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Dept of Infectious Diseases Shanghai Ruijin Hospital Jiaotong University School of Medicine

Pattern Recognition Receptors and HBV Infection. Role of Toll-like Receptors. Dept of Infectious Diseases Shanghai Ruijin Hospital Jiaotong University School of Medicine Qing Xie. HBsAg rate (%).  8: high. 2-7: medium. <2: low. HBV infection is still a major global

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Dept of Infectious Diseases Shanghai Ruijin Hospital Jiaotong University School of Medicine

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  1. Pattern Recognition Receptors and HBV Infection Role of Toll-like Receptors Dept of Infectious Diseases Shanghai Ruijin Hospital Jiaotong University School of Medicine Qing Xie

  2. HBsAg rate (%) 8: high 2-7: medium <2: low HBV infection is still a major global health care problem High prevelance Widely spread • 350 million chronic carriers worldwide • 9th leading causes of death • 75% of HBV carrier areAsian

  3. Nature History of HBV Infection HCC HBV Virons 6-15% 5年 3-5% Adult 12-20% Chronic HBV Infection Acute HBV Infection Chronic Hepatitis B Cirrhosis 5年 95% Children 20-23% 5年 Antiviral treatment Liver Failure Complete Response Partially Response Non Response Immune as a key factor influences the outcome and progression of disease

  4. Challenge: What mechanism of virus clearance of host?? How to do that?? Virus clearance resolved H O S T Central Role HBV Unable to clear virus Immune function of Host Persistent infection Progression of disease

  5. Three essential elements required in liver inflammation following HBV infection HBV VIRONS IMMUNOCYTES HEPATOCYTES

  6. Non antigenspecific-INNATE IMMUNITY LINK Cytokines Type I interferon IL-12 Granzyme B Plasmacytoid DC pDC Phagocytes Antigen presentation mDC Myeloid DC NK/T NK CD4+CD25+ Treg cell Tregs Antigen specific-ADAPTIVE IMMUNITY CD8 B Th17 CD4 调节性T细胞

  7. Host HBV Virons Type I IFN Induction Virus Clearance Activated Cytotoxic Response Host Immune Response is mediated by Pattern Recognition Receptors(PRR) which recognizes specific molecular or replication intermediator of virus particles.

  8. Pattern Recognition Receptors(PRR)

  9. Recent Studies found: • The close relationship between host innate immunity and the recognition of pathogen and clearance. • TLR as an important PRR,plays a central role in defence of virus invasion. • Different TLR can recognize various pathogen.

  10. G+bacteria G-bacteria Virus Virus Virus clearance

  11. What is a role of TLR in HBV infection?? HBV G+bacteria G-bacteria • Disturbance of TLR expression induces the persistent infection. • Abnormal of signal passway initiated by TLR induces the inability to clear HBV or overclearance, that leads to immunotolerance or immune injury. Virus clearance

  12. Requirement of DC involment in TLR-initiated antivirus response • Toll-like receptor (TLR)-mediated recognition of specific structures of invading pathogens initiates innate as • well as adaptive immune responses via antigen-presenting • cells (APCs). • DC represents the most potent antigen-presenting cells and thus plays an important role in the induction of innate and specific immune response.

  13. Distribution of TLR on DCs mDC： （myeloid dendritic cell，mDC） （ CD3、CD14、CD16、CD19、CD20、CD56） －BDCA1(CD1c)+ CD11c+ TLR1 TLR2 TLR3 TLR4 TLR5 TLR6 TLR8 pDC：（plasmacytoid dendritic cell, pDC） （ CD3、CD14、CD16、CD19、CD20、 CD56）－BDCA2+ BDCA4+ CD123+ TLR7 TLR9 TLR3、TLR7、TLR9 参与抗病毒免疫

  14. Scientific Questions? • Function of Myeloid and Plasmacytoid Dendritic Cells of Patients with CHB?? • Expression of TLR-3, TLR-9 in patients following HBV chronic infection??

  15. Study Populations CHB： 28 cases Healthy：22 cases Including criteria： （1）Serum HBsAg positive > 6 months. （2）Abnormal liver function for 2 times with 2 weeks apart， ALT>1.5 xU/L at screeing. （3）Serum HBeAg(+)，HBeAb(-). （4）Serum HBV-DNA>1×105 /L. （5）excluded liver cirrhosis by liver ultrasound （6）excluded HIV、HCV、HDV、HEV coinfection. （7）Not allowed to use antiviral treatment or immunmodulator within 6 months.

  16. Selection and preparation of pDC、mDC pDC BDCA4 DC isolation kir mDC BDCA1 DC siolation kit

  17. p>0.05 p<0.05 125 600 100 500 75 400 positive cell % MFI 300 50 200 25 100 0 0 controls patients controls patients n=18 n=18 n=28 n=28 Fig.3. TLR9 expression of isolated peripheral precursor pDCs of chronic HBV patients (n=28) and healthy controls (n=18). (A) No difference in the percentage of pDCs expressing TLR9 was found between the patients and the controls. (B) The MFI of TLR9 from patients were significantly reduced compared to controls. Data are expressed as mean±SD

  18. B A C Fig.4. Flow cytometric analysis for enumeration of pDCs.PBMCs were isolated and stained with the following antibodies：Lin-FITC( CD3,CD14, CD16,CD19,CD20,CD56), PE-BDCA-2, and APC-CD123. (A) Dead cells were excluded by forward side scatter analysis. (B) After gating on the lineage marker-negative fraction (R2), (C) the CD123/BDCA-2-double positive represents the plasmacytoid dendritic cells.

