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- Publisher Website: 10.1016/0270-9139(93)90347-P
- Scopus: eid_2-s2.0-0027172231
- PMID: 7689528
- WOS: WOS:A1993LV01800004
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Article: Antibody response to core, envelope and nonstructural hepatitis C virus antigens: Comparison of immunocompetent and immunosuppressed patients
Title | Antibody response to core, envelope and nonstructural hepatitis C virus antigens: Comparison of immunocompetent and immunosuppressed patients |
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Authors | |
Issue Date | 1993 |
Publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www.hepatology.org/ |
Citation | Hepatology, 1993, v. 18 n. 3, p. 497-502 How to Cite? |
Abstract | Some immunosuppressed patients with hepatitis C virus infection do not have detectable levels of antibody to hepatitis C virus on second-generation enzyme immunoassay. Antibodies to the envelope and nonstructural region 5 proteins have not been examined. Four groups of patients with hepatitis C virus infection were studied: (a) 20 immunocompetent patients, (b) 15 hemodialysis patients, (c) 17 kidney transplant recipients and (d) 3 acute leukemia patients who underwent bone marrow transplantation. Serum samples were tested for antibody to hepatitis C virus with a second-generation enzyme immunoassay and multiantigen enzyme immunoassays and for hepatitis C virus RNA with a nested polymerase chain reaction assay. All the immunocompetent patients reacted to C25, C22 and C33C; 90% reacted to nonstructural region 5 antigen and 80% reacted to C100-3. Only 55% reacted against yeast-derived e1 and e2 antigens, but all reacted against vaccinia virus-expressed N e1 and e2 antigens, indicating that the envelope epitopes are conformational and glycosylated. Sixty-five percent to 90% of dialysis and kidney transplant patients reacted to C25, C22 and N e1 and e2, but only 12% to 60% reacted to C100-3, C33C and nonstructural region 5 antigen. Diminution or loss of reactivity to hepatitis C virus antigens was observed after kidney and bone marrow transplantation, with C25 and N e1 and e2 less affected. Our data suggest that incorporation of C25 and N e1 and e2 antigens in the assay for antibody to hepatitis C virus would improve the detection of hepatitis C virus infection in immunosuppressed patients. |
Persistent Identifier | http://hdl.handle.net/10722/161964 |
ISSN | 2023 Impact Factor: 12.9 2023 SCImago Journal Rankings: 5.011 |
ISI Accession Number ID |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Lok, ASF | en_US |
dc.contributor.author | Chien, D | en_US |
dc.contributor.author | Choo, QL | en_US |
dc.contributor.author | Chan, TM | en_US |
dc.contributor.author | Chiu, EKW | en_US |
dc.contributor.author | Cheng, IKP | en_US |
dc.contributor.author | Houghton, M | en_US |
dc.contributor.author | Kuo, G | en_US |
dc.date.accessioned | 2012-09-05T05:16:20Z | - |
dc.date.available | 2012-09-05T05:16:20Z | - |
dc.date.issued | 1993 | en_US |
dc.identifier.citation | Hepatology, 1993, v. 18 n. 3, p. 497-502 | en_US |
dc.identifier.issn | 0270-9139 | en_US |
dc.identifier.uri | http://hdl.handle.net/10722/161964 | - |
