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YIV-906 通过增强肿瘤微环境中的适应性和先天免疫来增强抗 PD1 作用,从而对抗肝细胞癌。

YIV-906 potentiated anti-PD1 action against hepatocellular carcinoma by enhancing adaptive and innate immunity in the tumor microenvironment.

机构信息

Department of Pharmacology, Yale University School of Medicine, 333 Cedar Street, SHM B254, New Haven, CT, 06510, USA.

Department of Cardiology and Health Care, Guanganmen Hospital, China Academy of Chinese Medical Sciences, Beijing, China.

出版信息

Sci Rep. 2021 Jun 29;11(1):13482. doi: 10.1038/s41598-021-91623-3.

DOI:10.1038/s41598-021-91623-3
PMID:34188068
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8242098/
Abstract

YIV-906 (PHY906) is a standardized botanical cancer drug candidate developed with a systems biology approach-inspired by a traditional Chinese herbal formulation, historically used to treat gastrointestinal symptoms including diarrhea, nausea and vomiting. In combination with chemotherapy and/or radiation therapy, preclinical and clinical results suggest that YIV-906 has the potential to prolong survival and improve quality of life for cancer patients. Here, we demonstrated that YIV-906 plus anti-PD1 could eradicate all Hepa 1-6 tumors in all tumor bearing mice. YIV-906 was found to have multiple mechanisms of action to enhance adaptive and innate immunity. In combination, YIV-906 reduced PD1 or counteracted PD-L1 induction caused by anti-PD1 which led to higher T-cell activation gene expression of the tumor. In addition, YIV-906 could reduce immune tolerance by modulating IDO activity and reducing monocytic MDSC of the tumor. The combination of anti-PD1 and YIV-906 generated acute inflammation in the tumor microenvironment with more M1-like macrophages. YIV-906 could potentiate the action of interferon gamma (IFNg) to increase M1-like macrophage polarization while inhibiting IL4 action to decrease M2 macrophage polarization. Flavonoids from YIV-906 were responsible for modulating IDO activity and potentiating IFNg action in M1-like macrophage polarization. In conclusion, YIV-906 could act as an immunomodulator and enhance the innate and adaptive immune response and potentiate anti-tumor activity for immunotherapies to treat cancer.

摘要

YIV-906(PHY906)是一种采用系统生物学方法开发的标准化植物癌症药物候选物,其灵感来自一种传统的中草药配方,历史上用于治疗胃肠道症状,包括腹泻、恶心和呕吐。与化疗和/或放射治疗联合使用,临床前和临床研究结果表明,YIV-906有可能延长癌症患者的生存时间并提高生活质量。在这里,我们证明了 YIV-906 加抗 PD1 可以消灭所有荷瘤小鼠的 Hepa 1-6 肿瘤。YIV-906 具有多种增强适应性和先天免疫的作用机制。联合使用时,YIV-906 减少了抗 PD1 引起的 PD1 或拮抗 PD-L1 的诱导,从而导致肿瘤中 T 细胞激活基因表达更高。此外,YIV-906 通过调节 IDO 活性和减少肿瘤中的单核细胞 MDSC 来减少免疫耐受。抗 PD1 和 YIV-906 的联合作用在肿瘤微环境中产生了急性炎症,具有更多 M1 样巨噬细胞。YIV-906 可以增强干扰素 γ(IFNg)的作用,增加 M1 样巨噬细胞极化,同时抑制 IL4 作用,减少 M2 巨噬细胞极化。YIV-906 中的类黄酮负责调节 IDO 活性并增强 M1 样巨噬细胞极化中的 IFNg 作用。总之,YIV-906 可以作为一种免疫调节剂,增强先天和适应性免疫反应,并增强免疫疗法治疗癌症的抗肿瘤活性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c035/8242098/9a1cbbf0321b/41598_2021_91623_Fig6_HTML.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c035/8242098/8965bb778c3c/41598_2021_91623_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c035/8242098/9a1cbbf0321b/41598_2021_91623_Fig6_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c035/8242098/41b520ac2a2e/41598_2021_91623_Fig1_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c035/8242098/5a1334ec34e6/41598_2021_91623_Fig2_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c035/8242098/ba6d97050892/41598_2021_91623_Fig3_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c035/8242098/49bd1cc909fe/41598_2021_91623_Fig4_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c035/8242098/8965bb778c3c/41598_2021_91623_Fig5_HTML.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/c035/8242098/9a1cbbf0321b/41598_2021_91623_Fig6_HTML.jpg

