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Challenges to the development of antigen-specific breast cancer vaccines

Continued progress in the development of antigen-specific breast cancer vaccines depends on the identification of appropriate target antigens, the establishment of effective immunization strategies, and the ability to circumvent immune escape mechanisms. Methods such as T cell epitope cloning and se...

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Detalles Bibliográficos
Autores principales: Scanlan, Matthew J, Jäger, Dirk
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2001
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC139438/
https://www.ncbi.nlm.nih.gov/pubmed/11250753
http://dx.doi.org/10.1186/bcr278
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author Scanlan, Matthew J
Jäger, Dirk
author_facet Scanlan, Matthew J
Jäger, Dirk
author_sort Scanlan, Matthew J
collection PubMed
description Continued progress in the development of antigen-specific breast cancer vaccines depends on the identification of appropriate target antigens, the establishment of effective immunization strategies, and the ability to circumvent immune escape mechanisms. Methods such as T cell epitope cloning and serological expression cloning (SEREX) have led to the identification of a number target antigens expressed in breast cancer. Improved immunization strategies, such as using dendritic cells to present tumor-associated antigens to T lymphocytes, have been shown to induce antigen-specific T cell responses in vivo and, in some cases, objective clinical responses. An outcome of successful tumor immunity is the evolution of antigen-loss tumor variants. The development of a polyvalent breast cancer vaccine, directed against a panel of tumor-associated antigens, may counteract this form of immune escape.
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spelling pubmed-1394382003-02-27 Challenges to the development of antigen-specific breast cancer vaccines Scanlan, Matthew J Jäger, Dirk Breast Cancer Res Commentary Continued progress in the development of antigen-specific breast cancer vaccines depends on the identification of appropriate target antigens, the establishment of effective immunization strategies, and the ability to circumvent immune escape mechanisms. Methods such as T cell epitope cloning and serological expression cloning (SEREX) have led to the identification of a number target antigens expressed in breast cancer. Improved immunization strategies, such as using dendritic cells to present tumor-associated antigens to T lymphocytes, have been shown to induce antigen-specific T cell responses in vivo and, in some cases, objective clinical responses. An outcome of successful tumor immunity is the evolution of antigen-loss tumor variants. The development of a polyvalent breast cancer vaccine, directed against a panel of tumor-associated antigens, may counteract this form of immune escape. BioMed Central 2001 2001-01-11 /pmc/articles/PMC139438/ /pubmed/11250753 http://dx.doi.org/10.1186/bcr278 Text en Copyright © 2001 BioMed Central Ltd
spellingShingle Commentary
Scanlan, Matthew J
Jäger, Dirk
Challenges to the development of antigen-specific breast cancer vaccines
title Challenges to the development of antigen-specific breast cancer vaccines
title_full Challenges to the development of antigen-specific breast cancer vaccines
title_fullStr Challenges to the development of antigen-specific breast cancer vaccines
title_full_unstemmed Challenges to the development of antigen-specific breast cancer vaccines
title_short Challenges to the development of antigen-specific breast cancer vaccines
title_sort challenges to the development of antigen-specific breast cancer vaccines
topic Commentary
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC139438/
https://www.ncbi.nlm.nih.gov/pubmed/11250753
http://dx.doi.org/10.1186/bcr278
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