Abstract
Dendritic cells (DC) play a critical role in both the expansion of natural regulatory T cells (nTreg) and conversion of induced Treg (iTreg) from their precursors. In the present study, we evaluated the potential of DC to generate Treg from total CD4+ population which contains both nTreg and the precursors, and found that allogeneic (allo-DC) but not syngeneic DC (syn-DC) could effectively generated Foxp3+ Treg from total CD4+ population in the absence of exogenous cytokines. Compared with freshly purified CD4+ T cells, allo-DC-stimulated CD4+ T cells showed increased percentage of CD4+CD25+Foxp3+ Treg by 5-7-folds while syn-DC-stimulated CD4+ T cells did not. Furthermore, we demonstrated that the significant amounts of endogenous IL-2 and TGF-β, at least partially, contributed to the expansion of nTreg and conversion of iTreg in this cocultural system, respectively. Importantly, similar to nTreg, these allo-DC-generated Treg were capable of suppressing T cell response in vitro. Thus, our research provides a novel and efficient strategy for generation of Treg from total CD4+ population. © 2010 Blackwell Publishing Ltd.
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CITATION STYLE
Liu, C., Wang, Q., Liu, F., Li, H., Zhu, F., Wang, X., … Zhang, L. (2009). The allogeneic but not syngeneic dendritic cells effectively generated regulatory T cells from total Cd4+ population without exogenous cytokines. Scandinavian Journal of Immunology, 71(1), 12–19. https://doi.org/10.1111/j.1365-3083.2009.02334.x
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