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Seminars in Hematology
Volume 41, Issue 1
, Pages 75-82
, January 2004
Von Willebrand factor-cleaving protease (ADAMTS-13) activity determination in the diagnosis of thrombotic microangiopathies: the Swiss experience
References
- . Increasing mortality from thrombotic thrombocytopenic purpura in the United States—Analysis of national mortality data, 1968–1991. Am J Hematol. 1995;50:84–90
- . Management of thrombotic thrombocytopenic purpura. Br J Haematol. 2000;109:496–507
-
.
Hyaline thrombosis of the terminal arterioles and capillaries (A hitherto undescribed disease).
Proc NY Pathol Soc. 1924;24:21–24
-
.
Thrombotic thrombocytopenic purpura.
Blood. 1947;2:542–544
- . Thrombotic microangiopathies. N Engl J Med. 2002;347:589–600
- Unusually large plasma factor VIII (von Willebrand factor multimers in chronic relapsing thrombotic thrombocytopenic purpura). N Engl J Med. 1982;307:1432–1435
- . Heterogeneity of plasma von Willebrand factor multimers resulting from proteolysis of the constituent subunit. J Clin Invest. 1991;88:774–782
- . Partial purification and characterization of a protease from human plasma cleaving von Willebrand factor to fragments produced by in vivo proteolysis. Blood. 1996;87:4223–4234
- . Physiologic cleavage of von Willebrand factor by a plasma protease is dependent on its conformation and requires calcium ion. Blood. 1996;87:4235–4244
- . Deficient activity of von Willebrand factor-cleaving protease in chronic relapsing thrombotic thrombocytopenic purpura. Blood. 1997;89:3097–3103
- . Acquired deficiency of von Willebrand factor-cleaving protease in a patient with thrombotic thrombocytopenic purpura. Blood. 1998;91:2839–2846
- Von Willebrand factor-cleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome. N Engl J Med. 1998;339:1578–1584
- . Antibodies to von Willebrand factor-cleaving protease in acute thrombotic thrombocytopenic purpura. N Engl J Med. 1998;339:1585–1594
- . Purification of human von Willebrand factor-cleaving protease and its identification as a new member of the metalloproteinase family. Blood. 2001;98:1662–1666
- . Partial amino acid sequence of purified von Willebrand factor-cleaving protease. Blood. 2001;98:1654–1661
- . Structure of von Willebrand factor-cleaving protease (ADAMTS13), a metalloprotease involved in thrombotic thrombocytopenic purpura. J Biol Chem. 2001;276:41059–41063
- Mutations in a member of the ADAMTS gene family cause thrombotic thrombocytopenic purpura. Nature. 2001;413:488–494
-
A novel human metalloprotease synthesized in the liver and secreted into the blood (Possibly, the von Willebrand factor-cleaving protease).
J Biochem (Tokyo). 2001;130:475–480
- Cloning, expression, and functional characterization of the von Willebrand factor-cleaving protease (ADAMTS13). Blood. 2002;100:3626–3632
- . Congenital deficiency of a factor in normal plasma that reverses microangiopathic hemolysis and thrombocytopenia. N Engl J Med. 1978;298:1350–1352
- . Studies on thrombopoiesis. I: A factor in normal human plasma required for platelet production; chronic thrombocytopenia due to its deficiency. Blood. 1960;16:943–957
-
Mutations and common polymorphisms in ADAMTS13 gene responsible for von Willebrand factor-cleaving protease activity.
Proc Natl Acad Sci USA. 2002;99:11902–11907
- Von Willebrand factor cleaving protease and ADAMTS13 mutations in childhood TTP. Blood. 2003;101:1845–1850
- ADAMTS13 gene defects in two brothers with constitutional thrombotic thrombocytopenic purpura and normalization of von Willebrand factor-cleaving protease activity by recombinant human ADAMTS13. Br J Haematol. 2003;120:821–824
- . ADAMTS13 gene mutation in congenital thrombotic thrombocytopenic purpura with previously reported normal VWF cleaving protease activity. Blood. 2003;101:4449–4451
- Mutation analysis and clinical implications of von Willebrand factor-cleaving protease deficiency. Kidney Int. 2003;63:1995–1999
-
.
Thrombotic thrombocytopenic purpura (Report of 16 cases and review of the literature).
