Immunotherapy via PD-L1-presenting biomaterials leads to long-term islet graft survival.
Maria M CoronelKaren E MartinMichael D HuncklerGraham BarberEric B O'NeillJuan D MedinaEnrico OpriClaire A McClainLalit BatraJessica D WeaverHong Seo LimPeng QiuEdward A BotchweyEsma S YolcuHaval ShirwanAndres J GarciaPublished in: Science advances (2020)
Antibody-mediated immune checkpoint blockade is a transformative immunotherapy for cancer. These same mechanisms can be repurposed for the control of destructive alloreactive immune responses in the transplantation setting. Here, we implement a synthetic biomaterial platform for the local delivery of a chimeric streptavidin/programmed cell death-1 (SA-PD-L1) protein to direct "reprogramming" of local immune responses to transplanted pancreatic islets. Controlled presentation of SA-PD-L1 on the surface of poly(ethylene glycol) microgels improves local retention of the immunomodulatory agent over 3 weeks in vivo. Furthermore, local induction of allograft acceptance is achieved in a murine model of diabetes only when receiving the SA-PD-L1-presenting biomaterial in combination with a brief rapamycin treatment. Immune characterization revealed an increase in T regulatory and anergic cells after SA-PD-L1-microgel delivery, which was distinct from naïve and biomaterial alone microenvironments. Engineering the local microenvironment via biomaterial delivery of checkpoint proteins has the potential to advance cell-based therapies, avoiding the need for systemic chronic immunosuppression.
Keyphrases
- immune response
- cell therapy
- tissue engineering
- case report
- single cell
- induced apoptosis
- type diabetes
- stem cells
- cardiovascular disease
- dna damage
- papillary thyroid
- dendritic cells
- high throughput
- toll like receptor
- cell cycle arrest
- squamous cell carcinoma
- amino acid
- small molecule
- cell cycle
- inflammatory response
- mesenchymal stem cells
- squamous cell
- oxidative stress
- young adults
- endoplasmic reticulum stress
- combination therapy
- climate change
- bone marrow
- skeletal muscle
- childhood cancer
- replacement therapy