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TNFSF14: LIGHTing the Way for Effective Cancer Immunotherapy
Tumor necrosis factor superfamily member 14 (LIGHT) has been in pre-clinical development for over a decade and shows promise as a modality of enhancing treatment approaches in the field of cancer immunotherapy. To date, LIGHT has been used to combat cancer in multiple tumor models where it can be co...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Frontiers Media S.A.
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7243824/ https://www.ncbi.nlm.nih.gov/pubmed/32499782 http://dx.doi.org/10.3389/fimmu.2020.00922 |
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author | Skeate, Joseph G. Otsmaa, Mikk E. Prins, Ruben Fernandez, Daniel J. Da Silva, Diane M. Kast, W. Martin |
author_facet | Skeate, Joseph G. Otsmaa, Mikk E. Prins, Ruben Fernandez, Daniel J. Da Silva, Diane M. Kast, W. Martin |
author_sort | Skeate, Joseph G. |
collection | PubMed |
description | Tumor necrosis factor superfamily member 14 (LIGHT) has been in pre-clinical development for over a decade and shows promise as a modality of enhancing treatment approaches in the field of cancer immunotherapy. To date, LIGHT has been used to combat cancer in multiple tumor models where it can be combined with other immunotherapy modalities to clear established solid tumors as well as treat metastatic events. When LIGHT molecules are delivered to or expressed within tumors they cause significant changes in the tumor microenvironment that are primarily driven through vascular normalization and generation of tertiary lymphoid structures. These changes can synergize with methods that induce or support anti-tumor immune responses, such as checkpoint inhibitors and/or tumor vaccines, to greatly improve immunotherapeutic strategies against cancer. While investigators have utilized multiple vectors to LIGHT-up tumor tissues, there are still improvements needed and components to be found within a human tumor microenvironment that may impede translational efforts. This review addresses the current state of this field. |
format | Online Article Text |
id | pubmed-7243824 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Frontiers Media S.A. |
record_format | MEDLINE/PubMed |
spelling | pubmed-72438242020-06-03 TNFSF14: LIGHTing the Way for Effective Cancer Immunotherapy Skeate, Joseph G. Otsmaa, Mikk E. Prins, Ruben Fernandez, Daniel J. Da Silva, Diane M. Kast, W. Martin Front Immunol Immunology Tumor necrosis factor superfamily member 14 (LIGHT) has been in pre-clinical development for over a decade and shows promise as a modality of enhancing treatment approaches in the field of cancer immunotherapy. To date, LIGHT has been used to combat cancer in multiple tumor models where it can be combined with other immunotherapy modalities to clear established solid tumors as well as treat metastatic events. When LIGHT molecules are delivered to or expressed within tumors they cause significant changes in the tumor microenvironment that are primarily driven through vascular normalization and generation of tertiary lymphoid structures. These changes can synergize with methods that induce or support anti-tumor immune responses, such as checkpoint inhibitors and/or tumor vaccines, to greatly improve immunotherapeutic strategies against cancer. While investigators have utilized multiple vectors to LIGHT-up tumor tissues, there are still improvements needed and components to be found within a human tumor microenvironment that may impede translational efforts. This review addresses the current state of this field. Frontiers Media S.A. 2020-05-15 /pmc/articles/PMC7243824/ /pubmed/32499782 http://dx.doi.org/10.3389/fimmu.2020.00922 Text en Copyright © 2020 Skeate, Otsmaa, Prins, Fernandez, Da Silva and Kast. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
spellingShingle | Immunology Skeate, Joseph G. Otsmaa, Mikk E. Prins, Ruben Fernandez, Daniel J. Da Silva, Diane M. Kast, W. Martin TNFSF14: LIGHTing the Way for Effective Cancer Immunotherapy |
title | TNFSF14: LIGHTing the Way for Effective Cancer Immunotherapy |
title_full | TNFSF14: LIGHTing the Way for Effective Cancer Immunotherapy |
title_fullStr | TNFSF14: LIGHTing the Way for Effective Cancer Immunotherapy |
title_full_unstemmed | TNFSF14: LIGHTing the Way for Effective Cancer Immunotherapy |
title_short | TNFSF14: LIGHTing the Way for Effective Cancer Immunotherapy |
title_sort | tnfsf14: lighting the way for effective cancer immunotherapy |
topic | Immunology |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7243824/ https://www.ncbi.nlm.nih.gov/pubmed/32499782 http://dx.doi.org/10.3389/fimmu.2020.00922 |
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