Cofactor of the “Lupus Anticoagulant”
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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This phenomenon has been termed the lupus cofactor effect.
“This phenomenon has been termed the lupus cofactor effect.8,9”
From A “Percent Correction” Formula for Evaluation of Mixing Studies (2002) · cites this paper as [9]
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McNeil, H. P., Chesterman, C. N., & Krilis, S. A. (1991) · Advances in immunology · doi:10.1016/s0065-2776(08)60777-4 · Cited by 481 · see citing works
A “Percent Correction” Formula for Evaluation of Mixing Studies
Chang, S.-H., Tillema, V., & Scherr, D. (2002) · American Journal of Clinical Pathology · doi:10.1309/rrek-8l6m-d2kc-hwlh · Cited by 67 · see citing works
Lupus anticoagulant test persistence over time and its associations with future thrombotic events
Colling, M. E., Ay, C., Kraemmer, D., Koder, S., Quehenberger, P., Pabinger, I., Posch, F., & Gebhart, J. (2022) · Blood Advances · doi:10.1182/bloodadvances.2021006011 · Cited by 5 · see citing works
- Authors
- Rivard, G. E., Schiffman, S., & Rapaport, S. I.
- Affiliations
- University of Southern California (US)
- Venue
- Thrombosis and Haemostasis
- Publisher
- Georg Thieme Verlag KG
- 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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