Thromb Haemost 2000; 84(04): 541-547
DOI: 10.1055/s-0037-1614064
Review Article
Schattauer GmbH

Discrimination of von Willebrands Disease (VWD) Subtypes: Direct Comparison of von Willebrand Factor:Collagen Binding Assay (VWF:CBA) with Monoclonal Antibody (MAB) Based VWF-capture Systems

Emmanuel J. Favaloro
1   From the Department of Haematology, Institute of Clinical Pathology and Medical Research (ICPMR), Westmead Hospital, Western Sydney Area Health Service, Westmead, NSW, Australia
,
Anthony Henniker
1   From the Department of Haematology, Institute of Clinical Pathology and Medical Research (ICPMR), Westmead Hospital, Western Sydney Area Health Service, Westmead, NSW, Australia
,
David Facey
1   From the Department of Haematology, Institute of Clinical Pathology and Medical Research (ICPMR), Westmead Hospital, Western Sydney Area Health Service, Westmead, NSW, Australia
,
Mark Hertzberg
1   From the Department of Haematology, Institute of Clinical Pathology and Medical Research (ICPMR), Westmead Hospital, Western Sydney Area Health Service, Westmead, NSW, Australia
› Author Affiliations
The authors would like to thank all the clinicians that send plasma samples to our laboratory for analysis, and Dr. Jerry Koutts for continued support and encouragement. The technical assistance of Rennie Coombs, who performed the Ristocetin Cofactor assays is also acknowledged. Finally, the staff of the Parramatta blood bank is thanked profusely for continued assistance.
Further Information

Publication History

Received 03 January 2000

Accepted after resubmission 08 May 2000

Publication Date:
11 December 2017 (online)

Summary

Discrimination of von Willebrand’s Disease (VWD) subtypes is important since it influences management. Qualitative [ie Type 2A, 2B, 2M] defects exhibit von Willebrand factor (VWF) discordance and give high VWF:Ag to VWF:’activity’ ratios. Classically, VWF:’activity’ is assessed using the VWF:RCof assay. The VWF:CBA is an ELISAbased VWF-functional adhesive assay which has consistently proved to be superior to VWF:RCof. A commercially available monoclonal antibody (MAB) based ELISA assay system claimed to mimic a VWF:RCof-like activity has also been recently described (‘SE’), as has the production and characterisation of a large number [n = 10] of locally generated anti-VWF MAB. In the current study, we have adapted these MAB to in-house ELISA assays to assess their utility for VWD diagnosis and subtype discrimination, and to compare them with other assay systems. Thus, the VWF:CBA, VWF:RCof by agglutination, the SE assay, and in-house MAB based assays have been directly compared for their ability to discriminate Type 1 [n = 9] from Type 2 VWD samples [phenotypes 2A and 2B; n = 11]. In summary, MAB-based systems can be used to measure VWF and confirm a diagnosis of VWD, as well as exhibiting some VWD-subtype-discriminatory capabilities. However, better evidence of VWF-discordance was usually achieved using the VWF:RCof (agglutination) assay, while the greatest degree of VWFdiscordance was consistently observed using the VWF:CBA assay. In conclusion, the VWF:CBA assay proved to offer the best diagnostic predictive tool for a Type 2 VWD defect, while MAB-based systems appear to be less effective in this regard.

Abbreviations: HMW: High Molecular Weight [VWF], MAB: Monoclonal antibody (/antibodies), PNP: Pooled Normal Plasma, RIPA: Ristocetin induced platelet aggregation, VWD: von Willebrands disease (/disorder), VWF: von Willebrand Factor, VWF:Ag: von Willebrand Factor Antigen (assay), VWF:CBA: Collagen Binding [Activity] Assay for VWF, VWF:RCof: Ristocetin Cofactor Assay for VWF

