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PDCD1 and IFNL4 genetic variants and risk of developing hepatitis C virus-related diseases.

Valli De ReMaria Lina TorneselloMariangela De ZorziLaura CaggiariFrancesca PezzutoPatrizia LeoneVito RacanelliGianfranco LaulettaStefania ZanussiOmbretta RepettoLaura GragnaniFrancesca Maria RossiRiccardo DolcettiAnna Linda ZignegoFranco Maria BuonaguroAgostino Steffan
Published in: Liver international : official journal of the International Association for the Study of the Liver (2021)
Studies of IFNL4 and PDCD1 genes are helpful to better understand the role of host genetic factors and immune antigens influencing the outcome of HCV-related diseases. Our data support an association between the expression of IFNλ4, which prevents the expression of IFNλ3, with all the different HCV-related diseases studied, and besides, evidence that a higher IFNλ4 expression is associated with hepatocellular at a younger age. The expression pattern of low PD-L1 on B cells and high PD-1 on CD4+T-cells in patients with HCV-positive cryoglobulinaemia suggests a critical role of the PD-1/PD-L1 signaling in modulating B cell-T cell interaction in this lymphoproliferative disease.
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