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Fractionated Radiotherapy with 3 x 8 Gy Induces Systemic Anti-Tumour Responses and Abscopal Tumour Inhibition without Modulating the Humoral Anti-Tumour Response

Accumulating evidence indicates that fractionated radiotherapy (RT) can result in distant non-irradiated (abscopal) tumour regression. Although preclinical studies indicate the importance of T cells in this infrequent phenomenon, these studies do not preclude that other immune mechanisms exhibit an...

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Autores principales: Habets, Thomas H. P. M., Oth, Tammy, Houben, Ans W., Huijskens, Mirelle J. A. J., Senden-Gijsbers, Birgit L. M. G., Schnijderberg, Melanie C. A., Brans, Boudewijn, Dubois, Ludwig J., Lambin, Philippe, De Saint-Hubert, Marijke, Germeraad, Wilfred T. V., Tilanus, Marcel G. J., Mottaghy, Felix M., Bos, Gerard M. J., Vanderlocht, Joris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948777/
https://www.ncbi.nlm.nih.gov/pubmed/27427766
http://dx.doi.org/10.1371/journal.pone.0159515
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author Habets, Thomas H. P. M.
Oth, Tammy
Houben, Ans W.
Huijskens, Mirelle J. A. J.
Senden-Gijsbers, Birgit L. M. G.
Schnijderberg, Melanie C. A.
Brans, Boudewijn
Dubois, Ludwig J.
Lambin, Philippe
De Saint-Hubert, Marijke
Germeraad, Wilfred T. V.
Tilanus, Marcel G. J.
Mottaghy, Felix M.
Bos, Gerard M. J.
Vanderlocht, Joris
author_facet Habets, Thomas H. P. M.
Oth, Tammy
Houben, Ans W.
Huijskens, Mirelle J. A. J.
Senden-Gijsbers, Birgit L. M. G.
Schnijderberg, Melanie C. A.
Brans, Boudewijn
Dubois, Ludwig J.
Lambin, Philippe
De Saint-Hubert, Marijke
Germeraad, Wilfred T. V.
Tilanus, Marcel G. J.
Mottaghy, Felix M.
Bos, Gerard M. J.
Vanderlocht, Joris
author_sort Habets, Thomas H. P. M.
collection PubMed
description Accumulating evidence indicates that fractionated radiotherapy (RT) can result in distant non-irradiated (abscopal) tumour regression. Although preclinical studies indicate the importance of T cells in this infrequent phenomenon, these studies do not preclude that other immune mechanisms exhibit an addition role in the abscopal effect. We therefore addressed the question whether in addition to T cell mediated responses also humoral anti-tumour responses are modulated after fractionated RT and whether systemic dendritic cell (DC) stimulation can enhance tumour-specific antibody production. We selected the 67NR mammary carcinoma model since this tumour showed spontaneous antibody production in all tumour-bearing mice. Fractionated RT to the primary tumour was associated with a survival benefit and a delayed growth of a non-irradiated (contralateral) secondary tumour. Notably, fractionated RT did not affect anti-tumour antibody titers and the composition of the immunoglobulin (Ig) isotypes. Likewise, we demonstrated that treatment of tumour-bearing Balb/C mice with DC stimulating growth factor Flt3-L did neither modulate the magnitude nor the composition of the humoral immune response. Finally, we evaluated the immune infiltrate and Ig isotype content of the tumour tissue using flow cytometry and found no differences between treatment groups that were indicative for local antibody production. In conclusion, we demonstrate that the 67NR mammary carcinoma in Balb/C mice is associated with a pre-existing antibody response. And, we show that in tumour-bearing Balb/C mice with abscopal tumour regression such pre-existing antibody responses are not altered upon fractionated RT and/or DC stimulation with Flt3-L. Our research indicates that evaluating the humoral immune response in the setting of abscopal tumour regression is not invariably associated with therapeutic effects.
