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10.1007/s12274-021-3432-x [DOI] [Google Scholar] Zhao Z., Song X., Zhang Y., Zeng B., Wu H., Guo S

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Activation of TIGIT signaling through agonists has been shown to suppress Th17 cell infiltration and attenuate inflammation, suggesting that TIGIT+ Tregs contribute to the resolution of immune-mediated tissue damage ( PD-1+ and TIGIT+ Tregs migrate to sites of inflammation in a chemokine receptor-dependent manner, with CCR6 and CCR7 playing pivotal roles in their tissue homing

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Since specific mediators driving changes in dysfunctional CD8 + T cell subsets in cirrhosis need further investigation, and their clinical relevance is yet to be fully understood, current immunotherapy strategies for cirrhosis predominantly target cells other than CD8 + T cells, such as macrophages