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Up-regulation of RIP1 and IPS-1 in chronic HBV infected patients
Minoo Safari-Arababadi1, Mohammad Hossein Modarressi1,2, Mohammad Kazemi Arababadi3,4
1Department of Genetics, Faculty of Basic Sciences, Science and Research Branch, Islamic Azad University, Tehran, Iran.
Abstract:
IPS-1 and RIP1 are the main downstream molecules of RIG1 and MDA5, as intracytoplasmic receptors, which are the main receptors involved in recognition of internal and external viral double-stranded RNA. In this project, mRNA levels of IPS-1 and RIP1 were investigated in the peripheral blood immune cells of chronic hepatitis B (CHB) patients. IPS-1 and RIP1 mRNA levels were measured in 60 CHB patients and 120 healthy subjects, using RT-qPCR technique. A significant increase in expression levels of IPS-1 and RIP1 was found in patients when compared to healthy individuals. There was no correlation between IPS-1 and RIP1expression levels with the serum levels of hepatitis B e-Antigen (HBeAg) and liver enzymes in patients. Based on the results, it seems that IPS-1 and RIP1 can participate in the induction of low chronic inflammation, which is a main cause of liver cirrhosis and hepatocellular carcinoma.
Insights
Increased expression of IPS-1 and RIP1 in immune cells of chronic hepatitis B patients suggests their role in low-grade inflammation driving liver disease progression.
Area of Science:
- Immunology
- Virology
- Hepatology
Background:
- Intracytoplasmic receptors RIG1 and MDA5 recognize viral double-stranded RNA.
- IPS-1 and RIP1 are key downstream signaling molecules in this innate immune pathway.
Purpose of the Study:
- To investigate mRNA levels of IPS-1 and RIP1 in peripheral blood immune cells of chronic hepatitis B (CHB) patients.
- To explore the relationship between IPS-1/RIP1 expression and CHB disease markers.
Main Methods:
- Quantitative reverse transcription polymerase chain reaction (RT-qPCR) was used.
- mRNA levels of IPS-1 and RIP1 were measured in 60 CHB patients and 120 healthy controls.
Main Results:
- Significant elevation of IPS-1 and RIP1 mRNA levels was observed in CHB patients compared to healthy individuals.
- No correlation was found between IPS-1/RIP1 expression and serum HBeAg levels or liver enzymes.
Conclusions:
- IPS-1 and RIP1 may contribute to the chronic low-grade inflammation characteristic of CHB.
- This inflammation is implicated in the pathogenesis of liver cirrhosis and hepatocellular carcinoma.
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