Literature DB >> 29446525

Laboratory testing for factor VIII and IX inhibitors in haemophilia: A review.

C H Miller1.   

Abstract

Inhibitors are antibodies directed against haemophilia treatment products which interfere with their function. Factor VIII (FVIII) inhibitors in haemophilia A and factor IX (FIX) inhibitors in haemophilia B are significant clinically when they require a change in a patient's treatment regimen. Their persistence may increase morbidity and mortality. Multiple laboratory tests are now available for detecting and understanding inhibitors in haemophilia. Inhibitors are traditionally measured by their interference in clotting or chromogenic factor assays. They may also be detected using immunologic assays, such as enzyme-linked immunosorbent assay or fluorescence immunoassay. Anti-FVIII or anti-FIX antibodies of IgG4 subclass best correlate with the presence of functional inhibitors. Improvements in inhibitor measurement have been recently introduced. Preanalytical heat treatment of patient specimens allows testing of patients without delaying treatment. Use of chromogenic and immunologic assays may aid in identification of false-positive results, which are frequent among low-titre inhibitors. Validated reagent substitutions can be used to reduce assay cost. New methods for defining assay positivity and reporting low-titre inhibitors have been suggested. Challenges remain in the areas of quality control, assay standardization, monitoring of patients undergoing immune tolerance induction therapy and testing in the presence of modified and novel treatment products. Published 2018. This article is a U.S. Government work and is in the public domain in the USA.

Entities:  

Keywords:  factor IX; factor VIII; haemophilia; inhibitor

Mesh:

Substances:

Year:  2018        PMID: 29446525      PMCID: PMC6033270          DOI: 10.1111/hae.13424

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


  92 in total

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2.  Lupus anticoagulants associated inhibitor against factor IX in a young patient with haemophilia B.

Authors:  A Barnbrock; C Heller; C Königs; U Budde; D Schwabe
Journal:  Haemophilia       Date:  2016-06-28       Impact factor: 4.287

Review 3.  Acquired haemophilia A: a 2013 update.

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Journal:  Thromb Haemost       Date:  2013-09-05       Impact factor: 5.249

4.  Limit of detection and threshold for positivity of the Centers for Disease Control and Prevention assay for factor VIII inhibitors.

Authors:  C H Miller; B Boylan; A D Shapiro; S R Lentz; B M Wicklund
Journal:  J Thromb Haemost       Date:  2017-09-14       Impact factor: 5.824

5.  Physical functioning in boys with hemophilia in the U.S.

Authors:  Paul E Monahan; Judith R Baker; Brenda Riske; J Michael Soucie
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6.  Does the presence of von Willebrand factor in FVIII-deficient plasma influences the measurement of FVIII inhibitor titres in haemophilia A patients?

Authors:  C Pouplard; C Desconclois; F Sobas; M F Aillaud; C Ternisien; C Caron
Journal:  Int J Lab Hematol       Date:  2014-05-12       Impact factor: 2.877

7.  The EPIC study: a lesson to learn.

Authors:  G Auerswald; K Kurnik; L M Aledort; H Chehadeh; A Loew-Baselli; K Steinitz; A J Reininger
Journal:  Haemophilia       Date:  2015-04-23       Impact factor: 4.287

8.  Inhibitors in factor IX deficiency a report of the ISTH-SSC international FIX inhibitor registry (1997-2006).

Authors:  M Chitlur; I Warrier; M Rajpurkar; J M Lusher
Journal:  Haemophilia       Date:  2009-06-10       Impact factor: 4.287

9.  Distinct characteristics of antibody responses against factor VIII in healthy individuals and in different cohorts of hemophilia A patients.

Authors:  Shawn F J Whelan; Christoph J Hofbauer; Frank M Horling; Peter Allacher; Martin J Wolfsegger; Johannes Oldenburg; Christoph Male; Jerzy Windyga; Andreas Tiede; Hans Peter Schwarz; Friedrich Scheiflinger; Birgit M Reipert
Journal:  Blood       Date:  2012-12-12       Impact factor: 22.113

10.  Spontaneous disappearance of an IgA anti-factor IX inhibitor in a child with Christmas disease.

Authors:  R R Carroll; R S Panush; C S Kitchens
Journal:  Am J Hematol       Date:  1984-10       Impact factor: 10.047

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  10 in total

Review 1.  Experience of Immune Tolerance Induction Therapy for Hemophilia A Patients with Inhibitors from a Single Center in India.

Authors:  Tulika Seth
Journal:  Indian J Hematol Blood Transfus       Date:  2019-11-04       Impact factor: 0.900

2.  Reagent substitution in the chromogenic Bethesda assay for factor VIII inhibitors.

Authors:  Amanda B Payne; Connie H Miller; Dorothy Ellingsen; Jennifer Driggers; Brian Boylan; Christopher J Bean
Journal:  Haemophilia       Date:  2019-07-29       Impact factor: 4.287

3.  Management of rare acquired bleeding disorders.

Authors:  Marzia Menegatti; Eugenia Biguzzi; Flora Peyvandi
Journal:  Hematology Am Soc Hematol Educ Program       Date:  2019-12-06

Review 4.  Consensus recommendations on appropriate coagulation tests during emicizumab administration in Saudi Arabia.

Authors:  Tarek Owaidah; Abdulakareem Almomen; Ahmed Tarawah; Ashraf Warsi; Fawaz Alkasim; Hazzaa Alzahrani; Mahassen Saleh; Ohoud Kashari; Wasil Jastaniah
Journal:  Am J Blood Res       Date:  2022-06-20

5.  Validation of the chromogenic Bethesda assay for factor VIII inhibitors in hemophilia a patients receiving Emicizumab.

Authors:  Connie H Miller; Brian Boylan; Amanda B Payne; Jennifer Driggers; Christopher J Bean
Journal:  Int J Lab Hematol       Date:  2020-11-10       Impact factor: 2.877

6.  Navigating Speed Bumps on the Innovation Highway in Hemophilia Therapeutics.

Authors:  Donna M DiMichele
Journal:  Hemasphere       Date:  2018-10-02

7.  Safety and efficacy of turoctocog alfa in the prevention and treatment of bleeds in previously untreated paediatric patients with severe haemophilia A: Results from the guardian 4 multinational clinical trial.

Authors:  Hassan Yaish; Tadashi Matsushita; Meriem Belhani; Víctor Jiménez-Yuste; Kaan Kavakli; Lars Korsholm; Irina Matytsina; Claire Philipp; Kirsten Reichwald; Runhui Wu
Journal:  Haemophilia       Date:  2019-12-09       Impact factor: 4.287

8.  Emicizumab in tolerized patients with hemophilia A with inhibitors: A single-institution pediatric cohort assessing inhibitor status.

Authors:  Glaivy Batsuli; Amanda Greene; Shannon L Meeks; Robert F Sidonio
Journal:  Res Pract Thromb Haemost       Date:  2021-02-08

Review 9.  Acquired hemophilia A (AHA): underreported, underdiagnosed, undertreated medical condition.

Authors:  Doaa M El Demerdash; Alia Ayad; Noha Tawfik
Journal:  Egypt J Intern Med       Date:  2022-01-25

10.  Evaluation of nonneutralizing antibodies against factor VIII in severe haemophilia A patients from India.

Authors:  Sachin David; Nitty S Mathews; G Surender Singh; Anu Korula; Fouzia Nambiatheyil Aboobacker; Aby Abraham; Biju George; Alok Srivastava; Vikram Mathews; Sukesh C Nair
Journal:  Blood Coagul Fibrinolysis       Date:  2019-10       Impact factor: 1.276

  10 in total

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