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含灵芝的草药混合物通过 CD8(+) T 细胞介导的治疗性抗肿瘤作用

英文原题:CD8(+) T Cell-Mediated Therapeutic Antitumor Effect of an Herbal Mixture Containing Ganoderma lucidum.

查看英文原题

CD8(+) T Cell-Mediated Therapeutic Antitumor Effect of an Herbal Mixture Containing Ganoderma lucidum.

PubMed 2023/04/28(内容时间) Evid Based Complement Alternat Med

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中文摘要

尽管汉方——一种日本传统草药——在实验动物体内有助于控制肿瘤生长,但大多数抗肿瘤作用为预防性而非治疗性。本研究旨在确定一种含有灵芝的草药混合物(WTMCGEP;包含紫藤、泽泻、肉豆蔻、薏苡仁、灵芝、树舌和石榴)经口给药后,在皮下小鼠CT26结直肠肿瘤模型中是否表现出体内肿瘤生长的治疗作用,该混合物在日本被经验性地用于癌症患者的姑息治疗。体外肿瘤实验显示,WTMCGEP提取物对肿瘤生长具有一定的直接抑制作用。在野生型BALB/c小鼠中,WTMCGEP未表现出任何体内抗肿瘤作用。

然而,在BALB-CD1d -/- 小鼠中,由于缺乏抗肿瘤I型和免疫抑制II型自然杀伤T(NKT)细胞而部分减轻了免疫抑制,WTMCGEP可治疗性地抑制肿瘤生长。CD8 + T细胞清除显著加速了WTMCGEP小鼠的肿瘤生长;因此,其抗肿瘤活性主要以CD8 + T细胞依赖的方式发挥。关于荷瘤CD1d -/- 小鼠中的免疫抑制细胞,WTMCGEP未影响肿瘤浸润性CD4 + 和Forkhead box protein 3 + 调节性T细胞的数量。

然而,它减少了瘤内和脾脏中的Ly6G + Ly6C lo 多形核髓源性抑制细胞,这些细胞最可能参与了与这些小鼠瘤内CD107a + CD8 + T细胞频率升高相关的肿瘤生长抑制。

总体而言,这些数据表明NKT细胞的缺陷促使WTMCGEP主要通过CD8+ T细胞发挥治疗性抗肿瘤作用。我们的工作是首次科学地证明WTMCGEP对肿瘤免疫的贡献。

展开英文摘要原文

Although Kampo-a traditional Japanese herbal medicine-contributes in the control of tumor growth in vivo in experimental animals, most of the antitumor effects are prophylactic and not therapeutic.

In this study, we determined whether oral administration of an herbal mixture containing Ganoderma lucidum (WTMCGEP; Wisteria floribunda , Trapae fructus , Myristica fragrans , Coicis semen , Ganoderma lucidum , Elfvingia applanata , and Punica granatum ), anecdotally used in Japan for the palliative care of patients with cancer, exhibits a therapeutic effect on tumor growth in vivo in a hypodermic murine CT26 colorectal tumor model.

An in vitro tumor assay revealed that WTMCGEP extract has some direct influence over suppression of tumor growth. In wild-type BALB/c mice, WTMCGEP did not show any antitumor effect in vivo .

However, in BALB-CD1d -/- mice with partly mitigated immunosuppression by reason of them being devoid of both antitumoral type I and immunosuppressive type II natural killer T (NKT) cells, WTMCGEP therapeutically suppressed tumor growth.

CD8 + T cell depletion significantly accelerated tumor growth in WTMCGEP mice; therefore, its antitumor activity was primarily in a CD8 + T cell-dependent manner. Regarding immunosuppressive cells in tumor-bearing CD1d -/- mice, WTMCGEP did not influence the abundance of tumor-infiltrating CD4 + and Forkhead box protein 3 + regulatory T cells.

However, it reduced both intratumoral and splenic Ly6G + Ly6C lo polymorphonuclear myeloid-derived suppressor cells, which were most likely involved in tumor growth inhibition related to higher frequency of intratumoral CD107a + CD8 + T cells in these mice.

Overall, these data illustrate that the deficiency of NKT cells urges WTMCGEP to exert a therapeutic antitumor effect mainly through CD8 + T cells.

Our efforts are the first to scientifically demonstrate the WTMCGEP's contribution to tumor immunity.

论文信息

作者
Takaku S、Shimizu M、Morita R
单位
Department of Microbiology and Immunology, Nippon Medical School, Tokyo 113-8602, Japan.Japan
期刊
Evidence-based complementary and alternative medicine : eCAM2023
原文标识
PubMed 37152373 · DOI 10.1155/2023/9630816