Abstract
B-cells participate in the autoimmune response that precedes the onset of type 1 diabetes, but how these cells contribute to disease progression is unclear. In this study, we analyzed the phenotype and functional characteristics of islet-infiltrating B-cells in the diabetes-prone NOD mouse and in the insulitis-prone but diabetes-resistant (NODxNOR)F1 mouse. The results indicate that B-cells accumulate in the islets of both mice influenced by sex traits. Phenotypically and functionally, these B-cells are highly affected by the islet inflammatory milieu, which may keep them in a silenced status. Moreover, although isletinfiltrating B-cells seem to be antigen experienced, they can only induce islet-infiltrating T-cell proliferation when they act as accessory cells. Thus, these results strongly suggest that islet-infiltrating B-cells do not activate isletinfiltrating T-cells in situ, although they may affect the progression of the disease otherwise. © 2007 by the American Diabetes Association.
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CITATION STYLE
Puertas, M. C., Carrillo, J., Pastor, X., Ampudia, R. M., Alba, A., Planas, R., … Verdaguer, J. (2007). Phenotype and functional characteristics of islet-infiltrating B-cells suggest the existence of immune regulatory mechanisms in islet milieu. Diabetes, 56(4), 940–949. https://doi.org/10.2337/db06-0428
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