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Fingolimod and tumor-infiltrating lymphocytes in checkpoint-inhibitor treated cancer patients
Immune checkpoint inhibitors (ICIs) are emerging as the new standard of care for treating various metastatic cancers. It is known that effective anti-tumor immune responses are associated with a stronger presence of tumor-infiltrating lymphocytes (TILs) in solid tumor tissue. Cancer patients with re...
Autores principales: | , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889549/ https://www.ncbi.nlm.nih.gov/pubmed/32804246 http://dx.doi.org/10.1007/s00262-020-02693-7 |
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author | Hasan Ali, Omar Berner, Fiamma Ackermann, Christoph Jakob Ring, Sandra Stephanie Moulin, Alexandre Müller, Joachim Markert, Eva Pop, Oltin Tiberiu Müller, Stefanie Diem, Stefan Hundsberger, Thomas Flatz, Lukas |
author_facet | Hasan Ali, Omar Berner, Fiamma Ackermann, Christoph Jakob Ring, Sandra Stephanie Moulin, Alexandre Müller, Joachim Markert, Eva Pop, Oltin Tiberiu Müller, Stefanie Diem, Stefan Hundsberger, Thomas Flatz, Lukas |
author_sort | Hasan Ali, Omar |
collection | PubMed |
description | Immune checkpoint inhibitors (ICIs) are emerging as the new standard of care for treating various metastatic cancers. It is known that effective anti-tumor immune responses are associated with a stronger presence of tumor-infiltrating lymphocytes (TILs) in solid tumor tissue. Cancer patients with relapsing–remitting multiple sclerosis (RRMS) are often under continuous treatment with fingolimod, an immune-modulating drug that inhibits lymphocyte egress from secondary lymphatic organs. Little is known about the effect of fingolimod on ICI cancer therapy, as fingolimod may limit the number of TILs. Here we present three patients with RRMS, who developed various cancers during fingolimod treatment. Histology of all tumors consistently showed low numbers of TILs. A second biopsy taken from one of the tumors, a melanoma, revealed a significant increase of TILs after stopping fingolimod and starting pembrolizumab, indicating a surge in the number and re-invigoration of T cells. Our study suggests that fingolimod limits the number of TILs in solid tumors and may, thus, inhibit anti-cancer immune responses. |
format | Online Article Text |
id | pubmed-7889549 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-78895492021-03-03 Fingolimod and tumor-infiltrating lymphocytes in checkpoint-inhibitor treated cancer patients Hasan Ali, Omar Berner, Fiamma Ackermann, Christoph Jakob Ring, Sandra Stephanie Moulin, Alexandre Müller, Joachim Markert, Eva Pop, Oltin Tiberiu Müller, Stefanie Diem, Stefan Hundsberger, Thomas Flatz, Lukas Cancer Immunol Immunother Research Report Immune checkpoint inhibitors (ICIs) are emerging as the new standard of care for treating various metastatic cancers. It is known that effective anti-tumor immune responses are associated with a stronger presence of tumor-infiltrating lymphocytes (TILs) in solid tumor tissue. Cancer patients with relapsing–remitting multiple sclerosis (RRMS) are often under continuous treatment with fingolimod, an immune-modulating drug that inhibits lymphocyte egress from secondary lymphatic organs. Little is known about the effect of fingolimod on ICI cancer therapy, as fingolimod may limit the number of TILs. Here we present three patients with RRMS, who developed various cancers during fingolimod treatment. Histology of all tumors consistently showed low numbers of TILs. A second biopsy taken from one of the tumors, a melanoma, revealed a significant increase of TILs after stopping fingolimod and starting pembrolizumab, indicating a surge in the number and re-invigoration of T cells. Our study suggests that fingolimod limits the number of TILs in solid tumors and may, thus, inhibit anti-cancer immune responses. Springer Berlin Heidelberg 2020-08-17 2021 /pmc/articles/PMC7889549/ /pubmed/32804246 http://dx.doi.org/10.1007/s00262-020-02693-7 Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Research Report Hasan Ali, Omar Berner, Fiamma Ackermann, Christoph Jakob Ring, Sandra Stephanie Moulin, Alexandre Müller, Joachim Markert, Eva Pop, Oltin Tiberiu Müller, Stefanie Diem, Stefan Hundsberger, Thomas Flatz, Lukas Fingolimod and tumor-infiltrating lymphocytes in checkpoint-inhibitor treated cancer patients |
title | Fingolimod and tumor-infiltrating lymphocytes in checkpoint-inhibitor treated cancer patients |
title_full | Fingolimod and tumor-infiltrating lymphocytes in checkpoint-inhibitor treated cancer patients |
title_fullStr | Fingolimod and tumor-infiltrating lymphocytes in checkpoint-inhibitor treated cancer patients |
title_full_unstemmed | Fingolimod and tumor-infiltrating lymphocytes in checkpoint-inhibitor treated cancer patients |
title_short | Fingolimod and tumor-infiltrating lymphocytes in checkpoint-inhibitor treated cancer patients |
title_sort | fingolimod and tumor-infiltrating lymphocytes in checkpoint-inhibitor treated cancer patients |
topic | Research Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7889549/ https://www.ncbi.nlm.nih.gov/pubmed/32804246 http://dx.doi.org/10.1007/s00262-020-02693-7 |
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