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Conference Paper: Viral specific T cells phenotypes and toll like receptors mRNA expression in CD8 cells of chronic hepatitis B patients
Title | Viral specific T cells phenotypes and toll like receptors mRNA expression in CD8 cells of chronic hepatitis B patients |
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Authors | |
Issue Date | 2006 |
Publisher | Blackwell Publishing Asia. |
Citation | Shanghai—Hong Kong International Liver Congress, Shanghai, China, 25–28 March 2006. In Journal of Gastroenterology and Hepatology, 2006, v. 21 n. S2, p. A136 How to Cite? |
Abstract | Background The clearance or persistence of hepatitis B virus(HBV) is affected by HBV-specific cytotoxic T-lymphocyte (CTL).Since toll like receptors (TLRs) may contribute to the viral specificT cells. But what and how the TLRs take their functions in chronichepatitis B (CHB) patients remains unknown.Aims To investigate the association of TLRs in CD8+ T cells andtheir relationship with CTL cells in chronic hepatitis B patients.Material and methods Peripheral blood mononuclear cells(PBMC) were collected from 28 HLA-A2+ patients. Group A (n =8) were patients with spontaneous resolution of CHB (anti-HBc plusanti-HBs positive) while Group B (n = 20) was HBeAg (+) CHBpatients. Ex-vivo model:The PBMC of these patients were co-culturedwith live hepatitis B virus (HBV) for 7 days. PBMC were stained forthe frequency of CD4, CD8, CD45RA, CD45RO and CCR7 byFACS analysis. Viral specific CD8 cells were tested by tetramer toHLA-A2 limited HBV peptides. CD8+ cells were isolated and TLRs-2, 3 4 and 7 mRNA level in CD8+ cells and HBV DNA were testedby real time PCR. Interferon-g secretion was tested by ELISpot.Results After co-culture, there was an increase in HBV-specificCD8+tetramer+ cells in Group A when compared with Group B(mean ± SD 1.971 ± 0.694% vs. 0.7 ± 0.362%, respectively, P 0.001).Interferon-γ secretion was higher in Group A when compared with ingroup B on day 7 after stimulation (SFC were 304.25 ± 156.12 inGroup A and 49.6 ± 46.04 in Group B, P = 0.0002).The HBV DNAin the ex-vivo model was lower in Group A from day-5 to Day-7 ofco-culture. The frequency of CD8+CD45RA-CCR7-cells before co-culture was similar in both groups In both groups, 90% of the HBV-specific CD8+ cells were CD45RA-CCR7- effecter-memory T cells.TLR2, 3 and 4 mRNA were higher expressed in Group A than inGroup B. But only TLR4 has statistic significance (mean ± SD 2.915± 1.536 in Group A vs. 1.010 ± 0.988 in Group B respectively, p0.006).Conclusion HBV-specific CD8+tetramer+ cells are higher inpatients with spontaneous resolution of chronic HBV. TLR4 may beassociated with activation T memory cell in response to HBV.There were no significant differences among the phenotypes ofCD8/tetramer positive cells between the two groups. |
Persistent Identifier | http://hdl.handle.net/10722/108467 |
ISSN | 2023 Impact Factor: 3.7 2023 SCImago Journal Rankings: 1.179 |
DC Field | Value | Language |
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dc.contributor.author | Zhang, HY | en_HK |
dc.contributor.author | Hui, CK | en_HK |
dc.contributor.author | Lee, PY | en_HK |
dc.contributor.author | Yueng, YH | en_HK |
dc.contributor.author | Luk, JMC | en_HK |
dc.contributor.author | Lau, G | en_HK |
dc.date.accessioned | 2010-09-26T00:40:52Z | - |
dc.date.available | 2010-09-26T00:40:52Z | - |
dc.date.issued | 2006 | en_HK |
dc.identifier.citation | Shanghai—Hong Kong International Liver Congress, Shanghai, China, 25–28 March 2006. In Journal of Gastroenterology and Hepatology, 2006, v. 21 n. S2, p. A136 | en_HK |
