Inhibition of post-surgery tumour recurrence via a hydrogel releasing CAR-T cells and anti-PDL1-conjugated platelets.
Quanyin HuHongjun LiEdikan A OgunnaikeQian ChenHuitong RuanSarah AhnElena DukhovlinovaYang KangDi WenGianpietro DottiZhen GuPublished in: Nature biomedical engineering (2021)
The immunosuppressive microenvironment of solid tumours reduces the antitumour activity of chimeric antigen receptor T cells (CAR-T cells). Here, we show that the release-through the implantation of a hyaluronic acid hydrogel-of CAR-T cells targeting the human chondroitin sulfate proteoglycan 4, polymer nanoparticles encapsulating the cytokine interleukin-15 and platelets conjugated with the checkpoint inhibitor programmed death-ligand 1 into the tumour cavity of mice with a resected subcutaneous melanoma tumour inhibits the local recurrence of the tumour as well as the growth of distant tumours, through the abscopal effect. The hydrogel, which functions as a reservoir, facilitates the enhanced distribution of the CAR-T cells within the surgical bed, and the inflammatory microenvironment triggers platelet activation and the subsequent release of platelet-derived microparticles. The post-surgery local delivery of combination immunotherapy through a biocompatible hydrogel reservoir could represent a translational route for preventing the recurrence of cancers with resectable tumours.
Keyphrases
- hyaluronic acid
- minimally invasive
- coronary artery bypass
- drug delivery
- stem cells
- free survival
- lymph node
- induced apoptosis
- endothelial cells
- dna damage
- photodynamic therapy
- surgical site infection
- wound healing
- tissue engineering
- cell proliferation
- cancer therapy
- coronary artery disease
- squamous cell carcinoma
- signaling pathway
- ionic liquid
- atrial fibrillation
- induced pluripotent stem cells
- drug release
- water quality
- liver metastases