Eden Y Zewdie, George M Edwards, Debra M Hunter, Henry Shelton Earp, Alisha Holtzhausen
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引用次数: 0
摘要
检查点抑制剂,特别是抗-PD-1,在治疗转移性黑色素瘤方面取得了成功;但是,有些患者会产生抗药性。树突状细胞(DC)在启动免疫反应中发挥着关键作用,但在某些情况下它们会变得无效。我们研究了MerTK(一种负责髓系细胞清除死亡细胞的受体酪氨酸激酶)在肿瘤微环境中调控树突状细胞功能和新陈代谢中的作用。对抗PD-1耐药的肿瘤显示出MerTK+ DCs水平的升高。在体外用凋亡的黑色素瘤死细胞处理野生型直流细胞会导致 MerTK 表达增加、线粒体呼吸和脂肪酸氧化升高以及 T 细胞刺激能力降低,这些都是功能失调型直流细胞的特征。相比之下,死亡细胞对缺失 MerTK 的直流细胞的新陈代谢影响有限,相反,直流细胞保持了抗原呈递和刺激表型。在选择性消减直流区MerTK的小鼠中,抗PD-1减缓肿瘤进展和诱导特异性T细胞浸润的效果明显增强,这表明有可能以MerTK为治疗靶点,调节直流代谢和功能,加强抗PD-1治疗。
MerTK Induces Dysfunctional Dendritic Cells by Metabolic Reprogramming.
Checkpoint inhibitors, specifically anti-programmed cell death protein 1 (PD1), have shown success in treating metastatic melanoma; however, some patients develop resistance. Dendritic cells (DC) play a key role in initiating an immune response, but in certain circumstances they become ineffective. We investigated the role of MerTK, a receptor tyrosine kinase responsible for myeloid cell clearance of dead cells, in the regulation of DC function and metabolism in the tumor microenvironment. Tumors resistant to anti-PD1 exhibited increased levels of MerTK+ DCs. Treating wild-type DCs with apoptotic melanoma cells in vitro resulted in increased MerTK expression, elevated mitochondrial respiration and fatty acid oxidation, and reduced T-cell stimulatory capacity, all characteristics of dysfunctional DCs. In contrast, dead cells had only limited effect on the metabolism of MerTK-deficient DCs, which instead maintained an antigen-presenting, stimulatory phenotype. The efficacy of anti-PD1 to slow tumor progression and induce antigen specific T-cell infiltration was markedly increased in mice with selective ablation of MerTK in the DC compartment, suggesting the possibility of therapeutically targeting MerTK to modulate DC metabolism and function and enhance anti-PD1 therapy.
期刊介绍:
Cancer Immunology Research publishes exceptional original articles showcasing significant breakthroughs across the spectrum of cancer immunology. From fundamental inquiries into host-tumor interactions to developmental therapeutics, early translational studies, and comprehensive analyses of late-stage clinical trials, the journal provides a comprehensive view of the discipline. In addition to original research, the journal features reviews and opinion pieces of broad significance, fostering cross-disciplinary collaboration within the cancer research community. Serving as a premier resource for immunology knowledge in cancer research, the journal drives deeper insights into the host-tumor relationship, potent cancer treatments, and enhanced clinical outcomes.
Key areas of interest include endogenous antitumor immunity, tumor-promoting inflammation, cancer antigens, vaccines, antibodies, cellular therapy, cytokines, immune regulation, immune suppression, immunomodulatory effects of cancer treatment, emerging technologies, and insightful clinical investigations with immunological implications.