Cargando…
New emerging targets in cancer immunotherapy: CD137/4-1BB costimulatory axis
CD137 (4-1BB) is a surface glycoprotein that belongs to the tumour necrosis factor receptor family (TNFRSF9). Its expression is induced on activation on a number of leucocyte types. Interestingly, for cancer immunotherapy, CD137 becomes expressed on primed T and natural killer (NK) cells, which on l...
Autores principales: | , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333812/ https://www.ncbi.nlm.nih.gov/pubmed/32611557 http://dx.doi.org/10.1136/esmoopen-2020-000733 |
_version_ | 1783553823941328896 |
---|---|
author | Etxeberria, Iñaki Glez-Vaz, Javier Teijeira, Álvaro Melero, Ignacio |
author_facet | Etxeberria, Iñaki Glez-Vaz, Javier Teijeira, Álvaro Melero, Ignacio |
author_sort | Etxeberria, Iñaki |
collection | PubMed |
description | CD137 (4-1BB) is a surface glycoprotein that belongs to the tumour necrosis factor receptor family (TNFRSF9). Its expression is induced on activation on a number of leucocyte types. Interestingly, for cancer immunotherapy, CD137 becomes expressed on primed T and natural killer (NK) cells, which on ligation provides powerful costimulatory signals. Perturbation of CD137 by CD137L or agonist monoclonal antibodies on activated CD8 T cells protects such antigen-specific cytotoxic T lymphocytes from apoptosis, enhances effector functionalities and favours persistence and memory differentiation. As a consequence, agonist antibodies exert potent antitumour effects in mouse models and the CD137 signalling domain is critical in chimeric antigen receptors (CAR) of CAR T cells approved to be used in the clinic. New formats of CD137 agonist moieties are being clinically developed, seeking potent costimulation targeted to the tumour microenvironment to avoid liver inflammation side effects, that have thus far limited and delayed clinical development. |
format | Online Article Text |
id | pubmed-7333812 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-73338122020-07-07 New emerging targets in cancer immunotherapy: CD137/4-1BB costimulatory axis Etxeberria, Iñaki Glez-Vaz, Javier Teijeira, Álvaro Melero, Ignacio ESMO Open Review CD137 (4-1BB) is a surface glycoprotein that belongs to the tumour necrosis factor receptor family (TNFRSF9). Its expression is induced on activation on a number of leucocyte types. Interestingly, for cancer immunotherapy, CD137 becomes expressed on primed T and natural killer (NK) cells, which on ligation provides powerful costimulatory signals. Perturbation of CD137 by CD137L or agonist monoclonal antibodies on activated CD8 T cells protects such antigen-specific cytotoxic T lymphocytes from apoptosis, enhances effector functionalities and favours persistence and memory differentiation. As a consequence, agonist antibodies exert potent antitumour effects in mouse models and the CD137 signalling domain is critical in chimeric antigen receptors (CAR) of CAR T cells approved to be used in the clinic. New formats of CD137 agonist moieties are being clinically developed, seeking potent costimulation targeted to the tumour microenvironment to avoid liver inflammation side effects, that have thus far limited and delayed clinical development. BMJ Publishing Group 2020-07-01 /pmc/articles/PMC7333812/ /pubmed/32611557 http://dx.doi.org/10.1136/esmoopen-2020-000733 Text en © Author (s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. Published by BMJ on behalf of the European Society for Medical Oncology. http://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, any changes made are indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/. |
spellingShingle | Review Etxeberria, Iñaki Glez-Vaz, Javier Teijeira, Álvaro Melero, Ignacio New emerging targets in cancer immunotherapy: CD137/4-1BB costimulatory axis |
title | New emerging targets in cancer immunotherapy: CD137/4-1BB costimulatory axis |
title_full | New emerging targets in cancer immunotherapy: CD137/4-1BB costimulatory axis |
title_fullStr | New emerging targets in cancer immunotherapy: CD137/4-1BB costimulatory axis |
title_full_unstemmed | New emerging targets in cancer immunotherapy: CD137/4-1BB costimulatory axis |
title_short | New emerging targets in cancer immunotherapy: CD137/4-1BB costimulatory axis |
title_sort | new emerging targets in cancer immunotherapy: cd137/4-1bb costimulatory axis |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7333812/ https://www.ncbi.nlm.nih.gov/pubmed/32611557 http://dx.doi.org/10.1136/esmoopen-2020-000733 |
work_keys_str_mv | AT etxeberriainaki newemergingtargetsincancerimmunotherapycd13741bbcostimulatoryaxis AT glezvazjavier newemergingtargetsincancerimmunotherapycd13741bbcostimulatoryaxis AT teijeiraalvaro newemergingtargetsincancerimmunotherapycd13741bbcostimulatoryaxis AT meleroignacio newemergingtargetsincancerimmunotherapycd13741bbcostimulatoryaxis |