RSS-Feed abonnieren
DOI: 10.1055/s-0038-1646048
Fibrinolytic Response and Fibrin Fragment D-Dimer Levels in Patients with Deep Vein Thrombosis
Publikationsverlauf
Received 17. März 1987
Accepted after revision 17. August 1987
Publikationsdatum:
29. Juni 2018 (online)

Summary
An enzyme-linked immunosorbent assay for fragment D-dimer was developed with the use of two monoclonal antibodies directed against specific non-overlapping antigenic determinants, present in fragment D-dimer of crosslinked fibrin but not in fragment D of non crosslinked fibrin or of fibrinogen, The lower limit of sensitivity of the assay when applied to human plasma, is 25 ng/ml. Concentration of fragment D-dimer in plasma from healthy individuals was 177 ,± 83 ng/ml (mean ± SD). In plasma of 11 out of 12 patients with phlebographically confirmed acute deep vein thrombosis, fragment D-dimer levels were significantly increased. Fragment D-dimer was not increased in 9 out of 10 patients with recurrent idiopathic deep vein thrombosis during clinically silent episodes.
Total t-PA antigen and free t-PA antigen concentrations were measured using previously developed ELISAs. Nine of the 12 patients with acute deep vein thrombosis showed a significant increase of total t-PA antigen (from 8.6 ± 6.9 ng/ml to 21 ± 16 ng/ml) after venous occlusion but in 3 of these free t-PA remained undetectable. Five of the 10 patients with recurrent deep vein thrombosis responded to venous occlusion with a significant increase of total t-PA antigen (from 6.7±3.2 ng/ml to 14 ± 7.9 ng/ml) but, in all patients, free t-PA antigen remained undetectable.
It is concluded that the combined assays of total and free t-PA antigen and of fragment D-dimer may be useful for the evaluation of the dynamics of the fibrinolytic system in physiological and pathological conditions.
-
References
- 1 Marder VJ, Shulman NR, Caroll WR. High molecular weight derivatives of human fibrinogen produced by plasmin: I. Physicochemical and immunological characterizations. J Biol Chem 1969; 144: 2111-2119
- 2 Gaffney PJ. Breakdown products of fibrin and fibrinogen: molecular mechanisms and clinical implications. J Clin Pathol 1980; 33 (Suppl.) 10-17
- 3 Gaffney PJ, Brasher M. Subunit structure of the plasmin-induced degradation products of crosslinked fibrin. Biochem Biophys Acta 1973; 295: 308-313
- 4 Lee-Own V, Gordon YB, Chard T. The detection of neoantigenic sites on the D-dimer peptide isolated from plasmin digested cross-linked fibrin. Thromb Res 1979; 14: 77-84
- 5 Budzynski AZ, Marder VJ, Parker ME, Shames P, Brizuela BS, Olexa S. Antigenic markers on fragment DD: a unique plasmic derivative of human crosslinked fibrin. Blood 1979; 54: 794-804
- 6 Purves LR, Lindsey GG, Franks JJ. Sites of D-domain interaction in fibrin-derived D-dimer. Biochemistry 1980; 19: 4051-4058
- 7 Gaffney PJ. Distinction between fibrinogen and fibrin degradation products in plasma. Clin Chim Acta 1975; 65: 109-115
- 8 Lane DA, Preston FE, Van Ross ME, Kakkar VV. Characterization of serum fibrinogen and fibrin fragment produced during disseminated intravascular coagulation. Br J Haematol 1978; 40: 609-615
- 9 Whitaker AN, Rowe EA, Masci PP, Gaffney PJ. Identification of D-dimer-E complex in disseminated intravascular coagulation. Thromb Res 1980; 18: 453-459
- 10 Merskey C, Johnson AJ, Harris JV, Wang MT, Swain S. Isolation of fibrinogen-fibrin related antigen from human plasma by immuno-nffinity chrnmntogmphy its ehjuaclcrizalioii in normal subjects and in defibrinating patients with abruptio placentae and disseminated cancer. Br J Haematol 1980; 44: 655-670
- 11 Gracff H, Hafter R. Detection and relevance of ciosbliuked fibiin deiivatives m blood. Sem Thromb Hemostas 1982; 8: 57-68
- 12 Yoshioka K, Mizunos Miyata H, Maki S. Distinction between fibrinogen and fibrin degradation products produced during disseminated intravascular coagulation in childhood. Eur J Pediat 1982; 138: 46-48
- 13 Whitaker AN, Elms MJ, Masci PP, Bundesen PG, Rylatt DB, Webber AJ, Bunce IH. Measurement of crosslinked fibrin derivatives in plasma: an immunoassay using monoclonal antibodies. J Clin Pathol 1984; 37: 882-887
