IMPROVED FUNCTIONALITY OF EXHAUSTED INTRAHEPATIC CXCR5+ CD8+ T CELLS CONTRIBUTES TO CHRONIC ANTIGEN CLEARANCE UPON IMMUNOMODULATION

Improved Functionality of Exhausted Intrahepatic CXCR5+ CD8+ T Cells Contributes to Chronic Antigen Clearance Upon Immunomodulation

Improved Functionality of Exhausted Intrahepatic CXCR5+ CD8+ T Cells Contributes to Chronic Antigen Clearance Upon Immunomodulation

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Chronic hepatotropic viral infections are characterized by exhausted CD8+ T cells in the presence of cognate antigen in the liver.The impairment of T cell response limits the control of chronic hepatotropic viruses.Immune-modulatory strategies are attractive options to re-invigorate exhausted T cells.However, in hepatotropic viral infections, the knowledge about immune-modulatory effects on the in-situ regulation of exhausted intrahepatic CD8+ T cells is limited.

In this study, we elucidated the functional heterogeneity in the pool of exhausted CD8+ T cells in the liver of mice expressing the model antigen Ova in a fraction of Political Communication Experiences of Sundanese Muslim Women Politicians hepatocytes.We found a subpopulation of intrahepatic CXCR5+ Ova-specific CD8+ T cells, which are profoundly cytotoxic, exhibiting efficient metabolic functions as well as improved memory recall and self-maintenance.The intrahepatic Ova-specific CXCR5+ CD8+ T cells are possibly tissue resident Improvement the estimation of reference evapotranspiration by combining different types of meteorological data Using machine learning models cells, which may rely largely on OXPHOS and glycolysis to fuel their cellular processes.Importantly, host conditioning with CpG oligonucleotide reinvigorates and promotes exhausted T cell expansion, facilitating complete antigen eradication.

The CpG oligonucleotide-mediated reinvigoration may support resident memory T cell formation and the maintenance of CXCR5+ Ova-specific CD8+ T cells in the liver.These findings suggest that CpG oligodinucleotide may preferentially target CXCR5+ CD8+ T cells for expansion to facilitate the revival of exhausted T cells.Thus, therapeutic strategies aiming to expand CXCR5+ CD8+ T cells might provide a novel approach against chronic liver infection.

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