Rituximab can be combined with daily plasma exchange to achieve effective B-cell depletion and clinical improvement in acute autoimmune TTP

K Darabi, AH Berg - American journal of clinical pathology, 2006 - academic.oup.com
K Darabi, AH Berg
American journal of clinical pathology, 2006academic.oup.com
Much of idiopathic thrombotic thrombocytopenic purpura (TTP) is attributed to the presence
of an autoantibody to ADAMTS-13, the metalloprotease that degrades ultralarge von
Willebrand protein multimers. Most patients respond to treatment with therapeutic plasma
exchange (TPE), which replaces the missing protease and removes the circulating inhibitor.
However, a substantial fraction of idiopathic TTP cases (10%-20%) might not respond to
TPE alone, and, therefore, interest has been gathering around the use of the novel …
Abstract
Much of idiopathic thrombotic thrombocytopenic purpura (TTP) is attributed to the presence of an autoantibody to ADAMTS-13, the metalloprotease that degrades ultralarge von Willebrand protein multimers. Most patients respond to treatment with therapeutic plasma exchange (TPE), which replaces the missing protease and removes the circulating inhibitor. However, a substantial fraction of idiopathic TTP cases (10%-20%) might not respond to TPE alone, and, therefore, interest has been gathering around the use of the novel immunosuppressive anti–B-cell antibody, rituximab. We report 2 cases of refractory TTP in which the combined use of daily plasma exchange and rituximab was associated with clinical resolution of active TTP, and we discuss the benefits and possible timing of combined therapy.
Oxford University Press