dc.identifier.issn | 0815-9319 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/108467 | - |
dc.description.abstract | Background The clearance or persistence of hepatitis B virus(HBV) is affected by HBV-specific cytotoxic T-lymphocyte (CTL).Since toll like receptors (TLRs) may contribute to the viral specificT cells. But what and how the TLRs take their functions in chronichepatitis B (CHB) patients remains unknown.Aims To investigate the association of TLRs in CD8+ T cells andtheir relationship with CTL cells in chronic hepatitis B patients.Material and methods Peripheral blood mononuclear cells(PBMC) were collected from 28 HLA-A2+ patients. Group A (n =8) were patients with spontaneous resolution of CHB (anti-HBc plusanti-HBs positive) while Group B (n = 20) was HBeAg (+) CHBpatients. Ex-vivo model:The PBMC of these patients were co-culturedwith live hepatitis B virus (HBV) for 7 days. PBMC were stained forthe frequency of CD4, CD8, CD45RA, CD45RO and CCR7 byFACS analysis. Viral specific CD8 cells were tested by tetramer toHLA-A2 limited HBV peptides. CD8+ cells were isolated and TLRs-2, 3 4 and 7 mRNA level in CD8+ cells and HBV DNA were testedby real time PCR. Interferon-g secretion was tested by ELISpot.Results After co-culture, there was an increase in HBV-specificCD8+tetramer+ cells in Group A when compared with Group B(mean ± SD 1.971 ± 0.694% vs. 0.7 ± 0.362%, respectively, P 0.001).Interferon-γ secretion was higher in Group A when compared with ingroup B on day 7 after stimulation (SFC were 304.25 ± 156.12 inGroup A and 49.6 ± 46.04 in Group B, P = 0.0002).The HBV DNAin the ex-vivo model was lower in Group A from day-5 to Day-7 ofco-culture. The frequency of CD8+CD45RA-CCR7-cells before co-culture was similar in both groups In both groups, 90% of the HBV-specific CD8+ cells were CD45RA-CCR7- effecter-memory T cells.TLR2, 3 and 4 mRNA were higher expressed in Group A than inGroup B. But only TLR4 has statistic significance (mean ± SD 2.915± 1.536 in Group A vs. 1.010 ± 0.988 in Group B respectively, p0.006).Conclusion HBV-specific CD8+tetramer+ cells are higher inpatients with spontaneous resolution of chronic HBV. TLR4 may beassociated with activation T memory cell in response to HBV.There were no significant differences among the phenotypes ofCD8/tetramer positive cells between the two groups. | - |
dc.language | eng | en_HK |
dc.publisher | Blackwell Publishing Asia. | en_HK |
dc.relation.ispartof | Journal of Gastroenterology and Hepatology | en_HK |
dc.title | Viral specific T cells phenotypes and toll like receptors mRNA expression in CD8 cells of chronic hepatitis B patients | en_HK |
dc.type | Conference_Paper | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0815-9319&volume=21 Suppl&spage=A136&epage=A136&date=2006&atitle=Viral+specific+T+cells+phenotypes+and+toll+like+receptors+mRNA+expression+in+CD8+cells+of+chronic+hepatitis+B+patients | en_HK |
dc.identifier.email | Hui, CK: ckh23@cam.ac.uk | en_HK |
dc.identifier.email | Lee, PY: nikkilee@hkucc.hku.hk | en_HK |
dc.identifier.email | Yueng, YH: yhyueng@HKUCC-COM.hku.hk | en_HK |
dc.identifier.email | Luk, JMC: jmluk@hkucc.hku.hk | en_HK |
dc.identifier.email | Lau, G: gkklau@netvigator.com | en_HK |
dc.identifier.authority | Luk, JMC=rp00349 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1111/j.1440-1746.2006.04409.x | - |
dc.identifier.hkuros | 137533 | en_HK |
dc.identifier.volume | 21 | en_HK |
dc.identifier.spage | 136 | en_HK |
dc.identifier.epage | 136 | en_HK |
dc.identifier.issnl | 0815-9319 | - |