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Article Abstract

Adaptive immunity is essentially required to control acute infection with enteropathogenic (Yptb). We have recently demonstrated that Yptb can directly modulate naïve CD4 T cell differentiation. However, whether fully differentiated forkhead box protein P3 (Foxp3) regulatory T cells (Tregs), fundamental key players to maintain immune homeostasis, are targeted by Yptb remains elusive. Here, we demonstrate that within the CD4 T cell compartment Yptb preferentially targets Tregs and injects Yersinia outer proteins (Yops) in a process that depends on the type III secretion system and invasins. Remarkably, Yop-translocation into ex vivo isolated Foxp3 Tregs resulted in a substantial downregulation of Foxp3 expression and a decreased capacity to express the immunosuppressive cytokine interleukin-10 (IL-10). Together, these findings highlight that invasins are critically required to mediate Yptb attachment to Foxp3 Tregs, which allows efficient Yop-translocation and finally enables the modulation of the Foxp3 Tregs' suppressive phenotype.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6348704PMC
http://dx.doi.org/10.1556/1886.2018.00015DOI Listing

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