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spelling pubmed-49487772016-08-01 Fractionated Radiotherapy with 3 x 8 Gy Induces Systemic Anti-Tumour Responses and Abscopal Tumour Inhibition without Modulating the Humoral Anti-Tumour Response Habets, Thomas H. P. M. Oth, Tammy Houben, Ans W. Huijskens, Mirelle J. A. J. Senden-Gijsbers, Birgit L. M. G. Schnijderberg, Melanie C. A. Brans, Boudewijn Dubois, Ludwig J. Lambin, Philippe De Saint-Hubert, Marijke Germeraad, Wilfred T. V. Tilanus, Marcel G. J. Mottaghy, Felix M. Bos, Gerard M. J. Vanderlocht, Joris PLoS One Research Article Accumulating evidence indicates that fractionated radiotherapy (RT) can result in distant non-irradiated (abscopal) tumour regression. Although preclinical studies indicate the importance of T cells in this infrequent phenomenon, these studies do not preclude that other immune mechanisms exhibit an addition role in the abscopal effect. We therefore addressed the question whether in addition to T cell mediated responses also humoral anti-tumour responses are modulated after fractionated RT and whether systemic dendritic cell (DC) stimulation can enhance tumour-specific antibody production. We selected the 67NR mammary carcinoma model since this tumour showed spontaneous antibody production in all tumour-bearing mice. Fractionated RT to the primary tumour was associated with a survival benefit and a delayed growth of a non-irradiated (contralateral) secondary tumour. Notably, fractionated RT did not affect anti-tumour antibody titers and the composition of the immunoglobulin (Ig) isotypes. Likewise, we demonstrated that treatment of tumour-bearing Balb/C mice with DC stimulating growth factor Flt3-L did neither modulate the magnitude nor the composition of the humoral immune response. Finally, we evaluated the immune infiltrate and Ig isotype content of the tumour tissue using flow cytometry and found no differences between treatment groups that were indicative for local antibody production. In conclusion, we demonstrate that the 67NR mammary carcinoma in Balb/C mice is associated with a pre-existing antibody response. And, we show that in tumour-bearing Balb/C mice with abscopal tumour regression such pre-existing antibody responses are not altered upon fractionated RT and/or DC stimulation with Flt3-L. Our research indicates that evaluating the humoral immune response in the setting of abscopal tumour regression is not invariably associated with therapeutic effects. Public Library of Science 2016-07-18 /pmc/articles/PMC4948777/ /pubmed/27427766 http://dx.doi.org/10.1371/journal.pone.0159515 Text en © 2016 Habets et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Habets, Thomas H. P. M.
Oth, Tammy
Houben, Ans W.
Huijskens, Mirelle J. A. J.
Senden-Gijsbers, Birgit L. M. G.
Schnijderberg, Melanie C. A.
Brans, Boudewijn
Dubois, Ludwig J.
Lambin, Philippe
De Saint-Hubert, Marijke
Germeraad, Wilfred T. V.
Tilanus, Marcel G. J.
Mottaghy, Felix M.
Bos, Gerard M. J.
Vanderlocht, Joris
Fractionated Radiotherapy with 3 x 8 Gy Induces Systemic Anti-Tumour Responses and Abscopal Tumour Inhibition without Modulating the Humoral Anti-Tumour Response
title Fractionated Radiotherapy with 3 x 8 Gy Induces Systemic Anti-Tumour Responses and Abscopal Tumour Inhibition without Modulating the Humoral Anti-Tumour Response
title_full Fractionated Radiotherapy with 3 x 8 Gy Induces Systemic Anti-Tumour Responses and Abscopal Tumour Inhibition without Modulating the Humoral Anti-Tumour Response
title_fullStr Fractionated Radiotherapy with 3 x 8 Gy Induces Systemic Anti-Tumour Responses and Abscopal Tumour Inhibition without Modulating the Humoral Anti-Tumour Response
title_full_unstemmed Fractionated Radiotherapy with 3 x 8 Gy Induces Systemic Anti-Tumour Responses and Abscopal Tumour Inhibition without Modulating the Humoral Anti-Tumour Response
title_short Fractionated Radiotherapy with 3 x 8 Gy Induces Systemic Anti-Tumour Responses and Abscopal Tumour Inhibition without Modulating the Humoral Anti-Tumour Response
title_sort fractionated radiotherapy with 3 x 8 gy induces systemic anti-tumour responses and abscopal tumour inhibition without modulating the humoral anti-tumour response
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4948777/
https://www.ncbi.nlm.nih.gov/pubmed/27427766
http://dx.doi.org/10.1371/journal.pone.0159515
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