ArticleAmerican journal of hematology2008
Evolution of ADAMTS13 antibodies in a fatal case of thrombotic thrombocytopenic purpura.
Article in American journal of hematology, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.
What it found
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
4 citing papers in PubMed.
- Weight loss reduces anti-ADAMTS13 autoantibodies and improves inflammatory and coagulative parameters in obese patients.Endocrine · 2017Article
- Proteolytic processing of von Willebrand factor by adamts13 and leukocyte proteases.Mediterranean journal of hematology and infectious diseases · 2013Review
- Pathophysiology of thrombotic thrombocytopenic purpura.International journal of hematology · 2010Review
- Mechanisms of microvascular thrombosis in thrombotic thrombocytopenic purpura.Kidney international. Supplement · 2009Review
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
In a patient with fatal thrombotic thrombocytopenic purpura, the inhibitory activity of antibodies against ADAMTS13 rapidly escalated to extremely high levels despite daily plasma exchange and corticosteroid therapy. This increase was found to be because of a combination of higher antibody concentration and potency. Furthermore, during her course of the disease, the percentage of IgG(1) antibody progressively decreased whereas that of IgG(2) antibody increased, suggesting Th1-type cytokine response. These changes suggest that the course of TTP may be exacerbated by complex immune reactions. Further characterization of the factors contributing to this exacerbation may have important pathogenetic and therapeutic implications.
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