 
  • References

  • 1 Rodeghiero F, Castaman G, Dini E. Epidemiological investigation of the prevalence of von Willebrand’s disease. Blood 1987; 69: 454-9.
  • 2 Sadler JE, Gralnick HR. Commentary: A new classification for von Willebrand disease. Blood 1994; 84: 676-9.
  • 3 Sadler JE. A revised classification of von Willebrand disease. For the Subcommittee on von Willebrand factor of the Scientific and Standardisation Committee of the International Society on Thrombosis and Haemostasis. Thromb Haemost 1994; 71: 520-5.
  • 4 Ruggeri ZM. Structure and function of von Willebrand factor. Thromb Haemost 1999; 82: 576-84.
  • 5 Guidelines for the diagnosis and management of von Willebrand disease. Prepared by the von Willebrand Working Party of the United Kingdom Haemophilia Centre Directors’ Organisation. 1995
  • 6 Sadler JE, Foster PA, George JN. Haemostasis/Platelets. In: Haematology1996 (ed) McArthur JR. The Education Program of the American Society of Hematology 1996; 79-94.
  • 7 Favaloro EJ. Laboratory assessment as a critical component of the appropriate diagnosis and sub-classification of von Willebrand’s disease. Blood Reviews 1999; 13: 185-204.
  • 8 Favaloro EJ, Smith J, Petinos P, Collecutt M, Street A, Hertzberg M. on behalf of the RCPA Quality Assurance Program (QAP) in Haematology Scientific Haemostasis Advisory Panel (1999). Laboratory testing, diagnosis and management of von Willebrand’s disease: Current practice in Australasia. Am J Clin Pathol 1999; 112: 712-9.
  • 9 Favaloro EJ, Koutts J. Laboratory assays for von Willebrand factor: Relative contribution to the diagnosis of von Willebrand’s disease. Pathology 1997; 29: 385-91.
  • 10 Favaloro EJ, Smith J, Petinos P, Hertzberg H, Koutts J. on behalf of the RCPA Quality Assurance Program (QAP) in Haematology Haemostasis Scientific Advisory Panel. Laboratory testing for von Willebrand’s disease: An assessment of current diagnostic practice and efficacy by means of a multi-laboratory survey. Thromb Haemost 1999; 82: 1276-82.
  • 11 Favaloro EJ, Grispo L, Exner T, Koutts J. Development of a simple collagen based ELISA assay aids in the diagnosis of, and permits sensitive discrimination between Type I and Type II, von Willebrand’s disease. Blood Coagul and Fibrinolysis 1991; 02: 285-91.
  • 12 Favaloro EJ, Grispo L, Dinale A, Berndt M, Koutts J. von Willebrand’s Disease: Laboratory investigation using an improved functional assay for von Willebrand factor. Pathology 1993; 25: 152-8.
  • 13 Favaloro EJ, Facey D, Grispo L. Laboratory assessment of von Willebrand factor: Use of different assays can influence the diagnosis of von Willebrand’s disease, dependent on differing sensitivity to sample preparation and differential recognition of high molecular weight VWF forms. Am J Clin Pathol 1995; 104: 264-71.
  • 14 Favaloro EJ, Mehrabani PA, Koutts J. Laboratory assessment of von Willebrand factor: altered interpretation of laboratory data, and altered diagnosis of von Willebrand’s disease, as influenced by the use of different vWF assays and assay conditions. Clin Appl Thromb/Hemost 1997; 03: 110-8.
  • 15 Favaloro EJ, Dean M, Grispo L, Exner T, Koutts J. von Willebrand’s disease: Use of Collagen Binding Assay provides potential improvement to laboratory monitoring of desmopressin (DDAVP) therapy. Am J Hematol 1994; 45: 205-11.
  • 16 Ramasamy I, Farrugia A, Tran E, Anastasius V, Charnock A. Biological activity of von Willebrand factor during the manufacture of therapeutic factor VIII concentrates as determined by the collagen-binding assay. Biologicals 1998; 26: 155-66.
  • 17 Fischer BE, Kramer G, Mitterer A, Grillberger L, Reiter M, Mundt W, Dorner F, Eibl J. Effect of multimerisation of human and recombinant von Willebrand factor on platelet aggregation, binding to collagen and binding of coagulation factor VIII. Thromb Res 1996; 84: 55-66.
