Plasma proteomics associated with autoimmune coagulation factor deficiencies reveals the link between inflammation and autoantibody development
Author:
Funder
Ministry of Education, Culture, Sports, Science and Technology
The Japanese Ministry of Health, Labor and Welfare
Publisher
Springer Science and Business Media LLC
Subject
Hematology
Link
https://link.springer.com/content/pdf/10.1007/s12185-022-03301-3.pdf
Reference32 articles.
1. Ichinose A. Japanese Collaborative Research Group on AH13. Autoimmune acquired factor XIII deficiency due to anti-factor XIII/13 antibodies: a summary of 93 patients. Blood Rev. 2017;31:37–45.
2. Ichinose A, Souri M. Reduced difference of α2-plasmin inhibitor levels between plasma and serum in patients with severe factor FXIII deficiency, including autoimmune haemorrhaphilia due to anti-factor XIII antibodies. Int J Hematol. 2012;95:47–50.
3. Kruse-Jarres R, Kempton CL, Baudo F, Collins PW, Knoebl P, Leissinger CA, et al. Acquired hemophilia A: updated review of evidence and treatment guidance. Am J Hematol. 2017;92:695–705.
4. Ogawa H, Souri M, Kanouchi K, Osaki T, Ohkubo R, Kawanishi T, et al. A high titer of acquired factor V inhibitor in a hemodialysis patient who developed arterial thrombosis. Int J Hematol. 2019;109:214–20.
5. Oldenburg J, Zeitler H, Pavlova A. Genetic markers in acquired haemophilia. Haemophilia. 2010;16:41–5.
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2. Diagnosis and Treatment of Autoimmune Acquired Coagulation Factor Deficiencies: An Evidence-Based Review of Japanese Practice;Seminars in Thrombosis and Hemostasis;2024-06-12
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