Factor VIII-Fc Activates Natural Killer Cells


Journal

Frontiers in immunology
ISSN: 1664-3224
Titre abrégé: Front Immunol
Pays: Switzerland
ID NLM: 101560960

Informations de publication

Date de publication:
2021
Historique:
received: 07 04 2021
accepted: 16 06 2021
entrez: 15 7 2021
pubmed: 16 7 2021
medline: 26 10 2021
Statut: epublish

Résumé

The most challenging complication associated with Factor VIII (FVIII) replacement therapy is the development of neutralizing anti-drug antibodies, or inhibitors, which occur in 23-35% of severe (FVIII level <1%) hemophilia A (HA) patients and are a serious hindrance to effective management of HA. Consequently, strategies that can either prevent anti-FVIII inhibitors from developing or "tolerize" individuals who develop such antibodies represent a clinically important unmet need. One intervention for patients with high-titer inhibitors is immune tolerance induction (ITI) therapy. Although ITI therapy is the only clinically proven strategy to eradicate anti-FVIII inhibitors, mechanisms of inhibitor reduction remain unknown. Factor VIII Fc-fusion (rFVIIIFc) is an enhanced half-life antihemophilic factor used in replacement therapy for HA. Fc-fusion is a successful protein bio-engineering platform technology. In addition to enhancement of plasma half-life

Identifiants

pubmed: 34262568
doi: 10.3389/fimmu.2021.692157
pmc: PMC8273617
doi:

Substances chimiques

FCGR3B protein, human 0
GPI-Linked Proteins 0
Hemostatics 0
Immunoglobulin Fc Fragments 0
Receptors, IgG 0
Recombinant Fusion Proteins 0
factor VIII-Fc fusion protein 0
Interferon-gamma 82115-62-6
Factor VIII 9001-27-8

Types de publication

Journal Article Research Support, U.S. Gov't, P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

692157

Informations de copyright

Copyright © 2021 Lagassé, Hopkins, Jankowski, Jacquemin, Sauna and Golding.

Déclaration de conflit d'intérêts

MJ reports grants from Bayer, Takeda, Pfizer and Sobi, outside the submitted work. The remaining authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.

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Auteurs

H A Daniel Lagassé (HAD)

Hemostasis Branch, Division of Plasma Protein Therapeutics, Office of Tissues and Advanced Therapies, Center for Biologics Evaluation and Research, Food and Drug Administration, Silver Spring, MD, United States.

Louis B Hopkins (LB)

Hemostasis Branch, Division of Plasma Protein Therapeutics, Office of Tissues and Advanced Therapies, Center for Biologics Evaluation and Research, Food and Drug Administration, Silver Spring, MD, United States.

Wojciech Jankowski (W)

Hemostasis Branch, Division of Plasma Protein Therapeutics, Office of Tissues and Advanced Therapies, Center for Biologics Evaluation and Research, Food and Drug Administration, Silver Spring, MD, United States.

Marc G Jacquemin (MG)

Department of Cardiovascular Sciences, Center for Molecular and Vascular Biology, University of Leuven, Leuven, Belgium.

Zuben E Sauna (ZE)

Hemostasis Branch, Division of Plasma Protein Therapeutics, Office of Tissues and Advanced Therapies, Center for Biologics Evaluation and Research, Food and Drug Administration, Silver Spring, MD, United States.

Basil Golding (B)

Hemostasis Branch, Division of Plasma Protein Therapeutics, Office of Tissues and Advanced Therapies, Center for Biologics Evaluation and Research, Food and Drug Administration, Silver Spring, MD, United States.

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