Volume 2, Issue 3 pp. 328S-333S
Article
Free Access

Hepatobiliary Clearance of IgA Immune Complexes Formed in the Circulation

Paul R. Harmatz

Corresponding Author

Paul R. Harmatz

Gastrointestinal and Nutrition Unit of the Children's Service and Clinical Immunology and Allergy Unit of the Medical Services, Massachusetts General Hospital and the Departments of Pediatrics and Medicine, Harvard Medical School, Boston, Massachusetts 02114

Paul Harmatz, M.D., Pediatric Gastrointestinal and Nutrition Unit, Massachusetts General Hospital, Boston, Massachusetts 02114.===Search for more papers by this author
Ronald E. Kleinman

Ronald E. Kleinman

Gastrointestinal and Nutrition Unit of the Children's Service and Clinical Immunology and Allergy Unit of the Medical Services, Massachusetts General Hospital and the Departments of Pediatrics and Medicine, Harvard Medical School, Boston, Massachusetts 02114

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Bruce W. Bunnell

Bruce W. Bunnell

Gastrointestinal and Nutrition Unit of the Children's Service and Clinical Immunology and Allergy Unit of the Medical Services, Massachusetts General Hospital and the Departments of Pediatrics and Medicine, Harvard Medical School, Boston, Massachusetts 02114

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Kurt J. Bloch

Kurt J. Bloch

Gastrointestinal and Nutrition Unit of the Children's Service and Clinical Immunology and Allergy Unit of the Medical Services, Massachusetts General Hospital and the Departments of Pediatrics and Medicine, Harvard Medical School, Boston, Massachusetts 02114

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W. Allan Walker

W. Allan Walker

Gastrointestinal and Nutrition Unit of the Children's Service and Clinical Immunology and Allergy Unit of the Medical Services, Massachusetts General Hospital and the Departments of Pediatrics and Medicine, Harvard Medical School, Boston, Massachusetts 02114

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First published: May/June 1982
Citations: 30

This study was also presented in part at the National Meeting of the American Gastroenterological Association, New York, New York, May, 1981.

Abstract

The formation and clearance of circulating IgA immune complexes from blood to bile was investigated in this study. The i.v. injection of either MOPC-315, an IgA M-component with anti-dinitrophenyl (DNP) specificity, or TEPC-15, an IgA M-component of a different specificity, was followed by i.v. injection of 125I-DNP10-bovine serum albumin (BSA) as the antigen. The formation and clearance of IgA immune complexes in the circulation of MOPC-315-treated, but not TEPC-15-treated animals was deømonstrated by immunoprecipitation with polyacrylamide beads coated with rabbit anti-mouse IgA. IgA-125I-DNP10-BSA complexes were identified in the bile from MOPC-315-treated, but not TEPC-15-treated animals utilizing this same immunoprecipitation technique. These observations suggest that the liver or bile ducts transport IgA immune complexes from blood into bile. The clearance of 125I-DNP10-BSA from the circulation was documented by coprecipitation with rabbit anti-BSA and BSA. The clearance of this circulating antigen was slower in the MOPC-315-treated than in the TEPC-15-treated animals suggesting that under the conditions of the present experiment, circulating antigen is cleared more slowly after IgA immune complex formation.

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