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Regulation of Toll-like receptor-2 expression in chronic hepatitis B by the precore protein†
Article first published online: 22 DEC 2006
Copyright © 2006 American Association for the Study of Liver Diseases
Volume 45, Issue 1, pages 102–110, January 2007
How to Cite
Visvanathan, K., Skinner, N. A., Thompson, A. J.V., Riordan, S. M., Sozzi, V., Edwards, R., Rodgers, S., Kurtovic, J., Chang, J., Lewin, S., Desmond, P. and Locarnini, S. (2007), Regulation of Toll-like receptor-2 expression in chronic hepatitis B by the precore protein. Hepatology, 45: 102–110. doi: 10.1002/hep.21482
Potential conflict of interest: Dr. Desmond advises for Schering-Plough, Roche, and Gilead. Dr. Locarnini is a consultant for and owns stock in Pharmasset. He is a consultant for, advises, receives grants from, and is on the speakers' bureau of Gilead. He is a consultant for and received grants from Bristol-Myers Squibb. He holds intellectual rights with Melbourne Health and Innogenetics. He is a consultant for Evivar Pty Ltd. He received grants from LG Sciences.
- Issue published online: 22 DEC 2006
- Article first published online: 22 DEC 2006
- Manuscript Accepted: 16 OCT 2006
- Manuscript Received: 28 MAY 2006
Toll-like receptors (TLRs) play a key role in the innate immune response. The aim of this study was to examine the expression of TLR2 and TLR4 in chronic hepatitis B (CHB). The TLR2 and TLR4 expression on hepatocytes and Kupffer cells from fresh liver biopsies was measured from 21 patients with untreated hepatitis B e antigen (HBeAg)-positive and HBeAg-negative CHB. Parallel studies were also undertaken on monocytes from their peripheral blood. Expression of TLR2 on hepatocytes, Kupffer cells, and peripheral monocytes was significantly reduced in patients with HBeAg-positive CHB in comparison with HBeAg-negative CHB and controls, whereas it was significantly increased in HBeAg-negative CHB compared with controls. The level of TLR4 expression did not differ significantly between the groups. These results were confirmed in vitro using hepatic cell lines transduced with recombinant HBV baculovirus expressing wild-type HBV (HBeAg-positive), precore stop codon (G1896A) mutant HBV (HBeAg-negative). The functional relevance of these findings was established by the demonstration of significantly reduced cytokine production (TNF-α) and phospho-p38 kinase expression in the presence of the HBeAg. In the absence of HBeAg, HBV replication was associated with up-regulation of the TLR2 pathway leading to increased TNF-α production. Conclusion: This study demonstrates a potentially important interaction between HBeAg, HBV, and the innate immune response. (HEPATOLOGY 2007;45:102–110.)