Promotion of triple negative breast cancer immunotherapy by combining bioactive radicals with immune checkpoint blockade

被引:2
作者
Chen, Meixu [1 ,2 ]
Song, Linlin [1 ,2 ,3 ,4 ]
Zhou, Yao [1 ,2 ]
Xu, Tianyue [1 ,2 ]
Sun, Ting [1 ,2 ,5 ]
Liu, Zhihui [1 ,2 ]
Xu, Zihan [1 ,2 ]
Zhao, Yujie [1 ,2 ]
Du, Peixin [1 ,2 ]
Ma, Yingying [1 ,2 ]
Huang, Liwen [1 ,2 ]
Chen, Xiaoting [6 ]
Yang, Guang [6 ]
Jing, Jing [1 ,2 ]
Shi, Hubing [1 ,2 ]
机构
[1] Sichuan Univ, West China Hosp, Inst Breast Hlth Med, State Key Lab Biotherapy, Chengdu 610041, Sichuan, Peoples R China
[2] Collaborat Innovat Ctr, Chengdu 610041, Sichuan, Peoples R China
[3] Sichuan Univ, West China Hosp, Dept Ultrasound, Chengdu 610041, Sichuan, Peoples R China
[4] Sichuan Univ, West China Hosp, Lab Ultrasound Med, Chengdu 610041, Sichuan, Peoples R China
[5] Sichuan Univ, West China Hosp, Dept Crit Care Med, Chengdu 610041, Sichuan, Peoples R China
[6] Sichuan Univ, West China Hosp, Anim Expt Ctr, Chengdu 610041, Peoples R China
基金
中国国家自然科学基金;
关键词
Ozone; Reactive nitrogen species; Immune checkpoint blockade; Controlled-release system; Triple-negative breast cancer; RRX-001; CD47; PEROXYNITRITE; MACROPHAGES; COMBINATION; CELLS; MYC;
D O I
10.1016/j.actbio.2025.01.015
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Although immunotherapy has revolutionized clinical cancer treatment, the efficacy is limited due to the lack of tumor-associated antigens (TAAs) and the presence of compensatory immune checkpoints. To overcome the deficiency, a nano-system loaded with ozone and CD47 inhibitor RRx-001 is designed and synthesized. Upon irradiation, reactive oxygen species (ROS) generated from ozone reacts with nitric oxide (NO) metabolized from RRx-001 to form reactive nitrogen species (RNS), which presents a much stronger cell-killing ability than ROS. Molecular mechanism studies further reveal that RNS induce extensive immunogenic cell death (ICD). The released TAAs promote infiltration of cytotoxic T lymphocytes, which provides the basis for immune checkpoint blockade (ICB) therapy. Meanwhile, RRx-001 carried by the nanoparticles and the produced radicals repolarize M2-type tumor-associated macrophages (TAMs) into the anti-tumor M1-type, consequently reversing the immunosuppressive tumor microenvironment (TME). In a xenograft triple-negative breast cancer (TNBC) animal model, O3-001@lipo (liposome enwrapping O3 and RRx-001) plus irradiation shows a significant anti-tumor efficacy by improving cytotoxic lymphocyte infiltration and regulating immunosuppressive TME. In summary, the O3-001@lipo nano-system triggered by irradiation potently improves the efficacy of immunotherapy by introducing strong cytotoxic RNS, which not only enriches the toolbox of ICD inducer but also provides a strategy of treatment for immune deficient tumor. Statement of significance: This study introduces a nano-system that leverages ozone and RRx-001 in the presence of X-ray irradiation to generate reactive nitrogen species, enhancing immunogenic cell death and promoting Tlymphocyte infiltration in triple-negative breast cancer, addressing a significant unmet need in the field. The scientific contribution is the development of a clinically translatable nano-system that not only induces ICD but also reshapes the tumor microenvironment, which is expected to have a profound impact on the readership in pharmaceutics, material science, and nano-bio interaction, particularly for those interested in advanced immune therapy approaches.
引用
收藏
页码:305 / 322
页数:18
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