Nanoscale coordination polymers induce immunogenic cell death by amplifying radiation therapy mediated oxidative stress.
Zhusheng HuangYuxiang WangDan YaoJinhui WuYiqiao HuAhu YuanPublished in: Nature communications (2021)
Radiation therapy can potentially induce immunogenic cell death, thereby priming anti-tumor adaptive immune responses. However, radiation-induced systemic immune responses are very rare and insufficient to meet clinical needs. Here, we demonstrate a synergetic strategy for boosting radiation-induced immunogenic cell death by constructing gadolinium-hemin based nanoscale coordination polymers to simultaneously perform X-ray deposition and glutathione depletion. Subsequently, immunogenic cell death is induced by sensitized radiation to potentiate checkpoint blockade immunotherapies against primary and metastatic tumors. In conclusion, nanoscale coordination polymers-sensitized radiation therapy exhibits biocompatibility and therapeutic efficacy in preclinical cancer models, and has the potential for further application in cancer radio-immunotherapy.
Keyphrases
- radiation induced
- cell death
- radiation therapy
- immune response
- papillary thyroid
- cell cycle arrest
- oxidative stress
- atomic force microscopy
- squamous cell
- locally advanced
- dna damage
- small cell lung cancer
- squamous cell carcinoma
- dendritic cells
- toll like receptor
- high resolution
- cell cycle
- magnetic resonance
- rectal cancer
- climate change
- young adults
- mass spectrometry
- mesenchymal stem cells
- cell proliferation
- human health
- heat shock