Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
6
pubmed:dateCreated
1997-1-15
pubmed:abstractText
Circulating immune complexes (ICs) were isolated by affinity chromatography and sucrose density gradient fractionation during acute and chronic hepatitis C virus (HCV) infection. Immunochemical and biomolecular studies showed that they basically consist of the virus component, IgG with specific anti-HCV activity and IgM bearing 17.109 epitope (IgM 17.109), an antigenic determinant common to rheumatoid factors (RFs) with WA cross-idiotype (XId). An antigen-specific IC assay was used to demonstrate IgG anti-HCV/IgM 17.109 ICs (IgG-IgM ICs) in five out of the five patients with acute and in 8 out of the 10 patients with chronic hepatitis C who mounted an IgG anti-HCV immune response. They were not detected in patients with no IgG anti-HCV response. IgG-IgM ICs appeared in step with IgG anti-HCV seroconversion and remained detectable for a long period irrespective of clinical outcome, in that they were demonstrated over a 4-year follow-up of patients with chronic hepatitis C. Their presence was unrelated to the severity and progression of liver histology. Despite similar serum levels of IgM 17.109 XId, antigen-specific IgG-IgM ICs were not found in acute and chronic hepatitis B or in acute hepatitis A. Thus, these ICs appear to be uniquely associated with HCV infection, supporting the view that IgM 17.109 XId derive from an antigen-driven response strictly related to the involved antigen. Even although they have no apparent effects on the progression of HCV-related liver disease, their presence may help to explain the immunological abnormalities and extrahepatic disorders observed in HCV infection.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0014-2972
pubmed:author
pubmed:issnType
Print
pubmed:volume
26
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
465-75
pubmed:dateRevised
2006-11-15
pubmed:meshHeading
pubmed-meshheading:8817160-Acute Disease, pubmed-meshheading:8817160-Adolescent, pubmed-meshheading:8817160-Adult, pubmed-meshheading:8817160-Antigen-Antibody Complex, pubmed-meshheading:8817160-Biological Markers, pubmed-meshheading:8817160-Biopsy, pubmed-meshheading:8817160-Blotting, Western, pubmed-meshheading:8817160-Child, pubmed-meshheading:8817160-Female, pubmed-meshheading:8817160-Follow-Up Studies, pubmed-meshheading:8817160-Hepatitis, Chronic, pubmed-meshheading:8817160-Hepatitis A, pubmed-meshheading:8817160-Hepatitis B, pubmed-meshheading:8817160-Hepatitis C, pubmed-meshheading:8817160-Humans, pubmed-meshheading:8817160-Immunoglobulin G, pubmed-meshheading:8817160-Immunoglobulin M, pubmed-meshheading:8817160-Liver, pubmed-meshheading:8817160-Male, pubmed-meshheading:8817160-Middle Aged, pubmed-meshheading:8817160-Polymerase Chain Reaction, pubmed-meshheading:8817160-RNA, Viral, pubmed-meshheading:8817160-Time Factors
pubmed:year
1996
pubmed:articleTitle
Immunochemical and biomolecular studies of circulating immune complexes isolated from patients with acute and chronic hepatitis C virus infection.
pubmed:affiliation
Department of Biomedical Sciences and Human Oncology, University of Bari Medical School, Italy.
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't