Medicine (Baltimore). 1966;45:139–159
- Comparison of plasma exchange with plasma infusion in the treatment of thrombotic thrombocytopenic purpura. Canadian Apheresis Study Group. N Engl J Med. 1991;325:393–397
- . Treatment of thrombotic thrombopenic purpura. Results of a multicenter randomized clinical study. Presse Med. 1991;20:1761–1767
- . Improved survival in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Clinical experience in 108 patients. N Engl J Med. 1991;325:398–403
- . How I treat patients with thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Blood. 2000;96:1223–1229
- . Guidelines on the diagnosis and management of the thrombotic microangiopathic haemolytic anaemias. Br J Haematol. 2003;120:556–573
- . Hämolytisch-urämische Syndrome (Bilaterale Nierenrindennekrosen bei akuten erworbenen hämolytischen Anämien). Schweiz Med Wochenschr. 1955;85:905–909
- . Effectiveness of therapeutic plasma exchange in the 1996 Lanarkshire Escherichia coli O157:H7 outbreak. Lancet. 1999;354:1327–1330
- . Thrombotic microangiopathy, hemolytic uremic syndrome, and thrombotic thrombocytopenic purpura. Kidney Int. 2001;60:831–846
- ADAMTS13 activity in thrombotic thrombocytopenic purpura-hemolytic uremic syndrome (relation to presenting features and clinical outcomes in a prospective cohort of 142 patients). Blood. 2003;102:60–68
- . Von Willebrand factor-cleaving protease (ADAMTS13) in thrombocytopenic disorders (A severely deficient activity is specific for thrombotic thrombocytopenic purpura). Blood. 2002;100:710–713
- Upshaw-Schulman syndrome revisited (A concept of congenital thrombotic thrombocytopenic purpura). Int J Hematol. 2001;74:101–108
- . Von Willebrand factor-cleaving protease (ADAMTS-13) activity in thrombotic microangiopathies (Diagnostic experience 2001/2002 of a single research laboratory). Swiss Med Wkly. 2003;133:325–332
- . Measurement of von Willebrand factor-cleaving protease (ADAMTS-13) activity in plasma (A multicenter comparison of different assay methods). J Thromb Haemost. 2003;1:1882–1887
- . Carcinoma-associated hemolytic-uremic syndrome (A complication of mitomycin C chemotherapy). J Clin Oncol. 1985;3:723–734
- . Thrombotic microangiopathy manifesting as thrombotic thrombocytopenic purpura/hemolytic uremic syndrome in the cancer patient. Semin Thromb Hemost. 1999;25:217–221
- . Drug-associated thrombotic thrombocytopenic purpura-hemolytic uremic syndrome. Curr Opin Hematol. 2001;8:286–293
- von Willebrand factor proteolysis is deficient in classic, but not in bone marrow transplantation-associated, thrombotic thrombocytopenic purpura. Blood. 1999;93:3798–3802
- von Willebrand factor and von Willebrand factor-cleaving metalloprotease activity in Escherichia coli O157:H7-associated hemolytic uremic syndrome. Pediatr Res. 2001;49:653–659
-
Predicting response to plasma exchange in patients with thrombotic thrombocytopenic purpura with measurement of vWF-cleaving protease activity.
Transfusion. 2002;42:572–580
- Posttransplantation thrombotic thrombocytopenic purpura (A single-center experience and a contemporary review). Mayo Clin Proc. 2003;78:421–430
- . von Willebrand factor-cleaving protease in childhood diarrhoea-associated haemolytic uraemic syndrome. Thromb Haemost. 2001;85:975–978
- . Specific von Willebrand factor-cleaving protease in thrombotic microangiopathies (A study of 111 cases). Blood. 2001;98:1765–1772
- Severe deficiency of the specific von Willebrand factor-cleaving protease (ADAMTS 13) activity in a subgroup of children with atypical hemolytic uremic syndrome. J Pediatr. 2003;142:310–317
- von Willebrand factor cleaving protease (ADAMTS13) is deficient in recurrent and familial thrombotic thrombocytopenic purpura and hemolytic uremic syndrome. Blood. 2002;100:778–785
- . Is ADAMTS-13 deficiency specific for thrombotic thrombocytopenic purpura? No. J Thromb Haemost. 2003;1:632–634
- . Is severe deficiency of ADAMTS-13 specific for thrombotic thrombocytopenic purpura? Yes. J Thromb Haemost. 2003;1:625–631
- . Low activity of von Willebrand factor-cleaving protease is not restricted to patients suffering from thrombotic thrombocytopenic purpura. Br J Haematol. 2001;112:1087–1088
- . Decreased von Willebrand factor protease activity associated with thrombocytopenic disorders. Blood. 2001;98:1842–1846
- . Aetiology and pathogenesis of thrombotic thrombocytopenic purpura and haemolytic uraemic syndrome (The role of von Willebrand factor-cleaving protease). Best Pract Res Clin Haematol. 2001;14:437–454
- . Anti-CD36 antibodies in thrombotic thrombocytopenic purpura. Br J Haematol. 1994;88:816–825
- Anti-CD36 autoantibodies in thrombotic thrombocytopenic purpura and other thrombotic disorders (Identification of an 85 kD form of CD36 as a target antigen). Br J Haematol. 1998;103:849–857
- ADAMTS-13 rapidly cleaves newly secreted ultralarge von Willebrand factor multimers on the endothelial surface under flowing conditions. Blood. 2002;100:4033–4039
- . Late relapses in patients successfully treated for thrombotic thrombocytopenic purpura. Canadian Apheresis Group. Ann Intern Med. 1995;122:569–572
- . Thrombotic thrombocytopenic purpura in 13 Dutch centres (Treatment and longterm follow-up). Ned Tijdschr Geneeskd. 1997;141:1192–1196
-
.
Remission of chronic thrombotic thrombocytopenic purpura after treatment with cyclophosphamide and rituximab.
Ann Intern Med. 2003;138:105–108
-
Non-neutralizing IgM and IgG antibodies to von Willebrand factor-cleaving protease (ADAMTS-13) in a patient with thrombotic thrombocytopenic purpura (TTP).
Blood. 2003;
DOI 10.1182/blood-2003-05-1616
-
.
Platelets (Thrombotic thrombocytopenic purpura).
Hematology (Am Soc Hematol Educ Program). 2002;315–334
☆ Supported by a grant from the Swiss National Foundation for Scientific Research (32-66756.01).
PII: S0037-1963(03)00281-6
doi: 10.1053/j.seminhematol.2003.10.008
© 2004 Elsevier Inc. All rights reserved.
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Seminars in Hematology
Volume 41, Issue 1
, Pages 75-82
, January 2004
