CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Close and Enhance the Cancer-Immunity Cycle by Engineered Dual-Targeted Nano-Adaptors.
Close and Enhance the Cancer-Immunity Cycle by Engineered Dual-Targeted Nano-Adaptors.
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癌症-免疫循环(CIC)提供了一个概念框架,通过靶向系统性免疫中的关键事件来激发有效的抗肿瘤免疫应答。然而,CIC的成功完成往往需要多种治疗方式的协同作用,这要求将其整合到一个统一的系统中,以克服传统联合疗法的局限性。在此,我们提出了一种多模式、可编程的平台,通过双靶向纳米适配器(TNA)纳米技术将多种治疗性生物分子整合到单一制剂中,从而构建多功能的纳米药物和双特异性抗体,以增强CIC。具体而言,TNA纳米药物靶向CIC中的五个关键步骤,包括抗原释放、树突状细胞(DC)成熟、T细胞激活、缓解T细胞耗竭以及肿瘤细胞杀伤。同时,TNA双特异性抗体增强DC-T细胞相互作用以强化适应性免疫,并加强NK-肿瘤细胞相互作用以促进细胞毒性。我们证明TNA能够激发强大的抗肿瘤免疫,根除已建立的肿瘤并抑制转移扩散。由于其模块化和可编程的结构,TNA在免疫治疗及其他领域具有广泛的应用潜力。
The cancer-immunity cycle (CIC) provides a conceptual framework for eliciting effective anti-tumor immune responses by targeting key events in systemic immunity.
However, the successful completion of the CIC often requires the coordinated action of multiple therapeutic modalities, necessitating their integration into a unified system to overcome the limitations of conventional combination therapies.
Here, we present a multimodal and programmable platform that integrates diverse therapeutic biomolecules into single agents, enabling the construction of versatile nanomedicines and bispecific antibodies through dual-targeted nano-adaptor (TNA) nanotechnology to potentiate the CIC.
Specifically, TNA nanomedicines target five critical steps within the CIC, including antigen release, dendritic cell (DC) maturation, T-cell activation, mitigation of T-cell exhaustion, and tumor cell killing. Meanwhile, TNA bispecific antibodies enhance DC-T cell interactions to strengthen adaptive immunity and reinforce NK-tumor cell interactions to promote cytotoxicity.
We demonstrate that TNAs elicit robust anti-tumor immunity, eradicating established tumors and suppressing metastatic dissemination. Owing to their modular and programmable architecture, TNAs hold broad potential for applications in immunotherapy and beyond.
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