Immunostimulant hydrogel for the inhibition of malignant glioma relapse post-resection.
Jing ZhangChen ChenAnning LiWeiqiang JingPeng SunXueyang HuangYingchao LiuShengchang ZhangWei DuRui ZhangYing LiuAihua GongJibiao WuXinyi JiangPublished in: Nature nanotechnology (2021)
Immunotherapies have revolutionized intervention strategies for many primary cancers, but have not improved the outcomes of glioblastoma multiforme (GBM), which remains one of the most lethal malignant cerebral tumours. Here we present an injectable hydrogel system that stimulates tumoricidal immunity after GBM surgical resection, which mitigates its relapse. The hydrogel comprises a tumour-homing immune nanoregulator, which induces immunogenic cell death and suppression of indoleamine 2,3-dioxygenase-1, and chemotactic CXC chemokine ligand 10, for a sustained T-cell infiltration. When delivered in the resected tumour cavity, the hydrogel system mimics a 'hot' tumour-immunity niche for attacking residual tumour cells and significantly suppresses postoperative GBM recurrence. Our work provides an alternative strategy for conferring effective tumoricidal immunity in GBM patients, which may have a broad impact in the immunotherapy of 'cold' tumours after surgical intervention.
Keyphrases
- hyaluronic acid
- drug delivery
- tissue engineering
- cell death
- randomized controlled trial
- wound healing
- end stage renal disease
- free survival
- cell cycle arrest
- prognostic factors
- ejection fraction
- induced apoptosis
- chronic kidney disease
- lymph node
- signaling pathway
- peritoneal dialysis
- young adults
- skeletal muscle
- patient reported outcomes
- cell proliferation
- blood brain barrier
- cerebral ischemia
- pi k akt