Literature DB >> 27439658

Joint bleeds increase the inhibitor response to human factor VIII in a rat model of severe haemophilia A.

K M Lövgren1,2, H Søndergaard3, S Skov4, B Wiinberg5.   

Abstract

INTRODUCTION: The most serious complication in haemophilia A (HA) replacement therapy with coagulation factor VIII (FVIII) is neutralizing antibodies, i.e. inhibitors. It has been hypothesized that danger signals generated during a bleed might have an adjuvant effect on the immune response to FVIII in on-demand treatment, increasing the inhibitor risk. AIM: To compare the antibody response to treatment with recombinant human FVIII (rhFVIII) in relation to induced knee joint bleeds and treatment without concurrent bleeds in a HA rat model.
METHOD: HA rats were divided into two groups: one group (n = 10) receiving three needle induced knee joint bleeds 14 days apart and a control group (n = 9) receiving three sham procedures. Three hours after each injury/sham 50 IU kg(-1) rhFVIII was administrated intravenously. Subsequently, both groups continued rhFVIII treatment for another 9 weeks. Binding antibodies were analysed using an enzyme-linked immunosorbent assay and neutralizing antibodies using a Bethesda-like assay.
RESULTS: Rats in the knee-bleed group developed a significantly faster inhibitor response and reached significantly higher inhibitor levels. In the knee-bleed group, 80% developed inhibitors vs. 33% in the control group, demonstrating a 2.4 times higher inhibitor risk when treating concurrent with bleeds.
CONCLUSION: FVIII treatment in relation to a bleed potentiates inhibitor development compared to FVIII treatment alone in this HA rat, indicating that bleeding is a potential danger signal. Our results support the theory that FVIII replacement therapy concurrent with a bleeding episode increases the inhibitor risk, which to the best of our knowledge, has not been confirmed in an animal model before.
© 2016 John Wiley & Sons Ltd.

Entities:  

Keywords:  animal model; factor VIII; haemarthrosis; haemophilia A; inhibitors; rats

Mesh:

Substances:

Year:  2016        PMID: 27439658     DOI: 10.1111/hae.13014

Source DB:  PubMed          Journal:  Haemophilia        ISSN: 1351-8216            Impact factor:   4.287


  3 in total

1.  Dexamethasone promotes durable factor VIII-specific tolerance in hemophilia A mice via thymic mechanisms.

Authors:  Maria T Georgescu; Paul C Moorehead; Alice S van Velzen; Kate Nesbitt; Birgit M Reipert; Katharina N Steinitz; Maria Schuster; Christine Hough; David Lillicrap
Journal:  Haematologica       Date:  2018-04-19       Impact factor: 9.941

2.  Serum TNF-α Level as a Possible Predictor of Inhibitor Levels in Severe Hemophilia A.

Authors:  Susi Susanah; Harry Raspati; Nur Melani Sari; Lulu Eva Rakhmilla; Yunia Sribudiani; Octawyana Moestopo; Puspasari Sinaga; Ponpon Idjradinata; Ani Melani Maskoen
Journal:  Biomed Res Int       Date:  2021-11-05       Impact factor: 3.411

3.  Sedimentation Velocity Analytical Ultracentrifugation of Oxidized Recombinant Full-Length Factor VIII.

Authors:  Philip M Zakas; John F Healey; Ian W Smith; David Lillicrap; Pete Lollar
Journal:  Front Immunol       Date:  2020-02-07       Impact factor: 7.561

  3 in total

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