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Immunomodulatory effect of peritumorally administered interferon-beta on melanoma through tumor-associated macrophages

An imbalance of immunosuppressive cells and cytotoxic cells plays an important role in the tumor-bearing host. Together with regulatory T cells (Tregs), tumor-associated macrophages (TAMs) play roles in maintaining the tumor microenvironment. Since interferon beta (IFN-β) has been clinically used fo...

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Autores principales: Kakizaki, Aya, Fujimura, Taku, Furudate, Sadanori, Kambayashi, Yumi, Yamauchi, Takeshi, Yagita, Hideo, Aiba, Setsuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Taylor & Francis 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4589056/
https://www.ncbi.nlm.nih.gov/pubmed/26451326
http://dx.doi.org/10.1080/2162402X.2015.1047584
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author Kakizaki, Aya
Fujimura, Taku
Furudate, Sadanori
Kambayashi, Yumi
Yamauchi, Takeshi
Yagita, Hideo
Aiba, Setsuya
author_facet Kakizaki, Aya
Fujimura, Taku
Furudate, Sadanori
Kambayashi, Yumi
Yamauchi, Takeshi
Yagita, Hideo
Aiba, Setsuya
author_sort Kakizaki, Aya
collection PubMed
description An imbalance of immunosuppressive cells and cytotoxic cells plays an important role in the tumor-bearing host. Together with regulatory T cells (Tregs), tumor-associated macrophages (TAMs) play roles in maintaining the tumor microenvironment. Since interferon beta (IFN-β) has been clinically used for the treatment of malignant melanoma, we investigated the immunomodulatory effect of IFN-β during melanoma growth to elucidate the effects of IFN-β on the tumor microenvironment by using the B16F10 melanoma model. Peritumorally administered IFN-β significantly decreased the mRNA expression and production of Th2-related chemokines, which suppressed the recruitment of Tregs in B16F10 melanoma. Since the administration of IFN-β augments the expression of PD-1 on TILs, the co-administration of anti-PD-1 Ab augmented the therapeutic effect of IFN-β for the treatment of B16F10 melanoma. Moreover, in parallel with the mouse model, in the human system, IFN-β decreased the production of Th2-related chemokines and augmented the production of Th1-related chemokines from monocyte-derived M2 macrophages. Since these immunomodulatory effects of IFN-β on macrophages were also observed in the lesional skin of human in-transit melanoma, our present data suggest one of the possible immunomodulatory effects of IFN-β and support the possibility of IFN-β in combination with anti-PD-1 Ab for the treatment of melanoma.
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spelling pubmed-45890562016-02-03 Immunomodulatory effect of peritumorally administered interferon-beta on melanoma through tumor-associated macrophages Kakizaki, Aya Fujimura, Taku Furudate, Sadanori Kambayashi, Yumi Yamauchi, Takeshi Yagita, Hideo Aiba, Setsuya Oncoimmunology Original Research An imbalance of immunosuppressive cells and cytotoxic cells plays an important role in the tumor-bearing host. Together with regulatory T cells (Tregs), tumor-associated macrophages (TAMs) play roles in maintaining the tumor microenvironment. Since interferon beta (IFN-β) has been clinically used for the treatment of malignant melanoma, we investigated the immunomodulatory effect of IFN-β during melanoma growth to elucidate the effects of IFN-β on the tumor microenvironment by using the B16F10 melanoma model. Peritumorally administered IFN-β significantly decreased the mRNA expression and production of Th2-related chemokines, which suppressed the recruitment of Tregs in B16F10 melanoma. Since the administration of IFN-β augments the expression of PD-1 on TILs, the co-administration of anti-PD-1 Ab augmented the therapeutic effect of IFN-β for the treatment of B16F10 melanoma. Moreover, in parallel with the mouse model, in the human system, IFN-β decreased the production of Th2-related chemokines and augmented the production of Th1-related chemokines from monocyte-derived M2 macrophages. Since these immunomodulatory effects of IFN-β on macrophages were also observed in the lesional skin of human in-transit melanoma, our present data suggest one of the possible immunomodulatory effects of IFN-β and support the possibility of IFN-β in combination with anti-PD-1 Ab for the treatment of melanoma. Taylor & Francis 2015-05-26 /pmc/articles/PMC4589056/ /pubmed/26451326 http://dx.doi.org/10.1080/2162402X.2015.1047584 Text en © 2015 The Author(s). Published with license by Taylor & Francis Group, LLC http://creativecommons.org/licenses/by-nc/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Non-Commercial License http://creativecommons.org/licenses/by-nc/3.0/, which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. The moral rights of the named author(s) have been asserted.
spellingShingle Original Research
Kakizaki, Aya
Fujimura, Taku
Furudate, Sadanori
Kambayashi, Yumi
Yamauchi, Takeshi
Yagita, Hideo
Aiba, Setsuya
Immunomodulatory effect of peritumorally administered interferon-beta on melanoma through tumor-associated macrophages
title Immunomodulatory effect of peritumorally administered interferon-beta on melanoma through tumor-associated macrophages
title_full Immunomodulatory effect of peritumorally administered interferon-beta on melanoma through tumor-associated macrophages
title_fullStr Immunomodulatory effect of peritumorally administered interferon-beta on melanoma through tumor-associated macrophages
title_full_unstemmed Immunomodulatory effect of peritumorally administered interferon-beta on melanoma through tumor-associated macrophages
title_short Immunomodulatory effect of peritumorally administered interferon-beta on melanoma through tumor-associated macrophages
title_sort immunomodulatory effect of peritumorally administered interferon-beta on melanoma through tumor-associated macrophages
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4589056/
https://www.ncbi.nlm.nih.gov/pubmed/26451326
http://dx.doi.org/10.1080/2162402X.2015.1047584
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