Von Willebrand factor assays in patients with acquired immune thrombotic thrombocytopenia purpura treated with caplacizumab. (8th March 2022)
- Record Type:
- Journal Article
- Title:
- Von Willebrand factor assays in patients with acquired immune thrombotic thrombocytopenia purpura treated with caplacizumab. (8th March 2022)
- Main Title:
- Von Willebrand factor assays in patients with acquired immune thrombotic thrombocytopenia purpura treated with caplacizumab
- Authors:
- Bowyer, Annette
Brown, Paula
Hopkins, Barbara
Scully, Marie
Shepherd, Fiona
Lowe, Anna
Mensah, Patrick
Maclean, Rhona
Kitchen, Steve
van Veen, Joost J. - Abstract:
- Abstract: Acquired immune thrombotic thrombocytopenic purpura (iTTP) is a rare disease with a poor prognosis if undiagnosed. It is caused by autoantibody production to the von Willebrand factor (VWF) cleaving protease, A disintegrin and metalloproteinase with a thrombospondin type 1 motif, member 13 (ADAMTS13). Caplacizumab, an immunoglobulin directed to the platelet glycoprotein Ibα receptor of VWF, has been reported to induce quicker resolution of iTTP compared to placebo. The laboratory measurement of VWF activity was significantly reduced in clinical trials of caplacizumab. Several VWF assays are available in the UK and this study investigated whether differences in VWF parameters were present in 11 patients diagnosed with iTTP and treated with daily caplacizumab. Chromogenic factor VIII activity, VWF antigen, collagen binding activity, VWF multimers and six VWF activity assays were measured prior to caplacizumab therapy and on several occasions during treatment. VWF antigen and collagen binding activity levels were normal or borderline normal in all patients. Ultra‐large molecular weight multimers were present in all patients following treatment. VWF activity assays were normal or reduced during treatment, but this was reagent and patient dependant. In the unusual scenario of a caplacizumab‐treated patient requiring measurement of VWF activity, it is important that laboratories understand how their local reagents perform as results cannot be predicted.
- Is Part Of:
- British journal of haematology. Volume 197:Number 3(2022)
- Journal:
- British journal of haematology
- Issue:
- Volume 197:Number 3(2022)
- Issue Display:
- Volume 197, Issue 3 (2022)
- Year:
- 2022
- Volume:
- 197
- Issue:
- 3
- Issue Sort Value:
- 2022-0197-0003-0000
- Page Start:
- 349
- Page End:
- 358
- Publication Date:
- 2022-03-08
- Subjects:
- Acquired thrombotic thrombocytopenic purpura -- caplacizumab -- immune thrombotic thrombocytopenic purpura -- von Willebrand factor activity
Hematology -- Periodicals
Blood -- Diseases -- Periodicals
616.15 - Journal URLs:
- http://www.blacksci.co.uk/%7Ecgilib/jnlpage.bin?Journal=bjh&File=bjh&Page=aims ↗
http://onlinelibrary.wiley.com/journal/10.1111/(ISSN)1365-2141 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1111/bjh.18080 ↗
- Languages:
- English
- ISSNs:
- 0007-1048
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 2309.000000
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 21443.xml