A nanoscale innate immune multiplier amplifies immunogenic cell death triggered by oxaliplatin via enhancing systemic and trained immunity

先天免疫系统 奥沙利铂 免疫系统 免疫 免疫学 医学 癌症 内科学 结直肠癌
作者
Yang Zhang,Zhicheng Yan,Shuo Geng,Yueheng Wang,Junji Ren,Yunhui Jiang,Liuqing Yang,Wenbing Dai,Hua Zhang,Xueqing Wang,Nan Zheng,Qiang Zhang,Bing He
出处
期刊:Nano Today [Elsevier BV]
卷期号:65: 102835-102835 被引量:2
标识
DOI:10.1016/j.nantod.2025.102835
摘要

Inducing immunogenic cell death (ICD) of cancer cells is the key for cytotoxic drugs to improve the synergy with immunotherapy. However, due to the immunosuppressive microenvironment and the cytotoxicity differences of drugs, ICD effects are often insufficient and difficult to effectively and durably activate anti-tumor immune responses. Here, we performed a network meta-analysis (NMA) based on clinical data of gastrointestinal cancer and identified oxaliplatin (Oxp) as an effective ICD-inducing drug. Meanwhile, to overcome the negative effects of immunosuppressive microenvironment on ICD, we constructed a nanoscale innate immune multiplier (NIIM) composed of nano-granulated manganous zoledronate, and designed a systemic delivery strategy to achieve the superposition of innate immune responses from multiple sites and amplify the ICD effect of Oxp. NIIM was first targeted to the tumor tissue, where it concurrently engaged tumor cells and innate immunocytes to reverse the immunosuppressive microenvironment. Following intravenous administration, NIIM was also distributed to the spleen, where it activated Ly6C + inflammatory monocytes, directly augmenting the phagocytosis and elimination of tumor cells, and inducing the tumor-killing efficacy by cytotoxic T cells. Additionally, NIIM modulated the composition of hematopoietic progenitor cells in the bone marrow, inducing a durable innate immune response through trained immunity. The superposition of these immune effects allowed NIIM to significantly enhance the efficacy of oxaliplatin in gastrointestinal cancers after only one single injection. In summary, this strategy of simultaneously activating intratumoral, systemic, and trained immunity based on intravenous NIIM provides an effective new approach to amplify ICD of cytotoxic drugs and achieve the efficient synergy of chemotherapy with immunotherapy. • Oxaliplatin exhibits more potent ICD-inducing capacity than cisplatin in gastrointestinal cancer based on clinical data. • A nanoscale innate immune multiplier (NIIM) composing Zole and Mn 2+ is designed to amplify the ICD effect of oxaliplatin. • Intravenous NIIM acts like a signal amplifier to achieve the superposition of innate immune effects from multiple sites. • Intravenous NIIM simultaneously activated intratumoral, systemic, and trained immunity. • NIIM significantly enhanced the efficacy of oxaliplatin in gastrointestinal cancers after only one single injection.
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