Type 1 diabetes (T1D) is characterized by insulin deficiency resulting from the selective destruction of pancreatic β-cells by self-reactive T cells. Recent evidence demonstrates that innate immune responses substan-tially contribute to the pathogenesis of T1D, as they represent a first line of response to danger/damage signals. Here we discuss evidenceonhow,inarelapsing-remitting pattern, pancreas remodeling, diet, micro-biota, gut permeability, and viral/bacterial infections induce the accumulation of leukocytes of the innate arm of the immune system throughout the pancreas. The subsequent acquisition and presentation of endocrine and exocrine antigens to the adaptive arm of the immune system results in a chronic progression of pancreatic damage. This process provides for the genera-tion of self-reactive T-cell responses; however, the relative weight that genetic and environmental factors have on the etiopathogenesis of T1D is endotype imprinted and patient specific. With this Perspectives in Diabetes, our goal is to encourage the scientific com-munity to rethink mechanisms underlying T1D pathogen-esis and to consider therapeutic approaches that focus on these processes in intervention trials within new-onset disease as well as in efforts seeking the disorder’s prevention in individuals at high risk.
CITATION STYLE
Petrelli, A., Atkinson, M. A., Pietropaolo, M., & Giannoukakis, N. (2021). Modulation of leukocytes of the innate arm of the immune system as a potential approach to prevent the onset and progression of type 1 diabetes. Diabetes, 70(2), 313–322. https://doi.org/10.2337/dbi20-0026
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