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Transcutaneous Vagal Nerve Stimulation Alone or in Combination With Radiotherapy Stimulates Lung Tumor Infiltrating Lymphocytes But Fails to Suppress Tumor Growth

The combination of radiotherapy (RT) with immunotherapy represents a promising treatment modality for non-small cell lung cancer (NSCLC) patients. As only a minority of patients shows a persistent response today, a spacious optimization window remains to be explored. Previously we showed that fracti...

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Autores principales: Reijmen, Eva, De Mey, Sven, Van Damme, Helena, De Ridder, Kirsten, Gevaert, Thierry, De Blay, Emmy, Bouwens, Luc, Collen, Christine, Decoster, Lore, De Couck, Marijke, Laoui, Damya, De Grève, Jacques, De Ridder, Mark, Gidron, Yori, Goyvaerts, Cleo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671299/
https://www.ncbi.nlm.nih.gov/pubmed/34925341
http://dx.doi.org/10.3389/fimmu.2021.772555
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author Reijmen, Eva
De Mey, Sven
Van Damme, Helena
De Ridder, Kirsten
Gevaert, Thierry
De Blay, Emmy
Bouwens, Luc
Collen, Christine
Decoster, Lore
De Couck, Marijke
Laoui, Damya
De Grève, Jacques
De Ridder, Mark
Gidron, Yori
Goyvaerts, Cleo
author_facet Reijmen, Eva
De Mey, Sven
Van Damme, Helena
De Ridder, Kirsten
Gevaert, Thierry
De Blay, Emmy
Bouwens, Luc
Collen, Christine
Decoster, Lore
De Couck, Marijke
Laoui, Damya
De Grève, Jacques
De Ridder, Mark
Gidron, Yori
Goyvaerts, Cleo
author_sort Reijmen, Eva
collection PubMed
description The combination of radiotherapy (RT) with immunotherapy represents a promising treatment modality for non-small cell lung cancer (NSCLC) patients. As only a minority of patients shows a persistent response today, a spacious optimization window remains to be explored. Previously we showed that fractionated RT can induce a local immunosuppressive profile. Based on the evolving concept of an immunomodulatory role for vagal nerve stimulation (VNS), we tested its therapeutic and immunological effects alone and in combination with fractionated RT in a preclinical-translational study. Lewis lung carcinoma-bearing C57Bl/6 mice were treated with VNS, fractionated RT or the combination while a patient cohort with locally advanced NSCLC receiving concurrent radiochemotherapy (ccRTCT) was enrolled in a clinical trial to receive either sham or effective VNS daily during their 6 weeks of ccRTCT treatment. Preclinically, VNS alone or with RT showed no therapeutic effect yet VNS alone significantly enhanced the activation profile of intratumoral CD8(+) T cells by upregulating their IFN-γ and CD137 expression. In the periphery, VNS reduced the RT-mediated rise of splenic, but not blood-derived, regulatory T cells (Treg) and monocytes. In accordance, the serological levels of protumoral CXCL5 next to two Treg-attracting chemokines CCL1 and CCL22 were reduced upon VNS monotherapy. In line with our preclinical findings on the lack of immunological changes in blood circulating immune cells upon VNS, immune monitoring of the peripheral blood of VNS treated NSCLC patients (n=7) did not show any significant changes compared to ccRTCT alone. As our preclinical data do suggest that VNS intensifies the stimulatory profile of the tumor infiltrated CD8(+) T cells, this favors further research into non-invasive VNS to optimize current response rates to RT-immunotherapy in lung cancer patients.
