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Comment
. 2017 Dec;14(12):954-956.
doi: 10.1038/cmi.2017.89. Epub 2017 Sep 11.

miR-31: a key player in CD8 T-cell exhaustion

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Comment

miR-31: a key player in CD8 T-cell exhaustion

Siddheshvar Bhela et al. Cell Mol Immunol. 2017 Dec.
No abstract available

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Conflict of interest statement

The authors declare no conflict of interest.

Figures

Figure 1
Figure 1
Model illustrating the role of miR-31 in CD8 T-cell biology during chronic viral infections. TCR and CD28 co-stimulation induces the upregulation of miR-31 in CD8 T cells. miR-31 promotes type 1 interferon signaling by targeting Ppp6C, a phosphatase that is a negative regulator of interferon signaling. Increased interferon signaling results in the increased expression of exhaustion genes and the decreased expression of effector genes, thus inducing an exhaustion phenotype. When miR-31 is knocked out in CD8 T cells, increased expression of Ppp6C reduces type 1 interferon and thus increases effector functionality.

Comment on

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