复方苦参注射液通过 TNFR1 缓解肿瘤相关巨噬细胞介导的免疫抑制作用,并增强索拉非尼对肝细胞癌的敏感性。
Compound kushen injection relieves tumor-associated macrophage-mediated immunosuppression through TNFR1 and sensitizes hepatocellular carcinoma to sorafenib.
机构信息
CAS Key Laboratory of Nutrition, Metabolism and Food safety, Shanghai Institute of Nutrition and Health, Shanghai Institutes for Biological Sciences, University of Chinese Academy of Sciences, Chinese Academy of Sciences, Shanghai, China.
State Key Laboratory of Oncogenes and Related Genes, Center for Single-Cell Omics, School of Public Health, Shanghai Jiao Tong University School of Medicine, Shanghai, China.
出版信息
J Immunother Cancer. 2020 Mar;8(1). doi: 10.1136/jitc-2019-000317.
BACKGROUND
There is an urgent need for effective treatments for hepatocellular carcinoma (HCC). Immunotherapy is promising especially when combined with traditional therapies. This study aimed to investigate the immunomodulatory function of an approved Chinese medicine formula, compound kushen injection (CKI), and its anti-HCC efficiency in combination with low-dose sorafenib.
METHODS
Growth of two murine HCC cells was evaluated in an orthotopic model, a subcutaneous model, two postsurgical recurrence model, and a tumor rechallenge model with CKI and low-dose sorafenib combination treatment. In vivo macrophage or CD8 T cell depletion and in vitro primary cell coculture models were used to determine the regulation of CKI on macrophages and CD8 T cells.
RESULTS
CKI significantly enhanced the anticancer activity of sorafenib at a subclinical dose with no obvious side effects. CKI and sorafenib combination treatment prevented the postsurgical recurrence and rechallenged tumor growth. Further, we showed that CKI activated proinflammatory responses and relieved immunosuppression of tumor-associated macrophages in the HCC microenvironment by triggering tumor necrosis factor receptor superfamily member 1 (TNFR1)-mediated NF-κB and p38 MAPK signaling cascades. CKI-primed macrophages significantly promoted the proliferation and the cytotoxic ability of CD8 T cells and decreased the exhaustion, which subsequently resulted in apoptosis of HCC cells.
CONCLUSIONS
CKI acts on macrophages and CD8 T cells to reshape the immune microenvironment of HCC, which improves the therapeutic outcomes of low-dose sorafenib and avoids adverse chemotherapy effects. Our study shows that traditional Chinese medicines with immunomodulatory properties can potentiate chemotherapeutic drugs and provide a promising approach for HCC treatment.
背景
肝细胞癌(HCC)亟需有效的治疗方法。免疫疗法具有广阔的应用前景,尤其是与传统疗法联合应用时。本研究旨在探讨一种已上市的中药制剂复方苦参注射液(CKI)的免疫调节功能,及其与低剂量索拉非尼联合应用的抗 HCC 效果。
方法
采用原位模型、皮下模型、两种术后复发模型和肿瘤再挑战模型,评估 CKI 和低剂量索拉非尼联合治疗对两种鼠 HCC 细胞的生长抑制作用。通过体内巨噬细胞或 CD8 T 细胞耗竭和体外原代细胞共培养模型,研究 CKI 对巨噬细胞和 CD8 T 细胞的调控作用。
结果
CKI 可增强低剂量索拉非尼的抗癌活性,且无明显副作用。CKI 和索拉非尼联合治疗可预防术后复发和再挑战肿瘤生长。进一步研究表明,CKI 通过触发肿瘤坏死因子受体超家族成员 1(TNFR1)介导的 NF-κB 和 p38 MAPK 信号通路,激活 HCC 微环境中促炎反应,缓解肿瘤相关巨噬细胞的免疫抑制作用。CKI 激活的巨噬细胞可显著促进 CD8 T 细胞的增殖和细胞毒性作用,降低其衰竭程度,从而诱导 HCC 细胞凋亡。
结论
CKI 通过作用于巨噬细胞和 CD8 T 细胞,重塑 HCC 的免疫微环境,增强低剂量索拉非尼的治疗效果,避免了化疗的不良反应。本研究表明,具有免疫调节特性的中药可增强化疗药物的疗效,为 HCC 的治疗提供了一种有前景的方法。