- 14 Elms MJ, Bunce H, Bundesen PG, Rylatt DB, Webber AJ, Masci PP, Whitaker AN. Measurement of crosslinked fibrin degradation products. An immunoassay using monoclonal antibodies. Thromb Haemostas 1983; 50: 591-594
- 15 Deutsch DG, Mertz ET. Plasminogen: purification from human plasma by affinity chromatography. Science 1970; 170: 1095-1096
- 16 Chase Jr T, Shaw E. Titration of trypsin, plasmin and thrombin with p-nitrophcnyl-p-guanidinobeiizuate HC1. Metli Enzyinol 1970; 19: 20-27
- 17 Blombäck B, Blombäck M. Fuiificatioii of human and bovine fibrinogen. Arkiv Kemi 1956; 10: 415
- 18 Collen D, Kudryk B, Hessel B, Blombäck B. Primary structure of human fibrinogen and fibrin. Isolation and partial characterization of chains of fragment D. J Biol Chem 1975; 250: 5808-5817
- 19 Haverkate F, Timan G. Protective effect of calcium in the plasmin degradation of fibrinogen and fibrin fragment D. Thromb Res 1977; 10: 803-812
- 20 Bini A, Semeraro N, Collen D. Affinity chromatography of soluble fibrin in human plasma on insolubilized fibrinogen and on fragment D from fibrinogen, non crosslinked or crosslinked fibrin. Thromb Res 1978; 13: 443-451
- 21 Kearney JF, Radbruch A, Liesegang B, Rajewski K. A new mouse myeloma cell line that has lost immunoglobulin expression but permits the construction of antibody-secreting hybrid cell lines. J Immunol 1979; 123: 1548-1550
- 22 Fazekas deSt-Groth, Scheidegger D. Production of monoclonal antibodies: strategy and tactics. J Immunol Meth 1986; 35: 1-21
- 23 Köhler G, Milstein C. Continuous cultures of fused cells secreting antibody of predefined specificity. Nature 1975; 256: 495-497
- 24 Anderson PN, Potter M. Induction of plasma cell tumors in Balb/c mice with 2, 6, 10, 14 tetramethyl-pentadecane (pristane). Nature 1969; 222: 994-995
- 25 Ey PL, Prowse SJ, Jenkin CR. Isolation of pure IgGl, IgG2a and IgG2b immunoglobulin from mouse serum using protein A-Sephar-ose. Immunochemistry 1978; 15: 429-436
- 26 Nakane PA, Kawaoi A. Peroxidase-labeled antibody. A new method for conjugation. J Histochem Cytochem 1974; 22: 1084-1091
- 27 Laemmli UK. Cleavage of structural proteins during the assembly of the head bacteriophage T4. Nature 1970; 227: 680-685
- 28 Axen R, Porath J, Ernback S. Chemical coupling of peptides and proteins to polysaccharides by means of cvanogen halides. Nature 1967; 214: 1302-1304
- 29 Vermylen C, De Vreker RA, Verstraete M. A rapid enzymatic method for assay of fibrinogen; the fibrin polymerization test (FPT). Clin Chim Acta 1963; 8: 418-424
- 30 Holvoet P, Cleemput H, Collen D. Assay of human tissue-type plasminogen activator (t-PA) with an enzyme-linked immunosorbent assay (ELISA) based on three murine monoclonal antibodies. Thromb Haemostas 1985; 54: 684-687
- 31 Holvoet P, Boes J, Collen D. Measurement of free, one-chain tissue-type plasminogen activator in human plasma with an enzyme-linked immunosorbent assay based on an active site specific murine monoclonal antibody. Blood 1987; 69: 284-289
- 32 Collen D, Lijnen HR. The fibrinolytic system in man. In: David S. Critical reviews in Oncology/Hematology. Vol.4. Issue 3 CRC Press; 1986: 249-301
- 33 Isacson S, Nilsson IM. Defective fibrinolysis in blood and vein walls in recurrent idiopathic venous thrombosis. Acta Chir Scand 1972; 138: 313-319
- 34 Korninger C, Lechner K, Niessner H, Gossinger H, Kundi M. Impaired fibrinolytic capacity predisposes for recurrences of venous thrombosis. Thromb Haemostas 1984; 52: 127-130
- 35 Bergsdorf N, Nilson T, Wallen P. An enzyme linked immunosorbent assay for determination of tissue type plasminogen activator applied to patients with thrombotic disease. Thromb Haemostas 1983; 50: 740-744
- 36 Nilsson IM, Ljungner HL, Tengborn L. Two different mechanisms in patients with venous thrombosis and defective fibrinolysis: low concentration of plasminogen activator or increased concentration of plasminogen activator inhibitor. Br Med J 1985; 290: 1453-1456
- 37 Hunt FA, Rylatt DB, Hart RA, Bundesen PG. Serum crosslinked fibrin and fibrinogen fibrin degradation products in disorders associated with activation of the coagulation on fibrinolytic systems. Br J Haematol 1985; 60: 715-722