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YIV-906增强T细胞的活化T细胞核因子(NFAT)活性,并促进免疫检查点阻断抗体作用和嵌合抗原受体T细胞(CAR T细胞)活性。

YIV-906 enhances nuclear factor of activated T-cells (NFAT) activity of T cells and promotes immune checkpoint blockade antibody action and CAR T-cell activity.

作者信息

Lam Wing, Hu Rong, Liu Shwu-Huey, Cheng Peikwen, Cheng Yung-Chi

机构信息

Department of Pharmacology, Yale University School of Medicine, New Haven, CN, United States.

Yiviva Inc, New York, NY, United States.

出版信息

Front Pharmacol. 2023 Jan 4;13:1095186. doi: 10.3389/fphar.2022.1095186. eCollection 2022.

DOI:10.3389/fphar.2022.1095186
PMID:36686648
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9846171/
Abstract

YIV-906 is a systems biology botanical cancer drug, inspired by a traditional Chinese herbal formulation. Results from eight Phase I/II to II clinical studies demonstrated the potential of YIV-906 to prolong survival and improve the quality of life of cancer patients. As an immunomodulator in the tumor microenvironment, YIV-906 can turn cold tumors hot and potentiate anti-tumor activity for different classes of anticancer agents; and as a cytoprotector in the GI, YIV-906 can reduce non-hematological side effects and speed up damaged tissue recovery. YIV-906 enhanced anti-PD1 action against hepatoma in mice by stimulating both innate and adaptive immunity. In a Jurkat cell-staphylococcal superantigen E (SEE)-Raji cell culture model, YIV-906 promoted T cell activation with upregulation of CD69 by enhancing NFAT activity, with or without PD1-PD-L1 interaction. YIV-906 could trigger the phosphorylation of TCR downstream signaling cascades without the involvement of TCR. YIV-906 could inhibit SHP1 and SHP2 activities, which dephosphorylates TCR downstream proteins due to the PD1-PD-L1 interaction. Therefore, YIV-906 could enhance anti-PD1 action to rescue the depressed NFAT activity of Jurkat cells due to the PD1-PD-L1 interaction. In addition, YIV-906 enhanced the NFAT activity and killing capability of Jurkat cells expressing chimeric antigen receptor (CAR-CD19CD3z) toward CD19 expressing cells, such as Raji cells, with or without PD1-PD-L1 overexpression. Ingredient herb () of YIV-906 and some compounds were found to play key roles in these activities. In conclusion, YIV-906 modulates adaptive immunity by activating T effector cells mainly through its action on SHP1/2. YIV-906 could also facilitate immune checkpoint blockade therapy or CAR-T cell therapy for cancer treatment.

摘要

YIV-906是一种受传统中药配方启发的系统生物学植物抗癌药物。八项从I/II期到II期临床研究的结果表明,YIV-906具有延长癌症患者生存期和改善其生活质量的潜力。作为肿瘤微环境中的一种免疫调节剂,YIV-906可使冷肿瘤变热,并增强不同类型抗癌药物的抗肿瘤活性;作为胃肠道中的一种细胞保护剂,YIV-906可减少非血液学副作用并加速受损组织的恢复。YIV-906通过刺激先天性和适应性免疫增强了抗PD1对小鼠肝癌的作用。在Jurkat细胞-葡萄球菌超抗原E(SEE)-Raji细胞培养模型中,无论有无PD1-PD-L1相互作用,YIV-906通过增强NFAT活性促进T细胞活化并上调CD69。YIV-906可在不涉及TCR的情况下触发TCR下游信号级联的磷酸化。YIV-906可抑制SHP1和SHP2的活性,而SHP1和SHP2的活性会因PD1-PD-L1相互作用使TCR下游蛋白去磷酸化。因此,YIV-906可增强抗PD1作用,以挽救因PD1-PD-L1相互作用导致的Jurkat细胞中NFAT活性降低。此外,无论有无PD1-PD-L1过表达,YIV-906均可增强表达嵌合抗原受体(CAR-CD19CD3z)的Jurkat细胞对表达CD19的细胞(如Raji细胞)的NFAT活性和杀伤能力。发现YIV-906的成分草药()和一些化合物在这些活性中起关键作用。总之,YIV-906主要通过作用于SHP1/2激活T效应细胞来调节适应性免疫。YIV-906还可促进免疫检查点阻断疗法或CAR-T细胞疗法用于癌症治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca87/9846171/ca28f9ed867d/fphar-13-1095186-g007.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca87/9846171/ca28f9ed867d/fphar-13-1095186-g007.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca87/9846171/da6df4bea4e6/fphar-13-1095186-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca87/9846171/011cd79f0c36/fphar-13-1095186-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca87/9846171/07b3b936bf30/fphar-13-1095186-g003.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca87/9846171/eba535f6988d/fphar-13-1095186-g005.jpg
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https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ca87/9846171/ca28f9ed867d/fphar-13-1095186-g007.jpg

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