Author/Authors :
Jacob Nattermann، نويسنده , , Angelika Maria Schneiders، نويسنده , , Ludger Leifeld، نويسنده , , Bettina Langhans، نويسنده , , Monika Schulz، نويسنده , , Geneviève Inchauspe، نويسنده , , Bertfried Matz، نويسنده , , Hans H. Brackmann، نويسنده , , Michael Houghton، نويسنده , , Tilman Sauerbruch، نويسنده , , Ulrich Spengler، نويسنده ,
Abstract :
Background/Aims
The role of antibody dependent cellular cytotoxicity (ADCC) in HCV infection is unclear at present. Antibodies mediating ADCC are usually directed against viral envelope proteins. As cell surface expression of the HCV envelope E2 protein has been shown, the HCV E2 protein is an especially promising candidate target for ADCC.
Methods
Sera from patients with acute (n=6), self-limited (n=11) and chronic (n=19) HCV infection were analyzed in this study. Sera reacting with cell-bound HCV antigens were examined in a flowcytometric cytotoxicity assay using antigen-coated JOK-1 cells as targets.
Results
We found that sera from all stages of HCV infection reacted with cells loaded with HCV E2. E2-specific ADCC was observed in patients with acute (n=3/6), self-limited (n=5/11) and chronic (n=13/19) hepatitis C and was closely related to fluorescence intensity in the E2-binding assay (r=0.67, P<0.001).
Conclusions
We conclude that E2-antibodies from all stages of HCV infection can mediate ADCC. Thus, the role of this process in the pathogenesis of chronic hepatitis C should be further elucidated.