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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2020
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.
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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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