Immunoglobulin M and A antibodies to hepatitis C core antigen in chronic hepatitis C virus infection. 1994

G K Lau, and R Lesniewski, and R G Johnson, and G L Davis, and J Y Lau
Department of Medicine, University of Florida, Gainesville 32610.

To determine the prevalence and clinical significance of IgM and IgA antibody to hepatitis C virus (HCV) core antigen in chronic HCV infection, sera from 47 patients were tested for immunoglobulin class M (IgM) and immunoglobulin A (IgA) antibody to HCV core antigen by solid-phase enzyme-linked immunoassay using a recombinant core protein (aa1-150). Results were correlated with the clinical, biochemical and histological parameters, serum HCV RNA levels (determined by branched DNA signal amplification assay), and subsequent clinical response to interferon-alpha therapy. IgM anti-HCV core was detected in 11 patients (23.4 percent). There was no correlation between the presence of IgM anti-HCV core and the clinical features (sex, age, mode of acquisition), biochemical parameters (serum ALT, AST, alkaline phosphatase, and albumin level), autoimmune markers [serum globulin levels, anti-nuclear antibody (+ at < 1:80 in 7/47 patients)], serum HCV RNA levels, subsequent response to interferon-alpha therapy, and the histological features. Immunoglobulin A anti-HCV core was not detected in any of the patients. The presence of IgM ant-HCV core in a proportion of patients with chronic HCV infection indicates that the presence of serum IgM anti-HCV core may not be unique to acute HCV infection.

UI MeSH Term Description Entries
D007070 Immunoglobulin A Represents 15-20% of the human serum immunoglobulins, mostly as the 4-chain polymer in humans or dimer in other mammals. Secretory IgA (IMMUNOGLOBULIN A, SECRETORY) is the main immunoglobulin in secretions. IgA,IgA Antibody,IgA1,IgA2,Antibody, IgA
D007075 Immunoglobulin M A class of immunoglobulin bearing mu chains (IMMUNOGLOBULIN MU-CHAINS). IgM can fix COMPLEMENT. The name comes from its high molecular weight and originally was called a macroglobulin. Gamma Globulin, 19S,IgM,IgM Antibody,IgM1,IgM2,19S Gamma Globulin,Antibody, IgM
D008297 Male Males
D008875 Middle Aged An adult aged 45 - 64 years. Middle Age
D002908 Chronic Disease Diseases which have one or more of the following characteristics: they are permanent, leave residual disability, are caused by nonreversible pathological alteration, require special training of the patient for rehabilitation, or may be expected to require a long period of supervision, observation, or care (Dictionary of Health Services Management, 2d ed). For epidemiological studies chronic disease often includes HEART DISEASES; STROKE; CANCER; and diabetes (DIABETES MELLITUS, TYPE 2). Chronic Condition,Chronic Illness,Chronically Ill,Chronic Conditions,Chronic Diseases,Chronic Illnesses,Condition, Chronic,Disease, Chronic,Illness, Chronic
D005260 Female Females
D006508 Hepatitis Antibodies Immunoglobulins raised by any form of viral hepatitis; some of these antibodies are used to diagnose the specific kind of hepatitis. Antibodies, Hepatitis
D006526 Hepatitis C INFLAMMATION of the LIVER in humans caused by HEPATITIS C VIRUS, a single-stranded RNA virus. Its incubation period is 30-90 days. Hepatitis C is transmitted primarily by contaminated blood parenterally and is often associated with transfusion and intravenous drug abuse. However, in a significant number of cases, the source of hepatitis C infection is unknown. Hepatitis, Viral, Non-A, Non-B, Parenterally-Transmitted,Parenterally-Transmitted Non-A, Non-B Hepatitis,PT-NANBH,Parenterally Transmitted Non A, Non B Hepatitis
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000328 Adult A person having attained full growth or maturity. Adults are of 19 through 44 years of age. For a person between 19 and 24 years of age, YOUNG ADULT is available. Adults

Related Publications

G K Lau, and R Lesniewski, and R G Johnson, and G L Davis, and J Y Lau
January 1984, Pathology,
G K Lau, and R Lesniewski, and R G Johnson, and G L Davis, and J Y Lau
April 1981, Journal of clinical microbiology,
G K Lau, and R Lesniewski, and R G Johnson, and G L Davis, and J Y Lau
October 1997, The American journal of gastroenterology,
G K Lau, and R Lesniewski, and R G Johnson, and G L Davis, and J Y Lau
October 1997, Journal of the Formosan Medical Association = Taiwan yi zhi,
G K Lau, and R Lesniewski, and R G Johnson, and G L Davis, and J Y Lau
October 1996, Transplantation proceedings,
G K Lau, and R Lesniewski, and R G Johnson, and G L Davis, and J Y Lau
August 1995, Hepatology (Baltimore, Md.),
G K Lau, and R Lesniewski, and R G Johnson, and G L Davis, and J Y Lau
July 2006, World journal of gastroenterology,
G K Lau, and R Lesniewski, and R G Johnson, and G L Davis, and J Y Lau
August 1985, Gastroenterology,
G K Lau, and R Lesniewski, and R G Johnson, and G L Davis, and J Y Lau
October 1992, Gastroenterology,
G K Lau, and R Lesniewski, and R G Johnson, and G L Davis, and J Y Lau
January 1984, American journal of clinical pathology,
Copied contents to your clipboard!