Yersinia Pseudotuberculosis Modulates Regulatory T Cell Stability via Injection of Yersinia Outer Proteins in a Type III Secretion System-Dependent Manner.

European Journal of Microbiology & Immunology Pub Date : 2018-11-28 eCollection Date: 2018-12-23 DOI:10.1556/1886.2018.00015
Ahmed Elfiky, Agnes Bonifacius, Joern Pezoldt, Maria Pasztoi, Paweena Chaoprasid, Pooja Sadana, Nagla El-Sherbeeny, Magda Hagras, Andrea Scrima, Petra Dersch, Jochen Huehn
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引用次数: 5

Abstract

Adaptive immunity is essentially required to control acute infection with enteropathogenic Yersinia pseudotuberculosis (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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假结核耶尔森菌通过注射耶尔森菌外蛋白以III型分泌系统依赖的方式调节调节性T细胞的稳定性。
适应性免疫是控制肠致病性假结核耶尔森菌(Yptb)急性感染的必要条件。我们最近证明了Yptb可以直接调节naïve CD4+ T细胞分化。然而,完全分化的叉头盒蛋白P3 (Foxp3+)调节性T细胞(Tregs)作为维持免疫稳态的关键角色,是否被Yptb靶向仍然是未知的。在这里,我们证明了在CD4+ T细胞室内,Yptb优先靶向Tregs并在依赖于III型分泌系统和入侵的过程中注射耶尔森氏菌外蛋白(Yops)。值得注意的是,yop易位到离体分离的Foxp3+ Tregs中导致Foxp3表达显著下调,免疫抑制细胞因子白介素-10 (IL-10)表达能力下降。总之,这些发现强调了入侵蛋白是介导Yptb附着在Foxp3+ Tregs上的关键,这允许有效的yop易位,并最终实现Foxp3+ Tregs抑制表型的调节。
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