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In vitro assessment of antitumor immune responses using tumor antigen proteins produced by transgenic silkworms
The evaluation of antitumor immune responses is essential for immune monitoring to predict clinical outcomes as well as treatment efficacies in cancer patients. In this study, we produced two tumor antigen (TA) proteins, melanoma antigen family A4 and wild type p53, using TG silkworm systems and eva...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer US
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128804/ https://www.ncbi.nlm.nih.gov/pubmed/33999320 http://dx.doi.org/10.1007/s10856-021-06526-6 |
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author | Yamada, Kanae Masuda, Kei Ida, Shota Tada, Hiroe Bando, Minori Abe, Kanako Tatematsu, Ken-ichiro Sezutsu, Hideki Oyama, Tetsunari Chikamatsu, Kazuaki Takeda, Shigeki |
author_facet | Yamada, Kanae Masuda, Kei Ida, Shota Tada, Hiroe Bando, Minori Abe, Kanako Tatematsu, Ken-ichiro Sezutsu, Hideki Oyama, Tetsunari Chikamatsu, Kazuaki Takeda, Shigeki |
author_sort | Yamada, Kanae |
collection | PubMed |
description | The evaluation of antitumor immune responses is essential for immune monitoring to predict clinical outcomes as well as treatment efficacies in cancer patients. In this study, we produced two tumor antigen (TA) proteins, melanoma antigen family A4 and wild type p53, using TG silkworm systems and evaluated anti-TA-specific immune responses by enzyme-linked immunosorbent spot assays in patients with head and neck cancer. Eleven (61.1%) of 18 patients showed significant IFN-γ production in response to at least one TA; however, the presence of TA-specific immune responses did not significantly contribute to better prognosis (overall survival, p = 0.1768; progression-free survival, p = 0.4507). Further studies will need to be performed on a larger scale to better assess the clinical significance of these systems. The production of multiple TA proteins may provide new avenues for the development of immunotherapeutic strategies to stimulate a potent and specific immune response against tumor cells as well as precise assessment of antitumor immune responses in cancer patients. [Image: see text] |
format | Online Article Text |
id | pubmed-8128804 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | Springer US |
record_format | MEDLINE/PubMed |
spelling | pubmed-81288042021-05-24 In vitro assessment of antitumor immune responses using tumor antigen proteins produced by transgenic silkworms Yamada, Kanae Masuda, Kei Ida, Shota Tada, Hiroe Bando, Minori Abe, Kanako Tatematsu, Ken-ichiro Sezutsu, Hideki Oyama, Tetsunari Chikamatsu, Kazuaki Takeda, Shigeki J Mater Sci Mater Med Biocompatibility Studies The evaluation of antitumor immune responses is essential for immune monitoring to predict clinical outcomes as well as treatment efficacies in cancer patients. In this study, we produced two tumor antigen (TA) proteins, melanoma antigen family A4 and wild type p53, using TG silkworm systems and evaluated anti-TA-specific immune responses by enzyme-linked immunosorbent spot assays in patients with head and neck cancer. Eleven (61.1%) of 18 patients showed significant IFN-γ production in response to at least one TA; however, the presence of TA-specific immune responses did not significantly contribute to better prognosis (overall survival, p = 0.1768; progression-free survival, p = 0.4507). Further studies will need to be performed on a larger scale to better assess the clinical significance of these systems. The production of multiple TA proteins may provide new avenues for the development of immunotherapeutic strategies to stimulate a potent and specific immune response against tumor cells as well as precise assessment of antitumor immune responses in cancer patients. [Image: see text] Springer US 2021-05-17 2021 /pmc/articles/PMC8128804/ /pubmed/33999320 http://dx.doi.org/10.1007/s10856-021-06526-6 Text en © The Author(s) 2021 https://creativecommons.org/licenses/by/4.0/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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Biocompatibility Studies Yamada, Kanae Masuda, Kei Ida, Shota Tada, Hiroe Bando, Minori Abe, Kanako Tatematsu, Ken-ichiro Sezutsu, Hideki Oyama, Tetsunari Chikamatsu, Kazuaki Takeda, Shigeki In vitro assessment of antitumor immune responses using tumor antigen proteins produced by transgenic silkworms |
title | In vitro assessment of antitumor immune responses using tumor antigen proteins produced by transgenic silkworms |
title_full | In vitro assessment of antitumor immune responses using tumor antigen proteins produced by transgenic silkworms |
title_fullStr | In vitro assessment of antitumor immune responses using tumor antigen proteins produced by transgenic silkworms |
title_full_unstemmed | In vitro assessment of antitumor immune responses using tumor antigen proteins produced by transgenic silkworms |
title_short | In vitro assessment of antitumor immune responses using tumor antigen proteins produced by transgenic silkworms |
title_sort | in vitro assessment of antitumor immune responses using tumor antigen proteins produced by transgenic silkworms |
topic | Biocompatibility Studies |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8128804/ https://www.ncbi.nlm.nih.gov/pubmed/33999320 http://dx.doi.org/10.1007/s10856-021-06526-6 |
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