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Japanese Kampo Medicine Juzentaihoto Enhances Antitumor Immunity in CD1d(−/−) Mice Lacking NKT Cells
Although the Japanese traditional herbal medicine (Kampo), Juzentaihoto (JTT), has been reported to have antitumor effects in several tumor models, its role in tumor immunology remains controversial. In the present study, we tested whether oral administration of JTT enhances antitumor immunity in CD...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
SAGE Publications
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6974754/ https://www.ncbi.nlm.nih.gov/pubmed/31959018 http://dx.doi.org/10.1177/1534735419900798 |
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author | Takaku, Shun Shimizu, Masumi Takahashi, Hidemi |
author_facet | Takaku, Shun Shimizu, Masumi Takahashi, Hidemi |
author_sort | Takaku, Shun |
collection | PubMed |
description | Although the Japanese traditional herbal medicine (Kampo), Juzentaihoto (JTT), has been reported to have antitumor effects in several tumor models, its role in tumor immunology remains controversial. In the present study, we tested whether oral administration of JTT enhances antitumor immunity in CD1d(−/−) mice, in which immunosuppression was partially relieved due to the lack of NKT cells. In a subcutaneous murine syngeneic CT26 colorectal tumor model, JTT had no impact on tumor growth in wild type (WT) BALB/c mice. However, the growth rate of tumors was significantly slower in CD1d(−/−) mice than in WT mice. Surprisingly, JTT significantly delayed tumor growth in such CD1d(−/−) mice. In vivo depletion of CD8(+) T cells revealed that CD8(+) T cells are required for JTT’s antitumor activity. Moreover, tumor-reactive cytotoxic T-lymphocytes were detected exclusively in JTT-treated mice with well-controlled tumors. JTT did not affect the number of tumor-infiltrating CD4(+) regulatory T cells. On the contrary, JTT increased the degranulation marker CD107a(+) CD8(+) T cells and decreased Ly6G(+) Ly6C(lo) polymorphonuclear myeloid-derived suppressor cells in tumor-infiltrating lymphocytes, most probably contributing to the suppression of tumor growth in JTT-treated mice. Nonetheless, JTT had no impact on the proportion of monocytic myeloid-derived suppressor cells. In conclusion, our results indicate that in the absence of NKT cells, JTT augments antitumor immunity by CD8(+) T cells, suggesting that this Kampo medicine is a promising anticancer adjuvant when negative immune regulation is partially relieved. |
format | Online Article Text |
id | pubmed-6974754 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | SAGE Publications |
record_format | MEDLINE/PubMed |
spelling | pubmed-69747542020-01-31 Japanese Kampo Medicine Juzentaihoto Enhances Antitumor Immunity in CD1d(−/−) Mice Lacking NKT Cells Takaku, Shun Shimizu, Masumi Takahashi, Hidemi Integr Cancer Ther Research Article Although the Japanese traditional herbal medicine (Kampo), Juzentaihoto (JTT), has been reported to have antitumor effects in several tumor models, its role in tumor immunology remains controversial. In the present study, we tested whether oral administration of JTT enhances antitumor immunity in CD1d(−/−) mice, in which immunosuppression was partially relieved due to the lack of NKT cells. In a subcutaneous murine syngeneic CT26 colorectal tumor model, JTT had no impact on tumor growth in wild type (WT) BALB/c mice. However, the growth rate of tumors was significantly slower in CD1d(−/−) mice than in WT mice. Surprisingly, JTT significantly delayed tumor growth in such CD1d(−/−) mice. In vivo depletion of CD8(+) T cells revealed that CD8(+) T cells are required for JTT’s antitumor activity. Moreover, tumor-reactive cytotoxic T-lymphocytes were detected exclusively in JTT-treated mice with well-controlled tumors. JTT did not affect the number of tumor-infiltrating CD4(+) regulatory T cells. On the contrary, JTT increased the degranulation marker CD107a(+) CD8(+) T cells and decreased Ly6G(+) Ly6C(lo) polymorphonuclear myeloid-derived suppressor cells in tumor-infiltrating lymphocytes, most probably contributing to the suppression of tumor growth in JTT-treated mice. Nonetheless, JTT had no impact on the proportion of monocytic myeloid-derived suppressor cells. In conclusion, our results indicate that in the absence of NKT cells, JTT augments antitumor immunity by CD8(+) T cells, suggesting that this Kampo medicine is a promising anticancer adjuvant when negative immune regulation is partially relieved. SAGE Publications 2020-01-20 /pmc/articles/PMC6974754/ /pubmed/31959018 http://dx.doi.org/10.1177/1534735419900798 Text en © The Author(s) 2020 https://creativecommons.org/licenses/by-nc/4.0/ This article is distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 License (https://creativecommons.org/licenses/by-nc/4.0/) which permits non-commercial use, reproduction and distribution of the work without further permission provided the original work is attributed as specified on the SAGE and Open Access pages (https://us.sagepub.com/en-us/nam/open-access-at-sage). |
spellingShingle | Research Article Takaku, Shun Shimizu, Masumi Takahashi, Hidemi Japanese Kampo Medicine Juzentaihoto Enhances Antitumor Immunity in CD1d(−/−) Mice Lacking NKT Cells |
title | Japanese Kampo Medicine Juzentaihoto Enhances Antitumor Immunity in
CD1d(−/−) Mice Lacking NKT Cells |
title_full | Japanese Kampo Medicine Juzentaihoto Enhances Antitumor Immunity in
CD1d(−/−) Mice Lacking NKT Cells |
title_fullStr | Japanese Kampo Medicine Juzentaihoto Enhances Antitumor Immunity in
CD1d(−/−) Mice Lacking NKT Cells |
title_full_unstemmed | Japanese Kampo Medicine Juzentaihoto Enhances Antitumor Immunity in
CD1d(−/−) Mice Lacking NKT Cells |
title_short | Japanese Kampo Medicine Juzentaihoto Enhances Antitumor Immunity in
CD1d(−/−) Mice Lacking NKT Cells |
title_sort | japanese kampo medicine juzentaihoto enhances antitumor immunity in
cd1d(−/−) mice lacking nkt cells |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6974754/ https://www.ncbi.nlm.nih.gov/pubmed/31959018 http://dx.doi.org/10.1177/1534735419900798 |
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