Nonneutralizing FVIII-specific antibody signatures in patients with hemophilia A and in healthy donors.


Journal

Blood advances
ISSN: 2473-9537
Titre abrégé: Blood Adv
Pays: United States
ID NLM: 101698425

Informations de publication

Date de publication:
08 02 2022
Historique:
received: 13 07 2021
accepted: 29 10 2021
pubmed: 1 12 2021
medline: 12 4 2022
entrez: 30 11 2021
Statut: ppublish

Résumé

Previous studies identified nonneutralizing FVIII-specific antibodies in the circulation of severe and nonsevere hemophilia A (sHA and nsHA) patients without FVIII inhibitors and also in some healthy individuals. To gain a better understanding of the nature of these nonneutralizing antibody responses, we analyzed and compared anti-FVIII antibody signatures in 3 study cohorts: previously treated sHA as well as nsHA patients without FVIII inhibitors, and healthy donors. FVIII-binding IgM, IgG1-4, and IgA antibodies were differentiated, FVIII-specificity was assessed, and associated apparent affinity constants were determined. Our results indicate that the nonneutralizing FVIII-specific antibody response in all study cohorts is dominated by IgG1 and IgA. Prevalences, titers, and affinities of these nonneutralizing antibodies were higher in the hemophilia A cohorts than in healthy donors. Stratification for the anti-hepatitis C virus (HCV) antibody status demonstrated the presence of FVIII-specific IgA with elevated titers in sHA patients with an active or past HCV infection when compared with HCV antibody-positive nsHA patients or HCV antibody-negative patients and healthy donors. Increased titers and affinities of FVIII-specific IgG1 antibodies were observed in a considerable number of hemophilia A patients as opposed to healthy subjects independently of the patients' anti-HCV antibody status. Overall, our findings support the hypothesis that the generation of nonneutralizing anti-FVIII antibodies in healthy individuals and in noninhibitor hemophilia A patients might be based on similar immune mechanisms. However, differences in prevalences, titers, and affinities of these antibodies indicate distinct differences in the antibody evolution between healthy individuals and patients.

Identifiants

pubmed: 34847225
pii: 482837
doi: 10.1182/bloodadvances.2021005745
pmc: PMC8945293
doi:

Substances chimiques

Immunoglobulin A 0
Immunoglobulin G 0
Factor VIII 9001-27-8

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

946-958

Informations de copyright

© 2022 by The American Society of Hematology. Licensed under Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International (CC BY-NC-ND 4.0), permitting only noncommercial, nonderivative use with attribution. All other rights reserved.

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Auteurs

Helmut Schweiger (H)

Institute Krems Bioanalytics, IMC University of Applied Sciences Krems, Krems, Austria.

Judit Rejtő (J)

Clinical Division of Haematology and Haemostaseology, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria.

Christoph J Hofbauer (CJ)

Drug Discovery Austria, Baxalta Innovations GmbH, a member of the Takeda group of companies, Vienna, Austria.

Verena Berg (V)

Institute Krems Bioanalytics, IMC University of Applied Sciences Krems, Krems, Austria.

Peter Allacher (P)

Institute Krems Bioanalytics, IMC University of Applied Sciences Krems, Krems, Austria.

Karl Zwiauer (K)

Clinical Division of Pediatrics, University Hospital St. Pölten, St. Pölten, Austria.

Clemens Feistritzer (C)

Department of Internal Medicine V - Haematology and Oncology, Medical University of Innsbruck, Innsbruck, Austria; and.

Gerhard Schuster (G)

Upper Austrian Red Cross, Linz, Austria.

Cihan Ay (C)

Clinical Division of Haematology and Haemostaseology, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria.

Birgit M Reipert (BM)

Institute Krems Bioanalytics, IMC University of Applied Sciences Krems, Krems, Austria.
Drug Discovery Austria, Baxalta Innovations GmbH, a member of the Takeda group of companies, Vienna, Austria.

Ingrid Pabinger (I)

Clinical Division of Haematology and Haemostaseology, Department of Internal Medicine I, Medical University of Vienna, Vienna, Austria.

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