Answer:
Step-by-step explanation:
The host's immune response to the transplanted graft, which is commonly exhibited as pericapsular fibrotic overgrowth (PFO), is one of the key causes of defective encapsulated islets in (PFO).PFO creates a barrier upon this capsule surface that inhibits and impedes oxygen and nutrients from entering, resulting in islet cell deprivation, hypoxia, and/or death. This host immune response was missing under in vitro circumstances, which explains why glucose sensing and insulin release were more efficient than in vivo circumstances. Nonetheless, utilizing nanoporous encapsulation or modifying the microcapsular shape and geometry can solve these issues.