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A pilot clinical study of the therapeutic antibody against canine PD-1 for advanced spontaneous cancers in dogs

Inhibition of programmed death 1 (PD-1), expressed on activated T cells, can break through immune resistance and elicit durable responses in human melanoma as well as other types of cancers. Canine oral malignant melanoma is one of the most aggressive tumors bearing poor prognosis due to its high me...

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Autores principales: Igase, Masaya, Nemoto, Yuki, Itamoto, Kazuhito, Tani, Kenji, Nakaichi, Munekazu, Sakurai, Masashi, Sakai, Yusuke, Noguchi, Shunsuke, Kato, Masahiro, Tsukui, Toshihiro, Mizuno, Takuya
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7591904/
https://www.ncbi.nlm.nih.gov/pubmed/33110170
http://dx.doi.org/10.1038/s41598-020-75533-4
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author Igase, Masaya
Nemoto, Yuki
Itamoto, Kazuhito
Tani, Kenji
Nakaichi, Munekazu
Sakurai, Masashi
Sakai, Yusuke
Noguchi, Shunsuke
Kato, Masahiro
Tsukui, Toshihiro
Mizuno, Takuya
author_facet Igase, Masaya
Nemoto, Yuki
Itamoto, Kazuhito
Tani, Kenji
Nakaichi, Munekazu
Sakurai, Masashi
Sakai, Yusuke
Noguchi, Shunsuke
Kato, Masahiro
Tsukui, Toshihiro
Mizuno, Takuya
author_sort Igase, Masaya
collection PubMed
description Inhibition of programmed death 1 (PD-1), expressed on activated T cells, can break through immune resistance and elicit durable responses in human melanoma as well as other types of cancers. Canine oral malignant melanoma is one of the most aggressive tumors bearing poor prognosis due to its high metastatic potency. However, there are few effective treatments for the advanced stages of melanoma in veterinary medicine. Only one previous study indicated the potential of the immune checkpoint inhibitor, anti-canine PD-L1 therapeutic antibody in dogs, and no anti-canine PD-1 therapeutic antibodies are currently available. Here, we developed two therapeutic antibodies, rat-dog chimeric and caninized anti-canine PD-1 monoclonal antibodies and evaluated in vitro functionality for these antibodies. Moreover, we conducted a pilot study to determine their safety profiles and clinical efficacy in spontaneously occurring canine cancers. In conclusion, the anti-canine PD-1 monoclonal antibody was relatively safe and effective in dogs with advanced oral malignant melanoma and other cancers. Thus, our study suggests that PD-1 blockade may be an attractive treatment option in canine cancers.
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spelling pubmed-75919042020-10-28 A pilot clinical study of the therapeutic antibody against canine PD-1 for advanced spontaneous cancers in dogs Igase, Masaya Nemoto, Yuki Itamoto, Kazuhito Tani, Kenji Nakaichi, Munekazu Sakurai, Masashi Sakai, Yusuke Noguchi, Shunsuke Kato, Masahiro Tsukui, Toshihiro Mizuno, Takuya Sci Rep Article Inhibition of programmed death 1 (PD-1), expressed on activated T cells, can break through immune resistance and elicit durable responses in human melanoma as well as other types of cancers. Canine oral malignant melanoma is one of the most aggressive tumors bearing poor prognosis due to its high metastatic potency. However, there are few effective treatments for the advanced stages of melanoma in veterinary medicine. Only one previous study indicated the potential of the immune checkpoint inhibitor, anti-canine PD-L1 therapeutic antibody in dogs, and no anti-canine PD-1 therapeutic antibodies are currently available. Here, we developed two therapeutic antibodies, rat-dog chimeric and caninized anti-canine PD-1 monoclonal antibodies and evaluated in vitro functionality for these antibodies. Moreover, we conducted a pilot study to determine their safety profiles and clinical efficacy in spontaneously occurring canine cancers. In conclusion, the anti-canine PD-1 monoclonal antibody was relatively safe and effective in dogs with advanced oral malignant melanoma and other cancers. Thus, our study suggests that PD-1 blockade may be an attractive treatment option in canine cancers. Nature Publishing Group UK 2020-10-27 /pmc/articles/PMC7591904/ /pubmed/33110170 http://dx.doi.org/10.1038/s41598-020-75533-4 Text en © The Author(s) 2020 Open Access This 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 Article
Igase, Masaya
Nemoto, Yuki
Itamoto, Kazuhito
Tani, Kenji
Nakaichi, Munekazu
Sakurai, Masashi
Sakai, Yusuke
Noguchi, Shunsuke
Kato, Masahiro
Tsukui, Toshihiro
Mizuno, Takuya
A pilot clinical study of the therapeutic antibody against canine PD-1 for advanced spontaneous cancers in dogs
title A pilot clinical study of the therapeutic antibody against canine PD-1 for advanced spontaneous cancers in dogs
title_full A pilot clinical study of the therapeutic antibody against canine PD-1 for advanced spontaneous cancers in dogs
title_fullStr A pilot clinical study of the therapeutic antibody against canine PD-1 for advanced spontaneous cancers in dogs
title_full_unstemmed A pilot clinical study of the therapeutic antibody against canine PD-1 for advanced spontaneous cancers in dogs
title_short A pilot clinical study of the therapeutic antibody against canine PD-1 for advanced spontaneous cancers in dogs
title_sort pilot clinical study of the therapeutic antibody against canine pd-1 for advanced spontaneous cancers in dogs
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7591904/
https://www.ncbi.nlm.nih.gov/pubmed/33110170
http://dx.doi.org/10.1038/s41598-020-75533-4
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