Volume 11, Issue 2 852358 pp. 129-133
Article
Open Access

Serial Analysis of Antimitochondrial Antibody in Patients with Primary Biliary Cirrhosis

Gordon D. Benson

Gordon D. Benson

Department of Medicine UMDNJ-Robert Wood Johnson Medical School Camden, NJ, USA , umdnj.edu

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Kentaro Kikuchi

Kentaro Kikuchi

Fourth Department of Internal Medicine Teikyo University School of Medicine Kanagawa, Japan , teikyo-u.ac.jp

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Hiroshi Miyakawa

Hiroshi Miyakawa

Fourth Department of Internal Medicine Teikyo University School of Medicine Kanagawa, Japan , teikyo-u.ac.jp

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Atsushi Tanaka

Atsushi Tanaka

Department of Medicine Teikyo University School of Medicine Tokyo, Japan , teikyo-u.ac.jp

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Mitchell R. Watnik

Mitchell R. Watnik

Division of Rheumatology Allergy and Clinical Immunology University of California at Davis School of Medicine Davis, CA, USA , ucdavis.edu

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M. Eric Gershwin

M. Eric Gershwin

Division of Rheumatology Allergy and Clinical Immunology University of California at Davis School of Medicine Davis, CA, USA , ucdavis.edu

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First published: 01 January 2004
Citations: 42

Abstract

Antimitochondrial antibodies (AMAs) are the classic serologic marker in primary biliary cirrhosis (PBC). However, there have been only limited attempts to study changes in titer or isotype analysis of such AMAs in patients followed for long periods of time

We took advantage of stored sera from well-characterized patients with PBC followed for a period of 7-28 years (mean duration of 13.5 years). Immunoblot and enzyme-linked immunosorbant assays were performed against PDC-E2, BCOADC-E2 and OGDC-E2 as well as isotype analysis of antigen-specific IgG, IgA and IgM antibodies against each of these mitochondrial autoantigens. Sera were analyzed for total IgG, IgA and IgM by radial immunodiffusion. The sera titer of AMAs was significantly higher in younger patients with PBC. Indeed, age of onset of clinical PBC was a significant predictor for the highest values of sera AMAs. In contrast, the AMA titer did not significantly change over time in this prolonged longitudinal study. The total sera levels of the individual immunoglobulins did not show a time-dependent change, when based on age of onset of the disease. Higher titers of AMAs were noted in the younger patients. Furthermore, despite this long follow-up, there was no evidence for a significant change in AMA levels; also, levels were not influenced by drug therapy used during the period of observation.

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