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本文引用的文献

1
Trial watch: IDO inhibitors in cancer therapy.试验观察:癌症治疗中的吲哚胺2,3-双加氧酶抑制剂
Oncoimmunology. 2020 Jun 14;9(1):1777625. doi: 10.1080/2162402X.2020.1777625.
2
Epacadostat plus pembrolizumab versus placebo plus pembrolizumab in patients with unresectable or metastatic melanoma (ECHO-301/KEYNOTE-252): a phase 3, randomised, double-blind study.依匹单抗联合帕博利珠单抗对比安慰剂联合帕博利珠单抗用于不可切除或转移性黑色素瘤患者(ECHO-301/KEYNOTE-252):一项 III 期、随机、双盲研究。
Lancet Oncol. 2019 Aug;20(8):1083-1097. doi: 10.1016/S1470-2045(19)30274-8. Epub 2019 Jun 17.
3
Mechanism Based Quality Control (MBQC) of Herbal Products: A Case Study YIV-906 (PHY906).
用于治疗肝胆系统癌症的传统中药:从临床证据到药物研发
Mol Cancer. 2024 Oct 1;23(1):218. doi: 10.1186/s12943-024-02136-2.
4
A single arm phase 2 clinical trial of YIV-906 with neoadjuvant concurrent chemo-radiation therapy in patients with locally advanced rectal cancer.一项关于YIV-906联合新辅助同步放化疗用于局部晚期直肠癌患者的单臂2期临床试验。
J Gastrointest Oncol. 2024 Jun 30;15(3):1050-1059. doi: 10.21037/jgo-24-23. Epub 2024 Jun 25.
5
Crithmum maritimum Extract Restores Lipid Homeostasis and Metabolic Profile of Liver Cancer Cells to a Normal Phenotype.滨海獐牙菜提取物可恢复肝癌细胞的脂类稳态和代谢特征,使其向正常表型转化。
Plant Foods Hum Nutr. 2024 Jun;79(2):417-424. doi: 10.1007/s11130-024-01188-5. Epub 2024 May 6.
6
Huang Lian Jie Du Decoction enhances the anti-tumor efficacy of immune checkpoint inhibitors by activating TLR7/8 signalling in melanoma.黄连解毒汤通过激活 TLR7/8 信号通路增强黑色素瘤免疫检查点抑制剂的抗肿瘤疗效。
BMC Complement Med Ther. 2024 Apr 11;24(1):156. doi: 10.1186/s12906-024-04444-y.
7
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Int J Mol Sci. 2023 Aug 10;24(16):12630. doi: 10.3390/ijms241612630.
基于机制的草药产品质量控制(MBQC):以YIV-906(PHY906)为例的案例研究
Front Pharmacol. 2018 Nov 19;9:1324. doi: 10.3389/fphar.2018.01324. eCollection 2018.
4
Anti-PD-1 therapy redirects macrophages from an M2 to an M1 phenotype inducing regression of OS lung metastases.抗 PD-1 治疗将巨噬细胞从 M2 表型重定向为 M1 表型,从而诱导 OS 肺转移瘤消退。
Cancer Med. 2018 Jun;7(6):2654-2664. doi: 10.1002/cam4.1518. Epub 2018 May 7.
5
Rapid activation of tumor-associated macrophages boosts preexisting tumor immunity.快速激活肿瘤相关巨噬细胞可增强预先存在的肿瘤免疫。
J Exp Med. 2018 Mar 5;215(3):859-876. doi: 10.1084/jem.20171440. Epub 2018 Feb 7.
6
Lenvatinib versus sorafenib in first-line treatment of patients with unresectable hepatocellular carcinoma: a randomised phase 3 non-inferiority trial.乐伐替尼与索拉非尼用于不可切除肝细胞癌患者一线治疗的比较:一项随机、III 期非劣效性试验。
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Lancet. 2017 Jun 24;389(10088):2492-2502. doi: 10.1016/S0140-6736(17)31046-2. Epub 2017 Apr 20.
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Mol Ther. 2017 Jul 5;25(7):1665-1675. doi: 10.1016/j.ymthe.2017.02.007. Epub 2017 Mar 9.