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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...

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Detalles Bibliográficos
Autores principales: Chiriva-Internati, Maurizio, Grizzi, Fabio, Bright, Robert K, Martin Kast, W
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2004
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.
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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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