Department of Pathology, The Johns Hopkins University School of Medicine, 1550 Orleans St., CRB II - Room 307, Baltimore, MD, 21287, USA.
Division of Pulmonary Medicine, Department of Internal Medicine, Shuang Ho Hospital, Taipei Medical University, New Taipei City, Taiwan.
Cancer Immunol Immunother. 2020 Oct;69(10):2147-2155. doi: 10.1007/s00262-020-02615-7. Epub 2020 May 28.
A major factor impeding the success of numerous therapeutic approaches in cancer is the immunosuppressive nature of the tumor microenvironment (TME). Hence, methods capable of reverting tumor immunosuppression through depletion or reprogramming of myeloid-derived suppressive cells (MDSCs) and regulatory T cells (Tregs) are of great clinical need. Here, we explore NKG2D-Fc as a modality to modulate antitumor immunity through the depletion of immunosuppressive MDSCs and Tregs in the TME. We have generated the NKG2D-Fc fusion protein and characterized its potential to mediate tumor control and overall survival in LL2 and MC38 murine models. Upon treatment of LL2 or MC38 tumor-bearing mice with NKG2D-Fc, we observe significant tumor control and enhanced survival compared to Fc control. When characterizing MDCSs and Tregs from tumor-bearing mice, we observe clear expression of NKG2D-ligand RAE1γ and subsequent binding of NKG2D-Fc fusion protein to both MDSCs and Tregs. Examining the immune profile of mice treated with NKG2D-Fc reveals significant depletion of MDSCs and Tregs in the TME, as well as an increase in NK cells likely due to the reversed suppressive TME. In conclusion, NKG2D-Fc induces antitumor immunity and tumor control through the depletion of MDSCs and Tregs, subsequently providing a niche for the infiltration and expansion of proinflammatory cells, such as NK cells. Strategies capable of modulating the immunosuppressive state in cancer are in high clinical demand. NKG2D-Fc is a simple, single tool capable of depleting both MDSCs and Tregs and should be further investigated as a therapeutic agent for the treatment of cancer.
许多癌症治疗方法之所以未能成功,一个主要因素是肿瘤微环境(TME)的免疫抑制特性。因此,能够通过耗竭或重编程髓系来源的抑制性细胞(MDSCs)和调节性 T 细胞(Tregs)来逆转肿瘤免疫抑制的方法具有重要的临床需求。在这里,我们探索 NKG2D-Fc 通过耗竭 TME 中的免疫抑制性 MDSCs 和 Tregs 来调节抗肿瘤免疫的作用。我们已经生成了 NKG2D-Fc 融合蛋白,并研究了其在 LL2 和 MC38 小鼠模型中控制肿瘤和提高总生存率的潜力。在对携带 LL2 或 MC38 肿瘤的小鼠进行 NKG2D-Fc 治疗后,与 Fc 对照组相比,我们观察到明显的肿瘤控制和生存延长。在对携带肿瘤的小鼠的 MDSCs 和 Tregs 进行特征分析时,我们观察到 NKG2D 配体 RAE1γ 的明显表达,以及 NKG2D-Fc 融合蛋白与 MDSCs 和 Tregs 的后续结合。检查用 NKG2D-Fc 治疗的小鼠的免疫特征表明,TME 中的 MDSCs 和 Tregs 明显耗竭,同时 NK 细胞增加,可能是由于抑制性 TME 逆转。总之,NKG2D-Fc 通过耗竭 MDSCs 和 Tregs 诱导抗肿瘤免疫和肿瘤控制,随后为 NK 细胞等促炎细胞的浸润和扩增提供了一个小生境。能够调节癌症中免疫抑制状态的策略具有很高的临床需求。NKG2D-Fc 是一种简单的单一工具,能够同时耗竭 MDSCs 和 Tregs,应作为癌症治疗的治疗剂进一步研究。