B cells play a more sinister role than believed in progression of type 1 diabetes

A recent study by Vanderbilt Health researchers has revealed a greater, detrimental role for B lymphocytes (B cells) in the progression of type 1 diabetes (T1D).

B cells are immune cells thought to drive the immune system’s attack on insulin-producing beta cells by activating anti-islet T cells. The study published in Diabetes suggests they play an even more sinister role by also interfering with and limiting the function of regulatory T cells (Tregs) that help calm the immune system.

“Our study showed B cells can weaken the body’s natural defenses by interfering with Tregs, which normally behave as peacekeepers to ward off immune attacks on the pancreas and the insulin-producing beta cells,” said Daniel Moore, MD, PhD, associate professor of Pediatrics at Vanderbilt Health and the study’s corresponding author.

“In mouse models that lacked B cells, Tregs were stronger and more effective, which allowed transplanted insulin-producing pancreatic tissue to survive longer.

“This finding shifts our understanding of B lymphocytes from serving as simple accomplices in the development of type 1 diabetes to more active saboteurs. By focusing on these interactions, we hope to advance the development of innovative strategies to better preserve beta cells, delay or prevent type 1 diabetes, and improve patient outcomes. We also believe this may be an important, unrecognized part of immune regulation that may be at work in other autoimmune disorders, so we hope this new insight becomes more widely investigated.”

The study used various mouse models to investigate the role of B cells in T1D. Flow cytometry, magnetic-activated cell sorting, and immunohistochemistry were used to analyze Treg populations and their functions.

The mouse models showed that lack of B cells enables durable islet transplant tolerance, enhances the expansion of Tregs, increases the ratio of insulin-reactive Tregs to activated or effector T cells, and enhances islet-protective Treg function.

These findings indicate that B lymphocytes accelerate destructive immunity by negatively regulating Treg development and function. The researchers note that targeting the B cell-Treg interactions, particularly in the thymus gland where T cells are produced, might offer new, more selective therapeutic strategies.