Severe fletcher factor (plasma prekallikrein) deficiency with partial deficiency of hageman factor (factor xii): Report of a case with observation on in vivo and in vitro leukocyte chemotaxis
- 1 May 1982
- journal article
- research article
- Published by Wiley in American Journal of Hematology
- Vol. 12 (3) , 261-270
- https://doi.org/10.1002/ajh.2830120308
Abstract
A case of cross‐reacting material‐negative Fletcher trait with additional partial deficiency of Hageman factor (HF, Factor XII) is described. Although the patient presented with a recent history of frequent epistaxis, he had no other personal or family history of a tendency toward bleeding or infection. Similar to other cases of Fletcher trait, his plasma showed a markedly prolonged partial thromboplastin time which could be corrected by prolonged incubation with the surface‐activator kaolin. Surface‐induced fibrinolysis, amidolysis of α‐N‐benzoyl‐proline‐L‐phenylalanine‐L‐arginine‐p‐nitro‐ anilide, and cold‐promoted enhancement of factor VII activity, reactions requiring the presence in the plasma of Fletcher factor (pre‐kallikrein), in addition to Hageman factor and Fitzgerald factor (high‐molecular weight kininogen), were also defective. In vivo chemotaxis of polymorphonuclear leukocytes and monocytes (Rebuck's skin window technique) in response to skin abrasions was defective, but was normal when diphtheria‐tetanus toxoid was also applied. In vitro leukocyte chemotaxis (Boyden chamber technique) in response to normal or patient's own serum activated with zymosan was normal. Together with previous observations that kallikrein generated chemotactic activity, possibly via activation of C5, the present observations suggest that prekallikrein activation may be important for in vivo leukocyte chemotactic response to skin abrasion. The inheritance of Fletcher trait in this patient is unclear. Although the father was an apparent heterozygote, the mother was completely normal for Fletcher factor procoagulant activity and antigen. The mild Hageman factor deficiency in the patient did not contribute significantly to the plasma defects described and was likely inherited from the father who had a low HF procoagulant activity.Keywords
This publication has 29 references indexed in Scilit:
- Fletcher Factor Deficiency: Report of a New FamilyScandinavian Journal of Haematology, 2009
- Plasma Prekallikrein (Fletcher Factor) Deficiency in a Patient With Chronic Lymphocytic LeukemiaSouthern Medical Journal, 1980
- Fletcher Factor Deficiency and Myocardial InfarctionAmerican Journal of Clinical Pathology, 1976
- Fitzgerald TraitJournal of Clinical Investigation, 1975
- Defective Activation of Clotting, Fibrinolytic, and Permeability-Enhancing Systems in Human Fletcher Trait PlasmaCirculation Research, 1974
- Fletcher factor deficiency. A diminished rate of Hageman factor activation caused by absence of prekallikrein with abnormalities of coagulation, fibrinolysis, chemotactic activity, and kinin generation.Journal of Clinical Investigation, 1974
- A PREALBUMIN ACTIVATOR OF PREKALLIKREINThe Journal of Experimental Medicine, 1972
- Immunologic differentiation of classic hemophilia (factor VIII deficiency) and von Willebrand's diseaseJournal of Clinical Investigation, 1971
- Fletcher Factor Deficiency: A Report of Three Unrelated CasesBritish Journal of Haematology, 1970
- Quantitative estimation of proteins by electrophoresis in agarose gel containing antibodiesAnalytical Biochemistry, 1966