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New emerging targets in cancer immunotherapy: CD27 (TNFRSF7)
Cluster of differentiation 27 (CD27) is a member of the tumour necrosis factor receptor superfamily and plays a key role in T-cell activation by providing a costimulatory signal. Bound to its natural ligand CD70, CD27 signalling enhances T-cell proliferation and differentiation to effector and memor...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BMJ Publishing Group
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082637/ https://www.ncbi.nlm.nih.gov/pubmed/32152062 http://dx.doi.org/10.1136/esmoopen-2019-000629 |
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author | Starzer, Angelika M. Berghoff, Anna S. |
author_facet | Starzer, Angelika M. Berghoff, Anna S. |
author_sort | Starzer, Angelika M. |
collection | PubMed |
description | Cluster of differentiation 27 (CD27) is a member of the tumour necrosis factor receptor superfamily and plays a key role in T-cell activation by providing a costimulatory signal. Bound to its natural ligand CD70, CD27 signalling enhances T-cell proliferation and differentiation to effector and memory T cells and therefore has potential as an immune modulatory target in cancer treatment. The CD27 agonistic antibody varlilumab showed promising efficacy in haematological as well as solid cancers. Current studies investigate the combination of the CD27 agonistic antibody varlilumab in combination with the PD1 axis targeting immune checkpoint inhibitors like nivolumab or atezolizumab. Further, CD70 expression is used as a therapeutic target for ADCs, antibodies inducing ADCC, as well as the immunological target for chimeric antigen receptor gene-modified T cells and specific dendritic cell vaccination. In line with this, targeting the CD27 axis was shown to be feasible and safe in early clinical trials with the most commonly occurring side effects being thrombocytopenia, fatigue and nausea. In this mini review, we aimed to elucidate the immunobiology of CD27 and its potential as a target in cancer immunotherapy. |
format | Online Article Text |
id | pubmed-7082637 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BMJ Publishing Group |
record_format | MEDLINE/PubMed |
spelling | pubmed-70826372020-03-23 New emerging targets in cancer immunotherapy: CD27 (TNFRSF7) Starzer, Angelika M. Berghoff, Anna S. ESMO Open Review Cluster of differentiation 27 (CD27) is a member of the tumour necrosis factor receptor superfamily and plays a key role in T-cell activation by providing a costimulatory signal. Bound to its natural ligand CD70, CD27 signalling enhances T-cell proliferation and differentiation to effector and memory T cells and therefore has potential as an immune modulatory target in cancer treatment. The CD27 agonistic antibody varlilumab showed promising efficacy in haematological as well as solid cancers. Current studies investigate the combination of the CD27 agonistic antibody varlilumab in combination with the PD1 axis targeting immune checkpoint inhibitors like nivolumab or atezolizumab. Further, CD70 expression is used as a therapeutic target for ADCs, antibodies inducing ADCC, as well as the immunological target for chimeric antigen receptor gene-modified T cells and specific dendritic cell vaccination. In line with this, targeting the CD27 axis was shown to be feasible and safe in early clinical trials with the most commonly occurring side effects being thrombocytopenia, fatigue and nausea. In this mini review, we aimed to elucidate the immunobiology of CD27 and its potential as a target in cancer immunotherapy. BMJ Publishing Group 2020-03-09 /pmc/articles/PMC7082637/ /pubmed/32152062 http://dx.doi.org/10.1136/esmoopen-2019-000629 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 Starzer, Angelika M. Berghoff, Anna S. New emerging targets in cancer immunotherapy: CD27 (TNFRSF7) |
title | New emerging targets in cancer immunotherapy: CD27 (TNFRSF7) |
title_full | New emerging targets in cancer immunotherapy: CD27 (TNFRSF7) |
title_fullStr | New emerging targets in cancer immunotherapy: CD27 (TNFRSF7) |
title_full_unstemmed | New emerging targets in cancer immunotherapy: CD27 (TNFRSF7) |
title_short | New emerging targets in cancer immunotherapy: CD27 (TNFRSF7) |
title_sort | new emerging targets in cancer immunotherapy: cd27 (tnfrsf7) |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7082637/ https://www.ncbi.nlm.nih.gov/pubmed/32152062 http://dx.doi.org/10.1136/esmoopen-2019-000629 |
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