  19. 600 r =-0.646 p=0.02 500 400 300 ALT??(IU/L) 200 100 0 0.0 0.1 0.2 0.3 0.4 0.5 pDC/PBMC% A B p<0.05 0.75 0.50 pDC frequency% 0.25 0.00 CHB NS n=26 n=21 Fig.5. （A）In patients with CHB the relative numbers of pDCs were significantly reduced compared healthy controls(P<.05). (B) Correlation of the relative frequency of pDCs with the ALT levels in chronic HBV infection. The relative counts of pDCs were inversely correlated with ALT values ( P<.05; r﹦-0.645).

  20. B A C 4500 4000 3500 3000 2500 IFNa(pg/L) 2000 1500 1000 500 0 PBMC-pDC PBMC n=22 n=22 Fig.6. pDCs were the main source of IFN-αin the peripheral blood of humans. (A) An example of frequency analysis of pDCs in PBMCs. (B) PBMCs were analyzed by flow cytometer which showed pDCs were almost depleted. (C) PBMCs were separated with magnetic beads coupled to BDCA-4 antibodies and both fractions were stimulated with CpG-ODN 2216 , which show great amount of IFN-αin the supernatant of the BDCA-4-positive fraction compared to the BDCA-4-negative fraction.

  21. p>0.05 p<0.05 p>0.05 3000 30000 2000 2000 20000 IFN-a pg/ml 1000 TNF pg/ml 10000 1000 0 0 0 controls controls patients patients controls patients n=20 n=20 n=22 n=22 n=20 n=22 C B A IL-6 pg/ml Fig.7. Cytokine production by isolated peripheral precursor pDCs of chronic HBV patients (n=22) and healthy controls (n=20) after stimulation with CpG-ODN 2216.After 24 hours of stimulation, cytokine production was determined in the culture supernatants by specific ELISAs. (A) pDCs of patients were significantly impaired in their ability to produce IFN-αcompared to healthy controls. No difference was detected in the production of (B) TNF-αand (C) IL-6 between patients and healthy controls.

  22. The decrease of TLR9 expression ability by DC is related to HBV infection in DC？ Hepatology 2006;43(3):539-547 HBsAg HBcAg

  23. CONCLUSIONS 1. The TLR9 expression of circulating pDCs is reduced in patients with CHB. 2. pDCs are functionally impaired with the lower ability to produce IFN-α in patients, that may partly contribute to hepatitis B evading an adequate immune response, resulting in HBV persistent infection in host. 3. HBsAg and HBcAg were detectable in pDCs of patients suggest that functional impairment of pDCs may correlate with HBV infection of pDCs.

  24. 0h 0h 12h 12h 24h 48h 24h 48h Fig8. The levels of TLR3 expression on mDC of peripherial blood between contrl and patients. It shows that TLR3 level in control is increased following 24 hrs stimulaton, however the increase of TLR3 expression was delayed to 48 hrs following stimulation. P<0.05。

  25. * * Fig9. The changes of TLR3 mRNA by real-time PCR at various timepoints following stimulation.It shows TLR3 mRNA is increased significantly at 12 hrs, it recovers to the baseline at 24 hrs and 48 hrs. However the increase of TLR3 mRNA in CHB patients was observed at 48 hrs. *P<0.05。

  26. * Fig10. Expression of TBK1 mRNA on mDC by RT-PCR. There is no difference in TBK1 mRNA at baseline between control and patients (P>0.05)。TBK1 mRNA is increased significantly at 12 hrs when compared to baseline in control (P<0.05). There is no difference in TBK1 mRNA at 12hrs, 24hrs and 48hrs when conpared to baseline (P>0.05)。

  27. * Fig11. Expression of IFN-βmRNA by RT-PCR in mDC. There is no difference in at baseline between control and patients (P>0.05)。The level of IFN-βmRNA expression at 12 hrs is higher than at baseline in control (P<0.05). However there is no deifference between at various time points(P>0.05)。

  28. * Fig12. The detection of IFN-β by ELISA in supernatant on mDC following polyI:C stimulation.The level of IFN-β at baseline is very similar between two groups.There is no difference at various timepoints following stimulation in patients.However,the level of IFN-βis much higher at 12 hrs when compared to baseline.Also the difference was observed at 12hrs, 24hrs and 48 hrs between control and patients.

  29. CONCLUSIONS • The increase of expression level of TLR3 is slower and delayed in CH groups than HV groups. It contributes to the inability for the host to clear HBV. • The level of TBK1 molecular is quite low even following dsRNA stimulation, suggesting that abnormal of signal transduction passway may exist in HBV . • Our results suggest that dysfunction of TLR3 might play an important role in chronic HBV infection. It may provide new insights for understanding the mechanism of persistent HBV infection

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