Assessing thrombogenesis and treatment response in congenital thrombotic thrombocytopenic purpura.

Ferras Alwan, Chiara Vendramin, Ulrich Budde, Ri Liesner, Alice Taylor, Mari Thomas, Bernhard L��mmle, Marie Scully
Author Information
  1. Ferras Alwan: Department of Haematology University College London Hospital London UK. ORCID
  2. Chiara Vendramin: Department of Haematology University College London Hospital London UK.
  3. Ulrich Budde: Medilys Laboratory Coagulation Asklepios Hospital Altona Hamburg Germany.
  4. Ri Liesner: Haemophilia Comprehensive Care Centre Great Ormond Street Hospital for Children NHS Trust London UK.
  5. Alice Taylor: Haemophilia Comprehensive Care Centre Great Ormond Street Hospital for Children NHS Trust London UK.
  6. Mari Thomas: Department of Haematology University College London Hospital London UK.
  7. Bernhard L��mmle: Department of Hematology and Central Hematology Laboratory Inselspital Bern University Hospital University of Bern Bern Switzerland.
  8. Marie Scully: Department of Haematology University College London Hospital London UK. ORCID

Abstract

Despite clinical remission and normal platelet counts, congenital TTP (cTTP) is associated with non-overt symptoms. Prophylactic ADAMTS13 replacement therapy such as plasma infusion (PI) prevents acute episodes and improves symptomatology. There is no current method to investigate disease severity or monitor the impact of treatment. We utilize a dynamic high shear flow assay to further understand disease pathophysiology and determine the impact of cTTP on symptomatology and therapy, despite normal platelet counts. Whole blood, under high shear, was run over collagen-coated channels, causing platelet adhesion to von Willebrand factor (VWF) multimers. The resulting surface coverage by platelet-VWF thrombus was assessed. The normal range was 6-39% in 50 controls. Twenty-two cTTP patients with normal platelet counts were evaluated. Median pre-treatment surface coverage was 89%, and PI reduced coverage to a median of 44% ( = 0.0005). Patients taking antiplatelets had further reduced coverage when combined with PI and improved non-overt symptoms such as headache, lethargy, and abdominal pain in 100% of patients compared to 74% with PI alone ( = 0.046). We use a dynamic assay to report increased in vitro platelet adhesion and aggregation and additionally demonstrate significantly decreased thrombi following PI, with levels in the normal range levels achieved in patients taking additional antiplatelet therapy.

Keywords

References

  1. Thromb Res. 2017 Nov;159:91-95 [PMID: 29040872]
  2. Thromb Haemost. 1999 Jan;81(1):8-13 [PMID: 10348715]
  3. Thromb J. 2015 Feb 05;13:8 [PMID: 25688179]
  4. Br J Haematol. 2005 Apr;129(1):93-100 [PMID: 15801961]
  5. J Thromb Haemost. 2011 Nov;9(11):2322-4 [PMID: 22947397]
  6. Haemophilia. 2013 Mar;19(2):338-42 [PMID: 23205618]
  7. Br J Haematol. 2007 Feb;136(4):649-55 [PMID: 17367414]
  8. Blood. 2019 Apr 11;133(15):1644-1651 [PMID: 30770395]
  9. J Thromb Haemost. 2004 Apr;2(4):561-73 [PMID: 15102010]
  10. Transfusion. 2006 Aug;46(8):1444-52 [PMID: 16934083]
  11. BMC Nephrol. 2013 Jul 20;14:156 [PMID: 23870247]
  12. N Engl J Med. 2008 Aug 28;359(9):938-49 [PMID: 18753650]
  13. Hematology Am Soc Hematol Educ Program. 2012;2012:610-6 [PMID: 23233642]
  14. Blood. 2012 Jul 12;120(2):440-8 [PMID: 22529288]
  15. Sci Rep. 2016 Sep 26;6:33938 [PMID: 27666678]
  16. PLoS One. 2020 May 4;15(5):e0232637 [PMID: 32365113]
  17. N Engl J Med. 1982 Dec 2;307(23):1432-5 [PMID: 6813740]
  18. Semin Thromb Hemost. 2006 Mar;32(2):90-7 [PMID: 16575683]
  19. Br J Haematol. 2012 Aug;158(3):323-35 [PMID: 22624596]
  20. Thromb Res. 2014 Dec;134(6):1285-91 [PMID: 25201004]
  21. J Thromb Haemost. 2008 Feb;6(2):331-8 [PMID: 18031293]
  22. Br J Haematol. 2001 Jun;113(3):649-51 [PMID: 11380451]
  23. Blood. 2012 Jun 14;119(24):5888-97 [PMID: 22547583]
  24. J Thromb Haemost. 2019 Jan;17(1):88-98 [PMID: 30475428]
  25. Haematologica. 2019 Oct;104(10):2107-2115 [PMID: 30792199]
  26. Blood. 2017 Nov 9;130(19):2055-2063 [PMID: 28912376]
  27. Hamostaseologie. 2014;34(3):215-25 [PMID: 25010251]
  28. J Thromb Haemost. 2008 May;6(5):762-71 [PMID: 18315556]
  29. Semin Thromb Hemost. 2010 Feb;36(1):82-90 [PMID: 20391299]
  30. EJHaem. 2021 Feb 28;2(2):188-195 [PMID: 35845267]
  31. Blood. 2017 May 25;129(21):2836-2846 [PMID: 28416507]
  32. Blood. 2008 Sep 1;112(5):1713-9 [PMID: 18492952]

Word Cloud

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