Laboratory of Nano- and Translational Medicine, Carolina Center for Cancer Nanotechnology Excellence, Carolina Institute of Nanomedicine, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Department of Radiation Oncology, Lineberger Comprehensive Cancer Center, University of North Carolina at Chapel Hill, Chapel Hill, NC 27599, USA.
Sci Adv. 2020 Jul 3;6(27):eaba8564. doi: 10.1126/sciadv.aba8564. eCollection 2020 Jul.
Activation of the innate immune system and natural killer (NK) cells has been a key effort in cancer immunotherapy research. Here, we report a nanoparticle-based trispecific NK cell engager (nano-TriNKE) platform that can target epidermal growth factor receptor (EGFR)-overexpressing tumors and promote the recruitment and activation of NK cells to eradicate these cancer cells. Moreover, the nanoengagers can deliver cytotoxic chemotherapeutics to further improve their therapeutic efficacy. We have demonstrated that effective NK cell activation can be achieved by the spatiotemporal coactivation of CD16 and 4-1BB stimulatory molecules on NK cells with nanoengagers, and the nanoengagers are more effective than free antibodies. We also show that biological targeting, either through radiotherapy or EGFR, is critical to the therapeutic effects of nanoengagers. Last, EGFR-targeted nanoengagers can augment both NK-activating agents and chemotherapy (epirubicin) as highly effective anticancer agents, providing robust chemoimmunotherapy.
先天免疫系统和自然杀伤 (NK) 细胞的激活一直是癌症免疫治疗研究的重点。在这里,我们报告了一种基于纳米颗粒的三特异性 NK 细胞衔接器 (nano-TriNKE) 平台,该平台可以靶向表皮生长因子受体 (EGFR) 过表达的肿瘤,并促进 NK 细胞的募集和激活,以消灭这些癌细胞。此外,纳米衔接器还可以递送细胞毒性化疗药物,以进一步提高其治疗效果。我们已经证明,通过纳米衔接器时空共激活 NK 细胞上的 CD16 和 4-1BB 刺激分子,可以实现有效的 NK 细胞激活,并且纳米衔接器比游离抗体更有效。我们还表明,生物靶向,无论是通过放射治疗还是 EGFR,对于纳米衔接器的治疗效果都至关重要。最后,EGFR 靶向的纳米衔接器可以增强 NK 激活剂和化疗药物(表阿霉素)作为高效的抗癌药物,提供强大的化疗免疫治疗。