Divisions of Hematology and Medical Oncology, Department of Medicine, University of California San Francisco, San Francisco, California.
Parker Institute for Cancer Immunotherapy, San Francisco, California.
Clin Cancer Res. 2022 Jan 1;28(1):5-12. doi: 10.1158/1078-0432.CCR-21-1193. Epub 2021 Jul 20.
The impact of liver metastases on immune checkpoint-inhibitor effectiveness in patients with solid-tumor malignancies has been the focus of several recent clinical and translational studies. We review the literature describing the immune functions of the liver and particularly the mechanistic observations in these studies. The initial clinical observation was that pembrolizumab appeared to be much less effective in melanoma and non-small cell lung cancer (NSCLC) patients with liver metastasis. Subsequently other clinical studies have extended and reported similar findings with programmed death-1 (PD-1) and programmed death ligand-1 (PD-L1) inhibitors in many cancers. Two recent translational studies in animal models have dissected the mechanism of this systemic immune suppression. In both studies CD11b suppressive macrophages generated by liver metastasis in a two-site MC38 model appear to delete CD8 T cells in a FasL-dependent manner. In addition, regulatory T-cell (Treg) activation was observed and contributed to the distal immunosuppression. Finally, we discuss some of the interventions reported to address liver immune suppression, such as radiation therapy, combination checkpoint blockade, and Treg depletion.
肝转移对实体瘤恶性肿瘤患者免疫检查点抑制剂疗效的影响一直是最近几项临床和转化研究的重点。我们回顾了描述肝脏免疫功能的文献,特别是这些研究中的机制观察。最初的临床观察是,在患有肝转移的黑色素瘤和非小细胞肺癌(NSCLC)患者中,pembrolizumab 的疗效似乎要低得多。随后,其他临床研究也扩展并报告了在许多癌症中使用程序性死亡受体-1(PD-1)和程序性死亡配体-1(PD-L1)抑制剂的类似发现。最近两项在动物模型中的转化研究剖析了这种全身免疫抑制的机制。在两项研究中,MC38 模型中的肝转移生成的 CD11b 抑制性巨噬细胞似乎以 FasL 依赖的方式删除 CD8 T 细胞。此外,观察到调节性 T 细胞(Treg)的激活,并导致远端免疫抑制。最后,我们讨论了一些已报道的干预措施,以解决肝免疫抑制问题,如放射治疗、联合检查点阻断和 Treg 耗竭。