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Huang Lian Jie Du Decoction enhances the anti-tumor efficacy of immune checkpoint inhibitors by activating TLR7/8 signalling in melanoma.

Authors :
Liu, Suqing
Zhang, Yaohua
Zhu, Xiaohua
He, Shan
Liu, Xiao
Lv, Xiang
Zuo, Fuguo
Wu, Jinfeng
Source :
BMC Complementary Medicine & Therapies; 4/11/2024, Vol. 24 Issue 1, p1-12, 12p
Publication Year :
2024

Abstract

Background: The clinical application of immune checkpoint inhibitors (ICIs) is limited by their drug resistance, necessitating the development of ICI sensitizers to improve cancer immunotherapy outcomes. Huang Lian Jie Du Decoction (HLJD, Oren-gedoku-to in Japanese, Hwangryunhaedok-tang in Korean), a famous traditional Chinese medicinal prescription, has exhibited potential in the field of cancer treatment. This study aims to investigate the impact of HLJD on the efficacy of ICIs in melanoma and elucidate the underlying mechanisms. Methods: The potential synergistic effects of HLJD and ICIs were investigated on the tumor-bearing mice model of B16F10 melanoma, and the tumor infiltration of immune cells was tested by flow cytometry. The differential gene expression in tumors between HLJD and ICIs group and ICIs alone group were analyzed by RNA-seq. The effects of HLJD on oxidative stress, TLR7/8, and type I interferons (IFN-Is) signaling were further validated by immunofluorescence, PCR array, and immunochemistry in tumor tissue. Results: HLJD enhanced the anti-tumor effect of ICIs, significantly inhibited tumor growth, and prolonged the survival duration in melanoma. HLJD increased the tumor infiltration of anti-tumor immune cells, especially DCs, CD4<superscript>+</superscript> T cells and CD8<superscript>+</superscript>T cells. Mechanically, HLJD activated the oxidative stress and TLR7/8 signaling pathway and IFN-Is-related genes in tumors. Conclusions: HLJD enhanced the therapeutic benefits of ICIs in melanoma, through increasing reactive oxygen species (ROS), promoting the TLR7/8 pathway, and activating IFN-Is signaling, which in turn activated DCs and T cells. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
26627671
Volume :
24
Issue :
1
Database :
Complementary Index
Journal :
BMC Complementary Medicine & Therapies
Publication Type :
Academic Journal
Accession number :
176562191
Full Text :
https://doi.org/10.1186/s12906-024-04444-y