Light triggered release of a triple action porphyrin-cisplatin conjugate evokes stronger immunogenic cell death for chemotherapy, photodynamic therapy and cancer immunotherapy

被引:0
作者
Haiqin Song
Zhenghao Cai
Juyi Li
Haihua Xiao
Ruogu Qi
Minhua Zheng
机构
[1] Ruijin Hospital,Department of General Surgery, School of Medicine
[2] Shanghai Jiaotong University,Department of Materials Science and Chemical Engineering
[3] Stony Brook University,Beijing National Laboratory for Molecular Sciences, State Key Laboratory of Polymer Physics and Chemistry, Institute of Chemistry
[4] Chinese Academy of Sciences,School of Medicine and Holistic Integrative Medicine
[5] Nanjing University of Chinese Medicine,undefined
来源
Journal of Nanobiotechnology | / 20卷
关键词
Porphyrin; Cisplatin; Immunogenic cell death; Cancer immunotherapy; Photodynamic therapy; Nanoparticles;
D O I
暂无
中图分类号
学科分类号
摘要
Photodynamic therapy (PDT) has emerged as an attractive therapeutic approach which can elicit immunogenic cell death (ICD). However, current ICD inducers are still very limited as the representative ICD induces of photosensitizers can only evoke insufficient ICD to achieve unsatisfactory cancer immunotherapy. Herein, we demonstrated the use of a triple action cationic porphyrin-cisplatin conjugate (Pt-1) for drug delivery by a reactive oxygen species (ROS) sensitive polymer as nanoparticles (NP@Pt-1) for combined chemotherapy, PDT and immunotherapy. This unique triple action Pt-1 contains both chemotherapeutic Pt drugs and Porphyrin as a photosensitizer to generate ROS for PDT. Moreover, the ROS generated by Pt-1 can on the one hand degrade polymer carriers to release Pt-1 for chemotherapy and PDT. On the other hand, the ROS generated by Pt-1 subsequently triggered the ICD cascade for immunotherapy. Taken together, we demonstrated that NP@Pt-1 were the most effective and worked in a triple way. This study could provide us with new insight into the development of nanomedicine for chemotherapy, PDT as well as cancer immunotherapy.
引用
收藏
相关论文
共 72 条
  • [1] Galluzzi L(2021)Consensus guidelines for the definition, detection and interpretation of immunogenic cell death J Immunother Cancer. 8 262-275
  • [2] Yatim N(2017)Dying cells actively regulate adaptive immune responses Nat Rev Immunol 4 4854-4865
  • [3] Cullen S(2019)Immunogenic cell death in cancer therapy: present and emerging inducers J Cell Mol Med 23 53-71
  • [4] Albert ML(2010)Immunogenic cell death, DAMPs and anticancer therapeutics: an emerging amalgamation Biochim Biophys Acta. 1805 860-875
  • [5] Zhou J(2012)Immunogenic cell death and DAMPs in cancer therapy Nat Rev Cancer 12 278-291
  • [6] Wang G(2017)TLR-induced murine dendritic cell (DC) activation requires DC-intrinsic complement J Immunol 199 1293-1308.e36
  • [7] Chen Y(2018)Single-cell map of diverse immune phenotypes in the breast tumor microenvironment Cell 174 5241-5259
  • [8] Wang H(2021)Therapy-induced tumor cell death: friend or foe of immunotherapy? Front Oncol 11 1292-1307
  • [9] Hua Y(2020)Prodrug-based versatile nanomedicine for enhancing cancer immunotherapy by increasing immunogenic cell death Small 16 1923-1937
  • [10] Cai Z(2019)Nanomedicine-based immunotherapy for the treatment of cancer metastasis Adv Mater 31 98-104