Dendritic Cells and Their Immunotherapeutic Potential for Treating Type 1 Diabetes.

Int J Mol Sci

Department of Pediatrics, Immunology Division, Faculty of Medicine and Health Sciences, Centre de Recherche du CHUS, Université de Sherbrooke, 3001, 12th Avenue North, Sherbrooke, QC J1H 5N4, Canada.

Published: April 2022

AI Article Synopsis

  • Type 1 diabetes (T1D) is caused by the destruction of pancreatic beta cells primarily by T cells, with dendritic cells (DCs) playing a key role in disease initiation and progression.
  • Recent research highlights the function of DCs as antigen-presenting cells that influence T cell responses by integrating signals from tissue damage and presenting antigens to naïve T cells.
  • Current therapeutic strategies aim to suppress the pro-inflammatory actions of DCs and enhance their ability to promote immune tolerance, focusing on both blocking T cell activation and promoting regulatory T cell populations to combat T1D.

Article Abstract

Type 1 diabetes (T1D) results from the destruction of pancreatic beta cells through a process that is primarily mediated by T cells. Emerging evidence suggests that dendritic cells (DCs) play a crucial role in initiating and developing this debilitating disease. DCs are professional antigen-presenting cells with the ability to integrate signals arising from tissue infection or injury that present processed antigens from these sites to naïve T cells in secondary lymphoid organs, thereby triggering naïve T cells to differentiate and modulate adaptive immune responses. Recent advancements in our knowledge of the various subsets of DCs and their cellular structures and methods of orchestration over time have resulted in a better understanding of how the T cell response is shaped. DCs employ various arsenal to maintain their tolerance, including the induction of effector T cell deletion or unresponsiveness and the generation and expansion of regulatory T cell populations. Therapies that suppress the immunogenic effects of dendritic cells by blocking T cell costimulatory pathways and proinflammatory cytokine production are currently being sought. Moreover, new strategies are being developed that can regulate DC differentiation and development and harness the tolerogenic capacity of these cells. Here, in this report, we focus on recent advances in the field of DC immunology and evaluate the prospects of DC-based therapeutic strategies to treat T1D.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC9099521PMC
http://dx.doi.org/10.3390/ijms23094885DOI Listing

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