File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1007/BF02088140
- Scopus: eid_2-s2.0-0028169198
- PMID: 8082512
- WOS: WOS:A1994PJ30800029
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Hepatic expression of interferon-α in chronic hepatitis B virus infection
Title | Hepatic expression of interferon-α in chronic hepatitis B virus infection |
---|---|
Authors | |
Keywords | HBV IFN-α liver histology natural history |
Issue Date | 1994 |
Publisher | Springer New York LLC. The Journal's web site is located at http://springerlink.metapress.com/openurl.asp?genre=journal&issn=0163-2116 |
Citation | Digestive Diseases And Sciences, 1994, v. 39 n. 9, p. 2014-2021 How to Cite? |
Abstract | Hepatic expression of interferon-α (IFN-α) was examined by immunohistochemistry in 90 Chinese patients (M/F 67:23, age: 14-69) with a spectrum of hepatitis B virus (HBV)-related chronic liver diseases. Immunoreactive IFN-α was detected in sinusoidal cells in 79 patients (88%) and in mononuclear cells in 59 patients (65.6%). Patients with active liver diseases (chronic active hepatitis, active cirrhosis, N = 55) had a higher level of IFN-α expression compared to patients with inactive histology (N = 35; sinusoidal cells, P < 0.01; mononuclear cells, P < 0.01). Cytoplasmic HBsAg, nuclear HBcAg, and cytoplasmic HBcAg were detected in 79 (88%), 42 (47%), and 23 (27%) patients respectively. Expression of IFN-α in mononuclear cells correlated with the expression of cytoplasmic HBcAg (P < 0.05) but not with nuclear HBcAg or cytoplasmic HBsAg. When the patients were divided into four different phases according to the natural history of chronic HBV infection, patients in the active liver disease phase had higher IFN-α expression compared to the immunotolerant and late phase patients (P < 0.01). Using double immunohistochemical staining, both IFN-α and cytoplasmic HBcAg were frequently detected near inflammatory infiltrates but no correlation existed between the hepatic expression of HBsAg and IFN-α. These data indicate that IFN-α is expressed in the liver in HBV-related active liver diseases and that the reported suboptimal production of IFN-α by PBMC in HBV-related chronic active liver diseases may be due to a redistribution of the IFN-α-producing mononuclear cells into the liver, the site of inflammation. |
Persistent Identifier | http://hdl.handle.net/10722/162038 |
ISSN | 2023 Impact Factor: 2.5 2023 SCImago Journal Rankings: 1.068 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Fang, JWS | en_US |
dc.contributor.author | Wu, PC | en_US |
dc.contributor.author | Lai, CL | en_US |
dc.contributor.author | Lo, CK | en_US |
dc.contributor.author | Meager, A | en_US |
dc.contributor.author | Lau, JYN | - |
dc.date.accessioned | 2012-09-05T05:16:49Z | - |
dc.date.available | 2012-09-05T05:16:49Z | - |
dc.date.issued | 1994 | en_US |
dc.identifier.citation | Digestive Diseases And Sciences, 1994, v. 39 n. 9, p. 2014-2021 | en_US |
dc.identifier.issn | 0163-2116 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/162038 | - |
dc.description.abstract | Hepatic expression of interferon-α (IFN-α) was examined by immunohistochemistry in 90 Chinese patients (M/F 67:23, age: 14-69) with a spectrum of hepatitis B virus (HBV)-related chronic liver diseases. Immunoreactive IFN-α was detected in sinusoidal cells in 79 patients (88%) and in mononuclear cells in 59 patients (65.6%). Patients with active liver diseases (chronic active hepatitis, active cirrhosis, N = 55) had a higher level of IFN-α expression compared to patients with inactive histology (N = 35; sinusoidal cells, P < 0.01; mononuclear cells, P < 0.01). Cytoplasmic HBsAg, nuclear HBcAg, and cytoplasmic HBcAg were detected in 79 (88%), 42 (47%), and 23 (27%) patients respectively. Expression of IFN-α in mononuclear cells correlated with the expression of cytoplasmic HBcAg (P < 0.05) but not with nuclear HBcAg or cytoplasmic HBsAg. When the patients were divided into four different phases according to the natural history of chronic HBV infection, patients in the active liver disease phase had higher IFN-α expression compared to the immunotolerant and late phase patients (P < 0.01). Using double immunohistochemical staining, both IFN-α and cytoplasmic HBcAg were frequently detected near inflammatory infiltrates but no correlation existed between the hepatic expression of HBsAg and IFN-α. These data indicate that IFN-α is expressed in the liver in HBV-related active liver diseases and that the reported suboptimal production of IFN-α by PBMC in HBV-related chronic active liver diseases may be due to a redistribution of the IFN-α-producing mononuclear cells into the liver, the site of inflammation. | en_US |
dc.language | eng | en_US |
dc.publisher | Springer New York LLC. The Journal's web site is located at http://springerlink.metapress.com/openurl.asp?genre=journal&issn=0163-2116 | en_US |
dc.relation.ispartof | Digestive Diseases and Sciences | en_US |
dc.subject | HBV | - |
dc.subject | IFN-α | - |
dc.subject | liver histology | - |
dc.subject | natural history | - |
dc.subject.mesh | Adolescent | en_US |
dc.subject.mesh | Adult | en_US |
dc.subject.mesh | Age Factors | en_US |
dc.subject.mesh | Aged | en_US |
dc.subject.mesh | Asian Continental Ancestry Group | en_US |
dc.subject.mesh | Chronic Disease | en_US |
dc.subject.mesh | Cytoplasm - Chemistry | en_US |
dc.subject.mesh | Female | en_US |
dc.subject.mesh | Hepatitis B - Ethnology - Pathology | en_US |
dc.subject.mesh | Hepatitis B Antigens - Analysis | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Immunohistochemistry | en_US |
dc.subject.mesh | Interferon-Alpha - Analysis | en_US |
dc.subject.mesh | Interferon-Gamma - Analysis | en_US |
dc.subject.mesh | Liver - Chemistry | en_US |
dc.subject.mesh | Male | en_US |
dc.subject.mesh | Middle Aged | en_US |
dc.subject.mesh | Sensitivity And Specificity | en_US |
dc.title | Hepatic expression of interferon-α in chronic hepatitis B virus infection | en_US |
dc.type | Article | en_US |
dc.identifier.email | Lai, CL:hrmelcl@hku.hk | en_US |
dc.identifier.authority | Lai, CL=rp00314 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1007/BF02088140 | en_US |
dc.identifier.pmid | 8082512 | - |
dc.identifier.scopus | eid_2-s2.0-0028169198 | en_US |
dc.identifier.hkuros | 5150 | - |
dc.identifier.volume | 39 | en_US |
dc.identifier.issue | 9 | en_US |
dc.identifier.spage | 2014 | en_US |
dc.identifier.epage | 2021 | en_US |
dc.identifier.isi | WOS:A1994PJ30800029 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Fang, JWS=7402963750 | en_US |
dc.identifier.scopusauthorid | Wu, PC=7403119323 | en_US |
dc.identifier.scopusauthorid | Lai, CL=7403086396 | en_US |
dc.identifier.scopusauthorid | Meager, A=7007068182 | en_US |
dc.identifier.scopusauthorid | Lau, JYN=7402446047 | en_US |
dc.identifier.issnl | 0163-2116 | - |