New research reveals that in very young children diagnosed with type 1 diabetes (T1D), nearly all insulin-producing beta cells in the pancreas are destroyed before reaching full maturity. This early destruction helps explain why the disease progresses more rapidly and severely in this age group compared to adolescents and adults.
Scientists from multiple international research centers examined pancreatic tissue and immune activity in young children with T1D. They discovered a clear pattern: beta cells in children under seven tend to be less mature and more susceptible to immune attack. In contrast, older children and adults retain a greater number of partially functional cells at diagnosis.
The study suggests that the immature beta cells of young children may express distinct molecular markers, making them easier targets for the immune system. Researchers believe this insight could guide the development of future therapies aimed at protecting or restoring insulin-producing cells more effectively in young patients.
These findings may help refine age-specific treatment approaches. Interventions that focus on preserving immature beta cells or promoting their maturation could potentially slow disease progression in young children. This could also support more personalized strategies for preventing or delaying the onset of type 1 diabetes.
Researchers also noted differences in genetic and immunological responses between younger and older patients. Some genes related to immune regulation appear to be more active in younger children, possibly intensifying the autoimmune reaction.
“Understanding how the age of onset affects the biology of type 1 diabetes is key to designing better interventions,” said one of the lead investigators.
“The immune system seems to attack pancreatic cells more aggressively in children whose cells are still developing.”
Building on these findings, scientists are exploring whether early interventions could modify the immune response or enhance the resilience of beta cells in high-risk children. Clinical trials targeting immune modulation in early childhood may soon follow.
Author’s summary:
The study shows that immature pancreatic beta cells in very young children make type 1 diabetes more aggressive, offering new avenues for therapies to protect developing cells.