Thromb Haemost 1985; 53(01): 080-085
DOI: 10.1055/s-0038-1661241
Original Article
Schattauer GmbH Stuttgart

Measurement of Autoantibodies Against Fibrinogen and Fibrin Degradation Products by Enzyme-Linked Immunoassay

A N Whitaker
The University of Queensland, Department of Medicine, Princess Alexandra Hospital, Brisbane, Australia
,
J R McFarlane
The University of Queensland, Department of Medicine, Princess Alexandra Hospital, Brisbane, Australia
,
E A Rowe
The University of Queensland, Department of Medicine, Princess Alexandra Hospital, Brisbane, Australia
,
K Lee
The University of Queensland, Department of Medicine, Princess Alexandra Hospital, Brisbane, Australia
,
P P Masci
The University of Queensland, Department of Medicine, Princess Alexandra Hospital, Brisbane, Australia
› Author Affiliations
Further Information

Publication History

Received 10 May 1984

Accepted 08 November 1984

Publication Date:
18 July 2018 (online)

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Summary

We have devised a simple enzyme immunoassay to detect and quantitate autoantibodies against derivatives of fibrinogen. This assay has been applied with a range of antigens including a fibrinogen lysate (containing X, Y, D and E), D dimer, D dimerE and a preparation of high molecular weight complexes derived from crosslinked fibrin. We have found that autoantibodies interacting with these antigens can be detected in varying concentrations in most sera from both normal subjects and patients with a variety of diseases and are evidently of mixed Ig class. These autoantibodies are directed against at least several cryptic antigens which appear during fibrinogen/fibrin degradation and some appear to be directed specifically against cross- linked fibrin derivatives. No clear disease correlates have yet emerged but a relationship between elevated levels and prior infective, thrombotic, inflammatory or traumatic disorders is likely. It is suggested that these autoantibodies may contribute to the catabolism of fibrinogen derivatives, provide a marker of thrombosis, and sometimes produce pathologic effects.