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Updated: Aug 9, 2026

Anti-Nuclear Antibody Screening Using HEp-2 Cells
Published on: June 24, 2014
Antibodies to nuclear lamin C in chronic hepatitis delta virus infection
J Wesierska-Gadek1, E Penner, E Hitchman
1Institute of Tumorbiology-Cancer Research, University of Vienna, Austria.
Insights
Researchers identified a novel autoantibody in chronic hepatitis delta virus infection that targets nuclear lamin C. This finding advances understanding of autoimmune responses in liver disease.
Area of Science:
- Immunology
- Hepatology
- Cell Biology
Background:
- Chronic hepatitis delta virus (HDV) infection is a significant cause of liver disease.
- Autoantibodies are common in chronic liver diseases, but their specific targets in HDV infection are not fully characterized.
Purpose of the Study:
- To identify the specific nuclear antigen targeted by autoantibodies in patients with chronic HDV infection.
- To characterize the reactivity of these autoantibodies against different nuclear components.
Main Methods:
- Indirect immunofluorescence was used to detect antibody binding in patient sera.
- Immunoblotting experiments utilized isolated nuclei, nuclear matrices, nuclear pore complex-lamina fractions, and purified lamins A and C as antigens.
- Reactivity patterns were analyzed to pinpoint the specific autoantigen.
Main Results:
- Sera from patients with chronic HDV infection showed staining at the nuclear periphery.
- Nuclear lamin C was identified as the primary reactive antigen in 8 out of 10 tested sera.
- The autoantibodies predominantly recognized nuclear lamin C exclusively, not nuclear lamins A or B.
Conclusions:
- A novel autoantibody associated with chronic HDV infection specifically targets nuclear lamin C.
- The autoantibody likely recognizes an epitope within the carboxyterminal region of nuclear lamin C.
- This discovery contributes to understanding the immunopathogenesis of HDV infection and related autoimmune responses.
Abstract:
Sera of patients with chronic hepatitis delta virus infection stained the nuclear periphery in indirect immunofluorescence. Using proteins of isolated nuclei, isolated nuclear matrices, the nuclear pore complex-lamina fraction and purified lamins A and C as antigen source in immunoblotting experiments, nuclear lamin C was identified as the reactive antigen. Most sera tested (8 of 10) recognized nuclear lamin C exclusively, but not the nuclear lamins A and B. Antibodies reacting with both nuclear lamins A and C, which share extensive sequence homologies, have been reported to occur in autoimmune hepatitis and primary biliary cirrhosis. The present findings suggest that the novel autoantibody associated with chronic hepatitis delta virus infection recognizes an epitope localized in the short carboxyterminal region of nuclear lamin C.
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