Japanese Kampo Medicine Juzentaihoto Enhances Antitumor Immunity in CD1d Mice Lacking NKT Cells.

Integr Cancer Ther

Department of Microbiology and Immunology, Nippon Medical School, Bunkyo-ku, Tokyo, Japan.

Published: March 2020

AI Article Synopsis

  • - The study investigates the effects of Juzentaihoto (JTT), a Japanese herbal medicine, on antitumor immunity in CD1d mice lacking NKT cells, finding that JTT significantly delays tumor growth in these mice compared to wild type mice.
  • - JTT's antitumor activity relies on the presence of CD8 T cells, which are necessary for its effectiveness, while not affecting the number of regulatory CD4 T cells or monocytic myeloid-derived suppressor cells.
  • - The results suggest that JTT enhances antitumor immunity by increasing the activity of CD8 T cells and decreasing certain suppressor cells, indicating its potential as an anticancer treatment when immune regulation is reduced.

Article Abstract

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 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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6974754PMC
http://dx.doi.org/10.1177/1534735419900798DOI Listing

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