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New emerging targets in cancer immunotherapy: the role of TIM3

Currently, the programmed death-1/programmed death ligand-1 and the cytotoxic T-lymphocyte-associated protein 4 are the two commonly targeted immune-checkpoint inhibition pathways. These drugs have significantly improved the prognosis of many cancer types. While immune-checkpoint inhibitors have rev...

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Detalles Bibliográficos
Autores principales: Friedlaender, Alex, Addeo, Alfredo, Banna, Giuseppe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6579568/
https://www.ncbi.nlm.nih.gov/pubmed/31275616
http://dx.doi.org/10.1136/esmoopen-2019-000497
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author Friedlaender, Alex
Addeo, Alfredo
Banna, Giuseppe
author_facet Friedlaender, Alex
Addeo, Alfredo
Banna, Giuseppe
author_sort Friedlaender, Alex
collection PubMed
description Currently, the programmed death-1/programmed death ligand-1 and the cytotoxic T-lymphocyte-associated protein 4 are the two commonly targeted immune-checkpoint inhibition pathways. These drugs have significantly improved the prognosis of many cancer types. While immune-checkpoint inhibitors have revolutionised the treatment of many cancer types, the majority of patients still progress. Several treatment strategies have been pursued to improve current results. One approach is to combine two checkpoint inhibitors, currently with promising results in melanoma, renal cell carcinoma and a subset of non-small-cell lung cancer patients. The identification of new checkpoint targets could allow the field of immuno-oncology to evolve further. We will discuss one of the most promising immune-checkpoint targets currently under investigation, the T-cell immunoglobulin and mucin domain-3.
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spelling pubmed-65795682019-07-02 New emerging targets in cancer immunotherapy: the role of TIM3 Friedlaender, Alex Addeo, Alfredo Banna, Giuseppe ESMO Open Review Currently, the programmed death-1/programmed death ligand-1 and the cytotoxic T-lymphocyte-associated protein 4 are the two commonly targeted immune-checkpoint inhibition pathways. These drugs have significantly improved the prognosis of many cancer types. While immune-checkpoint inhibitors have revolutionised the treatment of many cancer types, the majority of patients still progress. Several treatment strategies have been pursued to improve current results. One approach is to combine two checkpoint inhibitors, currently with promising results in melanoma, renal cell carcinoma and a subset of non-small-cell lung cancer patients. The identification of new checkpoint targets could allow the field of immuno-oncology to evolve further. We will discuss one of the most promising immune-checkpoint targets currently under investigation, the T-cell immunoglobulin and mucin domain-3. BMJ Publishing Group 2019-06-12 /pmc/articles/PMC6579568/ /pubmed/31275616 http://dx.doi.org/10.1136/esmoopen-2019-000497 Text en © Author (s) (or their employer(s)) 2019. Re-use permitted under CC BY. Published by BMJ on behalf of the European Society for Medical Oncology. This is an open access article distributed in accordance with the Creative Commons Attribution 4.0 Unported (CC BY 4.0) license, which permits others to copy, redistribute, remix, transform and build upon this work for any purpose, provided the original work is properly cited, a link to the licence is given, and any changes made are indicated. See: https://creativecommons.org/licenses/by/4.0/.
spellingShingle Review
Friedlaender, Alex
Addeo, Alfredo
Banna, Giuseppe
New emerging targets in cancer immunotherapy: the role of TIM3
title New emerging targets in cancer immunotherapy: the role of TIM3
title_full New emerging targets in cancer immunotherapy: the role of TIM3
title_fullStr New emerging targets in cancer immunotherapy: the role of TIM3
title_full_unstemmed New emerging targets in cancer immunotherapy: the role of TIM3
title_short New emerging targets in cancer immunotherapy: the role of TIM3
title_sort new emerging targets in cancer immunotherapy: the role of tim3
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6579568/
https://www.ncbi.nlm.nih.gov/pubmed/31275616
http://dx.doi.org/10.1136/esmoopen-2019-000497
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