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spelling pubmed-86712992021-12-16 Transcutaneous Vagal Nerve Stimulation Alone or in Combination With Radiotherapy Stimulates Lung Tumor Infiltrating Lymphocytes But Fails to Suppress Tumor Growth Reijmen, Eva De Mey, Sven Van Damme, Helena De Ridder, Kirsten Gevaert, Thierry De Blay, Emmy Bouwens, Luc Collen, Christine Decoster, Lore De Couck, Marijke Laoui, Damya De Grève, Jacques De Ridder, Mark Gidron, Yori Goyvaerts, Cleo Front Immunol Immunology The combination of radiotherapy (RT) with immunotherapy represents a promising treatment modality for non-small cell lung cancer (NSCLC) patients. As only a minority of patients shows a persistent response today, a spacious optimization window remains to be explored. Previously we showed that fractionated RT can induce a local immunosuppressive profile. Based on the evolving concept of an immunomodulatory role for vagal nerve stimulation (VNS), we tested its therapeutic and immunological effects alone and in combination with fractionated RT in a preclinical-translational study. Lewis lung carcinoma-bearing C57Bl/6 mice were treated with VNS, fractionated RT or the combination while a patient cohort with locally advanced NSCLC receiving concurrent radiochemotherapy (ccRTCT) was enrolled in a clinical trial to receive either sham or effective VNS daily during their 6 weeks of ccRTCT treatment. Preclinically, VNS alone or with RT showed no therapeutic effect yet VNS alone significantly enhanced the activation profile of intratumoral CD8(+) T cells by upregulating their IFN-γ and CD137 expression. In the periphery, VNS reduced the RT-mediated rise of splenic, but not blood-derived, regulatory T cells (Treg) and monocytes. In accordance, the serological levels of protumoral CXCL5 next to two Treg-attracting chemokines CCL1 and CCL22 were reduced upon VNS monotherapy. In line with our preclinical findings on the lack of immunological changes in blood circulating immune cells upon VNS, immune monitoring of the peripheral blood of VNS treated NSCLC patients (n=7) did not show any significant changes compared to ccRTCT alone. As our preclinical data do suggest that VNS intensifies the stimulatory profile of the tumor infiltrated CD8(+) T cells, this favors further research into non-invasive VNS to optimize current response rates to RT-immunotherapy in lung cancer patients. Frontiers Media S.A. 2021-12-01 /pmc/articles/PMC8671299/ /pubmed/34925341 http://dx.doi.org/10.3389/fimmu.2021.772555 Text en Copyright © 2021 Reijmen, De Mey, Van Damme, De Ridder, Gevaert, De Blay, Bouwens, Collen, Decoster, De Couck, Laoui, De Grève, De Ridder, Gidron and Goyvaerts https://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
Reijmen, Eva
De Mey, Sven
Van Damme, Helena
De Ridder, Kirsten
Gevaert, Thierry
De Blay, Emmy
Bouwens, Luc
Collen, Christine
Decoster, Lore
De Couck, Marijke
Laoui, Damya
De Grève, Jacques
De Ridder, Mark
Gidron, Yori
Goyvaerts, Cleo
Transcutaneous Vagal Nerve Stimulation Alone or in Combination With Radiotherapy Stimulates Lung Tumor Infiltrating Lymphocytes But Fails to Suppress Tumor Growth
title Transcutaneous Vagal Nerve Stimulation Alone or in Combination With Radiotherapy Stimulates Lung Tumor Infiltrating Lymphocytes But Fails to Suppress Tumor Growth
title_full Transcutaneous Vagal Nerve Stimulation Alone or in Combination With Radiotherapy Stimulates Lung Tumor Infiltrating Lymphocytes But Fails to Suppress Tumor Growth
title_fullStr Transcutaneous Vagal Nerve Stimulation Alone or in Combination With Radiotherapy Stimulates Lung Tumor Infiltrating Lymphocytes But Fails to Suppress Tumor Growth
title_full_unstemmed Transcutaneous Vagal Nerve Stimulation Alone or in Combination With Radiotherapy Stimulates Lung Tumor Infiltrating Lymphocytes But Fails to Suppress Tumor Growth
title_short Transcutaneous Vagal Nerve Stimulation Alone or in Combination With Radiotherapy Stimulates Lung Tumor Infiltrating Lymphocytes But Fails to Suppress Tumor Growth
title_sort transcutaneous vagal nerve stimulation alone or in combination with radiotherapy stimulates lung tumor infiltrating lymphocytes but fails to suppress tumor growth
topic Immunology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8671299/
https://www.ncbi.nlm.nih.gov/pubmed/34925341
http://dx.doi.org/10.3389/fimmu.2021.772555
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