road to perdition |
title_fullStr | Cancer immunotherapy: avoiding the road to perdition |
title_full_unstemmed | Cancer immunotherapy: avoiding the road to perdition |
title_short | Cancer immunotherapy: avoiding the road to perdition |
title_sort | cancer immunotherapy: avoiding the road to perdition |
topic | Commentary |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC509287/ https://www.ncbi.nlm.nih.gov/pubmed/15283862 http://dx.doi.org/10.1186/1479-5876-2-26 |
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