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Cancer vaccines

Cancer vaccines are designed to promote tumor specific immune responses, particularly cytotoxic CD8 positive T cells that are specific to tumor antigens. The earliest vaccines, which were developed in 1994-95, tested non-mutated, shared tumor associated antigens that had been shown to be immunogenic...

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Detalles Bibliográficos
Autor principal: Butterfield, Lisa H
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group Ltd. 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707521/
https://www.ncbi.nlm.nih.gov/pubmed/25904595
http://dx.doi.org/10.1136/bmj.h988
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author Butterfield, Lisa H
author_facet Butterfield, Lisa H
author_sort Butterfield, Lisa H
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description Cancer vaccines are designed to promote tumor specific immune responses, particularly cytotoxic CD8 positive T cells that are specific to tumor antigens. The earliest vaccines, which were developed in 1994-95, tested non-mutated, shared tumor associated antigens that had been shown to be immunogenic and capable of inducing clinical responses in a minority of people with late stage cancer. Technological developments in the past few years have enabled the investigation of vaccines that target mutated antigens that are patient specific. Several platforms for cancer vaccination are being tested, including peptides, proteins, antigen presenting cells, tumor cells, and viral vectors. Standard of care treatments, such as surgery and ablation, chemotherapy, and radiotherapy, can also induce antitumor immunity, thereby having cancer vaccine effects. The monitoring of patients’ immune responses at baseline and after standard of care treatment is shedding light on immune biomarkers. Combination therapies are being tested in clinical trials and are likely to be the best approach to improving patient outcomes.
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spelling pubmed-47075212016-01-13 Cancer vaccines Butterfield, Lisa H BMJ Clinical Review Cancer vaccines are designed to promote tumor specific immune responses, particularly cytotoxic CD8 positive T cells that are specific to tumor antigens. The earliest vaccines, which were developed in 1994-95, tested non-mutated, shared tumor associated antigens that had been shown to be immunogenic and capable of inducing clinical responses in a minority of people with late stage cancer. Technological developments in the past few years have enabled the investigation of vaccines that target mutated antigens that are patient specific. Several platforms for cancer vaccination are being tested, including peptides, proteins, antigen presenting cells, tumor cells, and viral vectors. Standard of care treatments, such as surgery and ablation, chemotherapy, and radiotherapy, can also induce antitumor immunity, thereby having cancer vaccine effects. The monitoring of patients’ immune responses at baseline and after standard of care treatment is shedding light on immune biomarkers. Combination therapies are being tested in clinical trials and are likely to be the best approach to improving patient outcomes. BMJ Publishing Group Ltd. 2015-04-22 /pmc/articles/PMC4707521/ /pubmed/25904595 http://dx.doi.org/10.1136/bmj.h988 Text en © BMJ Publishing Group Ltd 2015
spellingShingle Clinical Review
Butterfield, Lisa H
Cancer vaccines
title Cancer vaccines
title_full Cancer vaccines
title_fullStr Cancer vaccines
title_full_unstemmed Cancer vaccines
title_short Cancer vaccines
title_sort cancer vaccines
topic Clinical Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4707521/
https://www.ncbi.nlm.nih.gov/pubmed/25904595
http://dx.doi.org/10.1136/bmj.h988
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