Cited by 35Systemic Lupus Erythematosus ResearchBlood Coagulation and Thrombosis MechanismsHemophilia Treatment and Research

Cofactor of the “Lupus Anticoagulant”

Rivard, Georges E., Schiffman, Sandra, Rapaport, Samuel I.·1974·Thrombosis and Haemostasis

Abstract

Summary Normal plasma contains an activity known as cofactor which further lengthens the clotting time of the plasma of some patients with the “lupus anticoagulant.55 Cofactor has been characterized as either prothrombin or a gamma globulin. Our findings indicate that cofactor has the following properties: stable at room temperature but largely destroyed by heating for 30 min at 56° C; sparingly adsorbed by Al(OH)3 or BaS04; apparent molecular weight on gel filtration around 200,000 daltons ; precipit- able between 50-75% ammonium sulfate saturation. Cofactor was present in plasmas from patients with hereditary deficiencies of factor II, V, VII, VIII, IX, X, XI, XII, or Fletcher factor; however, less cofactor activity was demonstrable in plasmas deficient in factor II, V, or X than in normal plasma or the other deficiency plasmas. Plasma from patients receiving oral anticoagulant therapy had variable levels of cofactor activity which could not be correlated with levels of factor II, VII, IX, X, or staphylocoagulase-reacting factor. Cofactor activity was unaffected by treatment with an anti-human immunoglobulin antiserum. These data support the conclusion that the cofactor reacting with our patient’s “lupus anticoagulant55 is neither prothrombin nor an immunoglobulin, but rather a unique molecule with some properties in common with each.

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Crossref · 10.1055/s-0038-1647724

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Authors
Rivard, G. E., Schiffman, S., & Rapaport, S. I.
Affiliations
University of Southern California (US)
Venue
Thrombosis and Haemostasis
Published
1974
Volume
32
Issue
02/03
Pages
554-563
ISSN
  • 0340-6245 (ISSN-L)
  • 2567-689X
OpenAlex
W2411742303
Cited by
35
References
0
Citations by year
2024: 2 · 2022: 1 · 2021: 1 · 2020: 1 · 2017: 1
FWCI
1.73
Type
journal article
Language
en
Open access
closed
Locations
  • Thrombosis and Haemostasis (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Rheumatology › Systemic Lupus Erythematosus Research
  • Health Sciences › Medicine › Hematology › Blood Coagulation and Thrombosis Mechanisms
  • Health Sciences › Medicine › Hematology › Hemophilia Treatment and Research
Keywords
lupus anticoagulant, cofactors, prothrombin, gamma globulin, plasma coagulation, factor deficiency, oral anticoagulants, immunoglobulins, molecular weight, thermal stability
MeSH terms
Anticoagulants, Blood Coagulation Disorders, Blood Coagulation Factors, Hemophilia B, Factor V Deficiency, Factor VII Deficiency, Factor X Deficiency, Factor XI Deficiency, Factor XII Deficiency, gamma-Globulins, Hot Temperature, Hemophilia A, Humans, Hypoprothrombinemias, Immunoglobulins, Lupus Erythematosus, Systemic, Molecular Weight, Chemical Precipitation

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