dc.description.abstract | Some immunosuppressed patients with hepatitis C virus infection do not have detectable levels of antibody to hepatitis C virus on second-generation enzyme immunoassay. Antibodies to the envelope and nonstructural region 5 proteins have not been examined. Four groups of patients with hepatitis C virus infection were studied: (a) 20 immunocompetent patients, (b) 15 hemodialysis patients, (c) 17 kidney transplant recipients and (d) 3 acute leukemia patients who underwent bone marrow transplantation. Serum samples were tested for antibody to hepatitis C virus with a second-generation enzyme immunoassay and multiantigen enzyme immunoassays and for hepatitis C virus RNA with a nested polymerase chain reaction assay. All the immunocompetent patients reacted to C25, C22 and C33C; 90% reacted to nonstructural region 5 antigen and 80% reacted to C100-3. Only 55% reacted against yeast-derived e1 and e2 antigens, but all reacted against vaccinia virus-expressed N e1 and e2 antigens, indicating that the envelope epitopes are conformational and glycosylated. Sixty-five percent to 90% of dialysis and kidney transplant patients reacted to C25, C22 and N e1 and e2, but only 12% to 60% reacted to C100-3, C33C and nonstructural region 5 antigen. Diminution or loss of reactivity to hepatitis C virus antigens was observed after kidney and bone marrow transplantation, with C25 and N e1 and e2 less affected. Our data suggest that incorporation of C25 and N e1 and e2 antigens in the assay for antibody to hepatitis C virus would improve the detection of hepatitis C virus infection in immunosuppressed patients. | en_US |
dc.language | eng | en_US |
dc.publisher | John Wiley & Sons, Inc. The Journal's web site is located at http://www.hepatology.org/ | en_US |
dc.relation.ispartof | Hepatology | en_US |
dc.subject.mesh | Antibody Formation | en_US |
dc.subject.mesh | Antigens, Viral - Immunology | en_US |
dc.subject.mesh | Blood Transfusion - Adverse Effects | en_US |
dc.subject.mesh | Bone Marrow Transplantation - Immunology | en_US |
dc.subject.mesh | Hiv Seropositivity | en_US |
dc.subject.mesh | Hepacivirus - Immunology | en_US |
dc.subject.mesh | Hepatitis Antibodies - Blood | en_US |
dc.subject.mesh | Hepatitis C - Immunology - Transmission | en_US |
dc.subject.mesh | Hepatitis C Antibodies | en_US |
dc.subject.mesh | Humans | en_US |
dc.subject.mesh | Immunocompetence | en_US |
dc.subject.mesh | Immunosuppression | en_US |
dc.subject.mesh | Kidney Transplantation - Immunology | en_US |
dc.subject.mesh | Leukemia - Surgery | en_US |
dc.subject.mesh | Renal Dialysis | en_US |
dc.subject.mesh | Viral Core Proteins - Immunology | en_US |
dc.subject.mesh | Viral Envelope Proteins - Immunology | en_US |
dc.subject.mesh | Viral Nonstructural Proteins - Immunology | en_US |
dc.title | Antibody response to core, envelope and nonstructural hepatitis C virus antigens: Comparison of immunocompetent and immunosuppressed patients | en_US |
dc.type | Article | en_US |
dc.identifier.email | Chan, TM:dtmchan@hku.hk | en_US |
dc.identifier.authority | Chan, TM=rp00394 | en_US |
dc.description.nature | link_to_subscribed_fulltext | en_US |
dc.identifier.doi | 10.1016/0270-9139(93)90347-P | en_US |
dc.identifier.pmid | 7689528 | - |
dc.identifier.scopus | eid_2-s2.0-0027172231 | en_US |
dc.identifier.volume | 18 | en_US |
dc.identifier.issue | 3 | en_US |
dc.identifier.spage | 497 | en_US |
dc.identifier.epage | 502 | en_US |
dc.identifier.isi | WOS:A1993LV01800004 | - |
dc.publisher.place | United States | en_US |
dc.identifier.scopusauthorid | Lok, ASF=35379868500 | en_US |
dc.identifier.scopusauthorid | Chien, D=7005297134 | en_US |
dc.identifier.scopusauthorid | Choo, QL=36501374700 | en_US |
dc.identifier.scopusauthorid | Chan, TM=7402687700 | en_US |
dc.identifier.scopusauthorid | Chiu, EKW=24827833600 | en_US |
dc.identifier.scopusauthorid | Cheng, IKP=7102537483 | en_US |
dc.identifier.scopusauthorid | Houghton, M=7007018686 | en_US |
dc.identifier.scopusauthorid | Kuo, G=16750292700 | en_US |
dc.identifier.issnl | 0270-9139 | - |