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Cancer immunotherapies targeting the PD-1 signaling pathway
Immunotherapy has recently emerged as the fourth pillar of cancer treatment, joining surgery, radiation, and chemotherapy. While early immunotherapies focused on accelerating T-cell activity, current immune-checkpoint inhibitors take the brakes off the anti-tumor immune responses. Successful clinica...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381059/ https://www.ncbi.nlm.nih.gov/pubmed/28376884 http://dx.doi.org/10.1186/s12929-017-0329-9 |
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author | Iwai, Yoshiko Hamanishi, Junzo Chamoto, Kenji Honjo, Tasuku |
author_facet | Iwai, Yoshiko Hamanishi, Junzo Chamoto, Kenji Honjo, Tasuku |
author_sort | Iwai, Yoshiko |
collection | PubMed |
description | Immunotherapy has recently emerged as the fourth pillar of cancer treatment, joining surgery, radiation, and chemotherapy. While early immunotherapies focused on accelerating T-cell activity, current immune-checkpoint inhibitors take the brakes off the anti-tumor immune responses. Successful clinical trials with PD-1 monoclonal antibodies and other immune-checkpoint inhibitors have opened new avenues in cancer immunology. However, the failure of a large subset of cancer patients to respond to these new immunotherapies has led to intensified research on combination therapies and predictive biomarkers. Here we summarize the development of PD-1-blockade immunotherapy and current issues in its clinical use. |
format | Online Article Text |
id | pubmed-5381059 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-53810592017-04-10 Cancer immunotherapies targeting the PD-1 signaling pathway Iwai, Yoshiko Hamanishi, Junzo Chamoto, Kenji Honjo, Tasuku J Biomed Sci Review Immunotherapy has recently emerged as the fourth pillar of cancer treatment, joining surgery, radiation, and chemotherapy. While early immunotherapies focused on accelerating T-cell activity, current immune-checkpoint inhibitors take the brakes off the anti-tumor immune responses. Successful clinical trials with PD-1 monoclonal antibodies and other immune-checkpoint inhibitors have opened new avenues in cancer immunology. However, the failure of a large subset of cancer patients to respond to these new immunotherapies has led to intensified research on combination therapies and predictive biomarkers. Here we summarize the development of PD-1-blockade immunotherapy and current issues in its clinical use. BioMed Central 2017-04-04 /pmc/articles/PMC5381059/ /pubmed/28376884 http://dx.doi.org/10.1186/s12929-017-0329-9 Text en © The Author(s). 2017 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Review Iwai, Yoshiko Hamanishi, Junzo Chamoto, Kenji Honjo, Tasuku Cancer immunotherapies targeting the PD-1 signaling pathway |
title | Cancer immunotherapies targeting the PD-1 signaling pathway |
title_full | Cancer immunotherapies targeting the PD-1 signaling pathway |
title_fullStr | Cancer immunotherapies targeting the PD-1 signaling pathway |
title_full_unstemmed | Cancer immunotherapies targeting the PD-1 signaling pathway |
title_short | Cancer immunotherapies targeting the PD-1 signaling pathway |
title_sort | cancer immunotherapies targeting the pd-1 signaling pathway |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5381059/ https://www.ncbi.nlm.nih.gov/pubmed/28376884 http://dx.doi.org/10.1186/s12929-017-0329-9 |
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