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The GOR gene product cannot cross-react with hepatitis C virus in humans
R Koike1, T Iizuka, T Watanabe
1First Department of Internal Medicine, Tokyo Medical and Dental University, Japan. kryu.rheu@tmd.ac.jp
Clinical and Experimental Immunology
|July 27, 2001
Summary
The GOR47--1 epitope, initially thought to cross-react with hepatitis C virus (HCV), is not translated in humans. This finding suggests limited connection between the GOR gene product and autoimmune phenomena in humans.
Area of Science:
- Immunology
- Virology
- Genetics
Background:
- The GOR47--1 epitope, a host-derived antigen, was identified for its cross-reactivity with hepatitis C virus (HCV).
- Its potential role in autoimmune phenomena associated with HCV infection and autoimmune hepatitis remains controversial.
- Enzyme immunosorbent assays (ELISA) using GOR47--1 show promise for HCV screening.
Purpose of the Study:
- To investigate the translation of the GOR47--1 epitope in humans.
- To explore the correlation between antibodies to GOR epitopes and autoimmune phenomena in HCV patients.
- To clarify the relationship between the GOR gene product and autoimmunity in humans.
Main Methods:
- Isolation of the human GOR gene.
- Analysis of GOR epitope translation in humans via genetic sequencing.
- Detection of antibodies against GOR epitopes (GOR47--1 and GOR1--125) in patient sera.
- Correlation analysis between antibody presence, autoimmune markers, and serum IgG levels.
Main Results:
- The GOR47--1 epitope is not translated in humans due to a single base substitution compared to chimpanzees.
- Antibodies against the translatable human GOR1--125 epitope were found in some patients.
- No correlation was observed between anti-GOR47--1 or anti-GOR1--125 antibodies and autoimmune phenomena.
- Serum IgG levels did not affect the titers of these antibodies.
Conclusions:
- The non-translation of the GOR47--1 epitope in humans suggests a minimal relationship between the GOR gene product and human autoimmunity.
- Further investigation into the cross-reactivity mechanisms between HCV and the GOR gene product is warranted.