AI Article Synopsis

  • Regulatory T cells (Tregs) help the body stay calm and not attack itself. They could be great for helping with organ transplants and autoimmune diseases, where the body gets confused and attacks its own cells.
  • Right now, people getting organ transplants usually have to take medicines forever to stop their bodies from rejecting the new organ, and there isn't a real cure for autoimmune diseases yet.
  • Scientists are figuring out how to make Treg therapy better by helping these cells go to the right places in the body and work longer, and using special materials could make this treatment even more effective.

Article Abstract

Regulatory T cells (Tregs) are crucial for preserving tolerance in the body, rendering Treg immunotherapy a promising treatment option for both organ transplants and autoimmune diseases. Presently, organ transplant recipients must undergo lifelong immunosuppression to prevent allograft rejection, while autoimmune disorders lack definitive cures. In the last years, there has been notable advancement in comprehending the biology of both antigen-specific and polyclonal Tregs. Clinical trials involving Tregs have demonstrated their safety and effectiveness. To maximize the efficacy of Treg immunotherapy, it is essential for these cells to migrate to specific target tissues, maintain stability within local organs, bolster their suppressive capabilities, and ensure their intended function's longevity. In pursuit of these goals, the utilization of biomaterials emerges as an attractive supportive strategy for Treg immunotherapy in addressing these challenges. As a result, the prospect of employing biomaterial-enhanced Treg immunotherapy holds tremendous promise as a treatment option for organ transplant recipients and individuals grappling with autoimmune diseases in the near future. This paper introduces strategies based on biomaterial-assisted Treg immunotherapy to enhance transplant medicine and autoimmune treatments.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11061617PMC
http://dx.doi.org/10.1016/j.bioactmat.2024.03.030DOI Listing

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