CELL INTELLIGENCE · 肿瘤细胞治疗研究
肿瘤细胞治疗研究
英文原题:Nanotechnology Meets Immunotherapy: Crosstalks Against Cancer.
Nanotechnology Meets Immunotherapy: Crosstalks Against Cancer.
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然而,在优化靶向精度、可扩展性和长期安全性方面仍存在挑战。本综述整合了材料科学、免疫学和生物工程领域的突破,为下一代纳米免疫疗法绘制了路线图,倡导患者特异性设计和多模式治疗方案。随着该领域迈向临床成熟,纳米技术有望释放免疫疗法的全部潜力,为适应性、免疫引导且可能实现治愈的癌症疗法铺平道路。
纳米技术与免疫疗法的融合开创了癌症治疗的变革时代,为克服传统疗法的药代动力学局限和免疫逃逸提供了新策略。尽管免疫疗法——涵盖检查点抑制剂、过继性细胞转移和癌症疫苗——已彻底改变肿瘤学,但其疗效仍受限于免疫抑制性肿瘤微环境(TME)、脱靶毒性以及治疗药物生物分布不佳。
本综述阐明工程化纳米颗粒(NPs)如何通过将免疫调节剂、抗原和基因载荷精准递送至靶细胞,同时重编程TME将“冷”肿瘤转化为免疫原性“热”肿瘤微环境,从而重新定义免疫肿瘤学。
通过PubMed、Scopus和Google Scholar进行了文献检索。本综述以叙述性和非系统性的方式进行,重点关注涉及纳米技术增强的癌症免疫治疗的研究。
我们剖析了NPs的理化与功能多样性,重点阐述了基于尺寸、电荷和配体的策略,以增强淋巴结靶向、APC激活和货物持续释放。重点介绍了金属、脂质基和仿生NPs的创新,包括用于增强免疫应答的金和脂质基NPs。此外,我们探讨了组合方法,例如NP介导的检查点抑制剂与化疗药物的共递送,其可放大细胞毒性T细胞应答并减轻全身毒性。临床进展,包括Nab-Paclitaxel和负载mRNA的脂质NPs,凸显了这些平台的转化潜力,试验显示生存改善且不良事件可控。
The convergence of nanotechnology and immunotherapy has ushered in a transformative era in cancer treatment, offering new strategies to overcome pharmacokinetic limitations and immune evasion associated with conventional therapies. While immunotherapy, spanning checkpoint inhibitors, adoptive cell transfer, and cancer vaccines, has revolutionized oncology, its efficacy remains constrained by the immunosuppressive tumor microenvironment (TME), off-target toxicity, and poor biodistribution of therapeutic agents.
This review elucidates how engineered nanoparticles (NPs) are redefining immune-oncology by enabling the precise delivery of immunomodulators, antigens, and genetic payloads to target cells, while reprogramming the TME to convert "cold" tumors into immunogenic "hot" landscapes.
A literature search was conducted using PubMed, Scopus, and Google Scholar. The review was performed in a narrative and non-systematic manner, focusing on studies addressing nanotechnology-enhanced cancer immunotherapy.
We dissect the physicochemical and functional versatility of NPs, emphasizing size-, charge-, and ligand-dependent strategies to enhance lymph node targeting, APC activation, and sustained cargo release. Innovations in metallic, lipid-based, and biomimetic NPs are highlighted, including gold and lipid-based NPs for enhanced immune responses. Furthermore, we explore combinatorial approaches, such as NP-mediated co-delivery of checkpoint inhibitors and chemotherapeutics, which amplify cytotoxic T-cell responses and mitigate systemic toxicity. Clinical advancements, including Nab-Paclitaxel and mRNA-loaded lipid NPs, underscore the translational potential of these platforms, with trials demonstrating improved survival and manageable adverse profiles.
However, challenges persist in optimizing targeting precision, scalability, and long-term safety. Integrating breakthroughs in material science, immunology, and bioengineering, this review charts a roadmap for next-generation nano-immunotherapies, advocating patient-specific designs and multimodal regimens. As the field strides toward clinical maturity, nanotechnology is poised to unlock the full potential of immunotherapy, paving the way for adaptive, immune-guided, and potentially curative cancer therapies.
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