Literature DB >> 15827129

Rituximab prevents recurrence of thrombotic thrombocytopenic purpura: a case report.

Miriam Galbusera1, Elena Bresin, Marina Noris, Sara Gastoldi, Daniela Belotti, Cristina Capoferri, Erica Daina, Paolo Perseghin, Friedrich Scheiflinger, Fadi Fakhouri, Jean-Pierre Grünfeld, Enrico Pogliani, Giuseppe Remuzzi.   

Abstract

Thrombotic thrombocytopenic purpura (TTP) is a rare disorder of small vessels that is associated with deficiency of the von Willebrand factor-cleaving protease, ADAMTS13. The presence of anti-ADAMTS13 autoantibodies is considered a factor predisposing to relapses. Despite close monitoring and intensive plasma treatment, in these patients acute episodes are still associated with substantial morbidity and mortality rates, and the optimal therapeutic option should be prevention of relapses. This study was conducted in a patient with recurrent TTP due to high titers of ADAMTS13 inhibitors, who used to have 2 relapses of TTP a year. The study compared the standard treatment plasma exchange with rituximab. Results documented that plasma exchange had only a small transient effect on ADAMTS13 activity and inhibitors; on the contrary, prophylaxis with rituximab was associated with disappearance of anti-ADAMTS13 antibodies, a progressive recovery of protease activity, and it allowed the patient to maintain a disease-free state during a more than 2-year follow-up.

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Year:  2005        PMID: 15827129     DOI: 10.1182/blood-2004-12-4885

Source DB:  PubMed          Journal:  Blood        ISSN: 0006-4971            Impact factor:   22.113


  8 in total

1.  A dramatic response to rituximab in a patient with resistant thrombotic thrombocytopenic purpura (TTP) who developed acute stroke.

Authors:  Hakan Ozdogu; Can Boga; Ebru Kizilkilic; Mahmut Yeral; Ilknur Kozanoglu; Mehmet Karatas
Journal:  J Thromb Thrombolysis       Date:  2007-01-13       Impact factor: 2.300

Review 2.  The role of rituximab in the management of patients with acquired thrombotic thrombocytopenic purpura.

Authors:  Wendy Lim; Sara K Vesely; James N George
Journal:  Blood       Date:  2015-01-08       Impact factor: 22.113

Review 3.  Translational mini-review series on complement factor H: therapies of renal diseases associated with complement factor H abnormalities: atypical haemolytic uraemic syndrome and membranoproliferative glomerulonephritis.

Authors:  M Noris; G Remuzzi
Journal:  Clin Exp Immunol       Date:  2007-12-07       Impact factor: 4.330

Review 4.  Von Willebrand factor, ADAMTS13, and thrombotic thrombocytopenic purpura.

Authors:  J Evan Sadler
Journal:  Blood       Date:  2008-07-01       Impact factor: 22.113

5.  Idiopathic Relapsing Thrombotic Thrombocytopenic Purpura with Persistent ADAMTS13 Inhibitor Activity Treated Sequentially with Plasmapheresis, Rituximab, Cyclophosphamide and Splenectomy.

Authors:  Faisal Musa; Said Baidas
Journal:  Case Rep Oncol       Date:  2015-04-22

Review 6.  Management of acquired, immune thrombocytopenic purpura (iTTP): beyond the acute phase.

Authors:  John Paul Westwood; Marie Scully
Journal:  Ther Adv Hematol       Date:  2022-07-26

7.  Efficacy and Safety of Rituximab for Refractory and Relapsing Thrombotic Thrombocytopenic Purpura: A Cohort of 10 Cases.

Authors:  Halima El Omri; Ruba Y Taha; Amna Gamil; Firyal Ibrahim; Hisham Al Sabah; Zeinab O Mahmoud; Gianfranco Pittari; Ibrahim Al HIjji; Mohamed A Yassin
Journal:  Clin Med Insights Blood Disord       Date:  2015-05-24

8.  ADAMTS13 predicts renal and cardiovascular events in type 2 diabetic patients and response to therapy.

Authors:  Erica Rurali; Marina Noris; Antonietta Chianca; Roberta Donadelli; Federica Banterla; Miriam Galbusera; Giulia Gherardi; Sara Gastoldi; Aneliya Parvanova; Ilian Iliev; Antonio Bossi; Carolina Haefliger; Roberto Trevisan; Giuseppe Remuzzi; Piero Ruggenenti
Journal:  Diabetes       Date:  2013-06-03       Impact factor: 9.461

  8 in total

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