  • 18 Fischer BE, Thomas KB, Dorner F. von Willebrand factor: measuring its antigen or function? Correlation between the level of antigen, activity, and multimer size using various detection systems. Thromb Res 1998; 91: 39-43.
  • 19 Casonato A, Pontara E, Bertomoro A, Zucchetto S, Zerbinati P, Girlami A. Abnormal collagen binding activity of 2A von Willebrand factor: evidence that the defect depends only on the lack of large multimers. J Lab Clin Med 1997; 129: 251-9.
  • 20 Kempfer AC, Silaf MR, Farias CE, Carballo GA, Woods AI, Lazzari MA. Binding of von Willebrand Factor to Collagen by Flow Cytometry. Am J Clin Pathol 1999; 111: 418-23.
  • 21 Goodall AH, Jarvis J, Chand S, Rawlings E, O’Brien DP, McCraw A, Hutton R, Tuddenham EGD. An immunoradiometric assay for human factor VIII von Willebrand factor (VIII:VWF) using a monoclonal antibody based that defines a functional epitope. Br J Haematol 1985; 59: 565-77.
  • 22 Chand S, McCraw A, Hutton R, Tuddenham EGD, Goodall AH. A two-site, monoclonal antibody based immunoassay for von Willebrand factor-Demonstration that VWF function resides in a conformational epitope. Thromb Haemost 1986; 55: 318-24.
  • 23 Murdock PJ, Woodhams BJ, Mathews KB, Pasi KJ, Goodall AH. von Willebrand factor activity detected in a monoclonal antibody-based ELISA: an alternative to the Ristocetin cofactor platelet agglutination assay for diagnostic use. Thromb Haemost 1997; 78: 1272-7.
  • 24 Favaloro EJ. Collagen binding assay for von Willebrand factor (VWF:CBA): Detection of von Willebrands Disease (VWD), and discrimination of VWD subtypes, depends on collagen source. Thromb Haemost 2000; 83: 127-35.
  • 25 Preston FE. Assays for von Willebrand factor functional activity: A UK NEQAS Survey. Thromb Haemost 1998; 80: 863.
  • 26 Facey DA, Favaloro EJ, Koutts J, Berndt MC, Hertzberg M. Identification and characterisation of a novel mutation in von Willebrand factor causing a Type 2B von Willebrand’s disease. Br J Haematol 1999; 105: 538-41.
  • 27 Facey DA, Favaloro EJ, Maxwell E, Baker R, Hertzberg MS. Type 2B von Willebrand’s disease in thirteen individuals from five unrelated Australian Families: Phenotype and genotype correlations. American J Hematology 2000; 63: 197-9.
  • 28 De Luca M, Facey DA, Favaloro EJ, Hertzberg MS, Whisstock JC, McNally T, Andrews RK, Berndt MC. Structure and function of the von Willebrand factor A1 domain. Analysis with monoclonal antibodies reveals distinct binding sites involved in recognition of the platelet membrane glycoprotein Ib-IX-V complex and ristocetin-dependent activation. Blood 2000; 95: 164-72.
  • 29 Favaloro EJ, Facey D, Henniker A. Use of a novel Platelet Function Analyser (PFA-100™) with high sensitivity to disturbances in von Willebrand factor to screen for von Willebrand’s disease and other disorders. Am J Hematol 1999; 62: 165-74.
  • 30 Favaloro EJ, Bradstock KF, Kamath S, Dowden G, Gillis D, George V. Characterisation of a p43 human thymocyte antigen. Disease Markers 1986; 04: 261-70.
  • 31 Favaloro EJ, Bradstock KF, Grimsley P, Henniker A, Kamath S. Further studies on the heterogeneity of antigens recognised by CD-1 monoclonal antibodies: Distribution of epitopes and analysis of serological binding patterns. Immunol Cell Biol 1987; 65: 517-27.
  • 32 Siekmann J, Turecek PL, Fischer BE, Mitterer A, Schlokat U, Falkner F, Dorner F, Schwarz HP. Characterisation of plasma-derived and recombinant human VWF by improved collagen binding assays. Thromb Haemost 1995; 73: 1160.
  • 33 Fischer BE, Thomas KB, Dorner F. Collagen covalently immobilised onto plastic surfaces simplifies measurement of von Willebrand factor-collagen binding activity. Ann Hematol 1998; 76: 159-66.
  • 34 Siekmann J, Turecek PL, Schwarz HP. The determination of von Willebrand factor activity by collagen binding assay. Hemophilia 1998; 04 (Suppl. 03) 15-24.