Literature DB >> 16409158

Current concepts in thrombotic thrombocytopenic purpura.

Han-Mou Tsai1.   

Abstract

Recent advances have demonstrated that thrombotic thrombocytopenic purpura (TTP), characterized by widespread thrombosis in the arterioles and capillaries, is caused by deficiency of a circulating zinc metalloprotease, ADAMTS13. Two types of TTP are recognized: autoimmune TTP, caused by inhibitory antibodies of ADAMTS13, and hereditary TTP, caused by genetic mutations of ADAMTS13. This article reviews the characteristics and function of ADAMTS13, the mechanism by which ADAMTS13 deficiency may lead to thrombosis, and the causes of ADAMTS13 deficiency. It also discusses how the new knowledge may improve the diagnosis and treatment of this previously mysterious disorder.

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Year:  2006        PMID: 16409158      PMCID: PMC2426955          DOI: 10.1146/annurev.med.57.061804.084505

Source DB:  PubMed          Journal:  Annu Rev Med        ISSN: 0066-4219            Impact factor:   13.739


  70 in total

1.  Ultralarge von Willebrand factor multimers and normal ADAMTS13 activity in the umbilical cord blood.

Authors:  Han-Mou Tsai; Ravindra Sarode; Katharine A Downes
Journal:  Thromb Res       Date:  2002-11-01       Impact factor: 3.944

2.  Rituximab induces remission of cerebral ischemia caused by thrombotic thrombocytopenic purpura.

Authors:  Han-Mou Tsai; Keith Shulman
Journal:  Eur J Haematol       Date:  2003-03       Impact factor: 2.997

3.  Cleavage of the ADAMTS13 propeptide is not required for protease activity.

Authors:  Elaine M Majerus; Xinglong Zheng; Elodee A Tuley; J Evan Sadler
Journal:  J Biol Chem       Date:  2003-09-15       Impact factor: 5.157

4.  Transplantation-associated thrombotic microangiopathy is associated with transplantation from unrelated donors, acute graft-versus-host disease and venoocclusive disease of the liver.

Authors:  Andrew S Daly; Wanda S Hasegawa; Jeffrey H Lipton; Hans A Messner; Thomas L Kiss
Journal:  Transfus Apher Sci       Date:  2002-08       Impact factor: 1.764

5.  ADAMTS-13 cysteine-rich/spacer domains are functionally essential for von Willebrand factor cleavage.

Authors:  Kenji Soejima; Masanori Matsumoto; Koichi Kokame; Hideo Yagi; Hiromichi Ishizashi; Hiroaki Maeda; Chikateru Nozaki; Toshiyuki Miyata; Yoshihiro Fujimura; Tomohiro Nakagaki
Journal:  Blood       Date:  2003-07-17       Impact factor: 22.113

6.  Nonneutralizing IgM and IgG antibodies to von Willebrand factor-cleaving protease (ADAMTS-13) in a patient with thrombotic thrombocytopenic purpura.

Authors:  Friedrich Scheiflinger; Paul Knöbl; Bettina Trattner; Barbara Plaimauer; Gabriele Mohr; Michael Dockal; Friedrich Dorner; Manfred Rieger
Journal:  Blood       Date:  2003-07-10       Impact factor: 22.113

Review 7.  Genetic defects leading to hereditary thrombotic thrombocytopenic purpura.

Authors:  Koichi Kokame; Toshiyuki Miyata
Journal:  Semin Hematol       Date:  2004-01       Impact factor: 3.851

8.  Von Willebrand factor-cleaving protease (ADAMTS13) in thrombocytopenic disorders: a severely deficient activity is specific for thrombotic thrombocytopenic purpura.

Authors:  Valentina Bianchi; Rodolfo Robles; Lorenzo Alberio; Miha Furlan; Bernhard Lämmle
Journal:  Blood       Date:  2002-07-15       Impact factor: 22.113

9.  Thrombotic thrombocytopenic purpura in a newborn.

Authors:  Paul T Jubinsky; Richard Moraille; Han-Mou Tsai
Journal:  J Perinatol       Date:  2003-01       Impact factor: 2.521

10.  Changes in von Willebrand factor-cleaving protease (ADAMTS13) activity after infusion of desmopressin.

Authors:  Rosemarie A Reiter; Paul Knöbl; Katalin Varadi; Peter L Turecek
Journal:  Blood       Date:  2002-09-19       Impact factor: 22.113

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  24 in total

Review 1.  ADAMTS13 and microvascular thrombosis.

Authors:  Han-Mou Tsai
Journal:  Expert Rev Cardiovasc Ther       Date:  2006-11

Review 2.  Advantages and limits of ADAMTS13 testing in thrombotic thrombocytopenic purpura.

Authors:  Massimo Franchini; Pier Mannuccio Mannucci
Journal:  Blood Transfus       Date:  2008-07       Impact factor: 3.443

3.  Measurement of ADAMTS13.

Authors:  Han-Mou Tsai
Journal:  Int Rev Thromb       Date:  2006

4.  Shear stress-induced unfolding of VWF accelerates oxidation of key methionine residues in the A1A2A3 region.

Authors:  Xiaoyun Fu; Junmei Chen; Ryan Gallagher; Ying Zheng; Dominic W Chung; José A López
Journal:  Blood       Date:  2011-09-13       Impact factor: 22.113

5.  Cyclosporin A impairs the secretion and activity of ADAMTS13 (a disintegrin and metalloprotease with thrombospondin type 1 repeat).

Authors:  Klilah Hershko; Vijaya L Simhadri; Adam Blaisdell; Ryan C Hunt; Jordan Newell; Sandra C Tseng; Alon Y Hershko; Jae Won Choi; Zuben E Sauna; Andrew Wu; Richard J Bram; Anton A Komar; Chava Kimchi-Sarfaty
Journal:  J Biol Chem       Date:  2012-11-09       Impact factor: 5.157

6.  Formation and Resolution of Pial Microvascular Thrombosis in a Mouse Model of Thrombotic Thrombocytopenic Purpura.

Authors:  Reheman Adili; Michael Holinstat
Journal:  Arterioscler Thromb Vasc Biol       Date:  2019-07-25       Impact factor: 8.311

7.  Internal Tensile Force and A2 Domain Unfolding of von Willebrand Factor Multimers in Shear Flow.

Authors:  Michael Morabito; Chuqiao Dong; Wei Wei; Xuanhong Cheng; Xiaohui F Zhang; Alparslan Oztekin; Edmund Webb
Journal:  Biophys J       Date:  2018-09-13       Impact factor: 4.033

8.  N-Glycans of ADAMTS13 modulate its secretion and von Willebrand factor cleaving activity.

Authors:  Wenhua Zhou; Han-Mou Tsai
Journal:  Blood       Date:  2008-11-03       Impact factor: 22.113

9.  Multi-step binding of ADAMTS-13 to von Willebrand factor.

Authors:  H B Feys; P J Anderson; K Vanhoorelbeke; E M Majerus; J E Sadler
Journal:  J Thromb Haemost       Date:  2009-09-18       Impact factor: 5.824

Review 10.  Pathogenesis and prognosis of thrombotic microangiopathy.

Authors:  Masaomi Nangaku; Hiroshi Nishi; Toshiro Fujita
Journal:  Clin Exp Nephrol       Date:  2007-06-28       Impact factor: 2.801

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