TY - JOUR
T1 - Imaging of hepatitis C virus infection in liver grafts after liver transplantation
AU - Mensa, Laura
AU - Pérez-Del-Pulgar, Sofía
AU - Crespo, Gonzalo
AU - Koutsoudakis, George
AU - Fernández-Carrillo, Carlos
AU - Coto-Llerena, Mairene
AU - Miquel, Rosa
AU - Allende, Helena
AU - Castells, Lluís
AU - Navasa, Miquel
AU - Forns, Xavier
PY - 2013/8/1
Y1 - 2013/8/1
N2 - Background & Aims The detection of native hepatitis C virus (HCV) antigens in liver tissue may be relevant to diagnostic purposes and to better understand the pathogenesis of HCV infection. The aim of our study was to characterize HCV antigens in liver grafts. Methods We selected 32 liver transplant (LT) recipients with recurrent hepatitis C. HCV core and NS5A antigens were detected in formalin-fixed, paraffin-embedded (FFPE) liver biopsies obtained immediately after graft reperfusion (negative controls), during the acute phase of HCV infection (1-6 months) and during follow-up (7-74 months) after LT. Viral antigens were assessed by immunohistochemistry and confocal microscopy. Results All reperfusion biopsies were negative for both antigens. Core protein was detected in 75% and 33% of acute phase and follow-up biopsies, respectively. HCV antigens were not detected in any of the 10 samples from patients who cleared HCV after antiviral treatment. Immunostaining was hepatocellular, with a granular cytoplasmic pattern and a wide spectrum of intensity. We found a significant association between viral load and the presence of HCV core-positive hepatocytes (p = 0.004). NS5A colocalized strongly with core (66%) and adipophilin (36%), supporting the localization of core and NS5A around lipid droplets. A detailed three-dimensional analysis showed that NS5A surrounded the core and adipophilin-positive areas. Conclusions HCV antigens can be detected in FFPE liver biopsies by immunohistochemistry. The in vivo colocalization of core and NS5A proteins around the lipid droplets supports that the latter may play a role in virus particle production, similar to what reported in vitro. © 2013 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
AB - Background & Aims The detection of native hepatitis C virus (HCV) antigens in liver tissue may be relevant to diagnostic purposes and to better understand the pathogenesis of HCV infection. The aim of our study was to characterize HCV antigens in liver grafts. Methods We selected 32 liver transplant (LT) recipients with recurrent hepatitis C. HCV core and NS5A antigens were detected in formalin-fixed, paraffin-embedded (FFPE) liver biopsies obtained immediately after graft reperfusion (negative controls), during the acute phase of HCV infection (1-6 months) and during follow-up (7-74 months) after LT. Viral antigens were assessed by immunohistochemistry and confocal microscopy. Results All reperfusion biopsies were negative for both antigens. Core protein was detected in 75% and 33% of acute phase and follow-up biopsies, respectively. HCV antigens were not detected in any of the 10 samples from patients who cleared HCV after antiviral treatment. Immunostaining was hepatocellular, with a granular cytoplasmic pattern and a wide spectrum of intensity. We found a significant association between viral load and the presence of HCV core-positive hepatocytes (p = 0.004). NS5A colocalized strongly with core (66%) and adipophilin (36%), supporting the localization of core and NS5A around lipid droplets. A detailed three-dimensional analysis showed that NS5A surrounded the core and adipophilin-positive areas. Conclusions HCV antigens can be detected in FFPE liver biopsies by immunohistochemistry. The in vivo colocalization of core and NS5A proteins around the lipid droplets supports that the latter may play a role in virus particle production, similar to what reported in vitro. © 2013 European Association for the Study of the Liver. Published by Elsevier B.V. All rights reserved.
KW - Confocal microscopy
KW - HCV antigen detection
KW - Hepatitis C virus
KW - Liver transplantation
U2 - 10.1016/j.jhep.2013.03.023
DO - 10.1016/j.jhep.2013.03.023
M3 - Article
SN - 0168-8278
VL - 59
SP - 271
EP - 278
JO - Journal of Hepatology
JF - Journal of Hepatology
IS - 2
ER -