Life in the shadow of a dominant partner: the FVIII-VWF association and its clinical implications for hemophilia A

SW Pipe, RR Montgomery, KP Pratt… - Blood, The Journal …, 2016 - ashpublications.org
A normal hemostatic response to vascular injury requires both factor VIII (FVIII) and von
Willebrand factor (VWF). In plasma, VWF and FVIII normally circulate as a noncovalent …

Anti-drug antibodies: emerging approaches to predict, reduce or reverse biotherapeutic immunogenicity

KP Pratt - Antibodies, 2018 - mdpi.com
The development of anti-drug antibodies (ADAs) following administration of biotherapeutics
to patients is a vexing problem that is attracting increasing attention from pharmaceutical …

Engineered antigen-specific human regulatory T cells: immunosuppression of FVIII-specific T-and B-cell responses

YC Kim, AH Zhang, Y Su, SA Rieder… - Blood, The Journal …, 2015 - ashpublications.org
Expansion of human regulatory T cells (Tregs) for clinical applications offers great promise
for the treatment of undesirable immune responses in autoimmunity, transplantation, allergy …

Review of immune tolerance induction in hemophilia A

SJ Schep, REG Schutgens, K Fischer, ML Boes - Blood Reviews, 2018 - Elsevier
At first sight the bleeding disorder hemophilia A seems to have little in common with immune
disorders, but immunology research intersects with other disciplines including hematology …

Tolerating factor VIII: recent progress

S Lacroix-Desmazes, J Voorberg, D Lillicrap… - Frontiers in …, 2020 - frontiersin.org
Development of neutralizing antibodies against biotherapeutic agents administered to
prevent or treat various clinical conditions is a longstanding and growing problem faced by …

[HTML][HTML] Induction of tolerance to factor VIII by transient co‐administration with rapamycin

B Moghimi, BK Sack, S Nayak, DM Markusic… - Journal of Thrombosis …, 2011 - Elsevier
See also Miao CH. Tilt balance towards regulation: evolving new strategy for treatment of
hemophilia inhibitors. This issue, pp 1521–3. DOI: 10.1111/j. 1538‐7836.2011. 04351. x …

HLA-DR-presented peptide repertoires derived from human monocyte-derived dendritic cells pulsed with blood coagulation factor VIII

SD van Haren, E Herczenik, A ten Brinke… - Molecular & Cellular …, 2011 - ASBMB
Activation of T-helper cells is dependent upon the appropriate presentation of antigen-
derived peptides on MHC class II molecules expressed on antigen presenting cells. In the …

CD4+ T-cell epitopes associated with antibody responses after intravenously and subcutaneously applied human FVIII in humanized hemophilic E17 HLA-DRB1 …

KN Steinitz, PM van Helden, B Binder… - Blood, the Journal of …, 2012 - ashpublications.org
Today it is generally accepted that B cells require cognate interactions with CD4+ T cells to
develop high-affinity antibodies against proteins. CD4+ T cells recognize peptides …

Race, ethnicity, F8 variants, and inhibitor risk: analysis of the “My Life Our Future” hemophilia A database

AE Ahmed, KP Pratt - Journal of Thrombosis and Haemostasis, 2023 - Elsevier
Background Several studies have suggested Black and Hispanic hemophilia A (HA) patients
in the United States suffer higher incidences of neutralizing anti-FVIII antibodies (inhibitors) …

Biological considerations of plasma-derived and recombinant factor VIII immunogenicity

J Lai, C Hough, J Tarrant… - Blood, The Journal of the …, 2017 - ashpublications.org
In hemophilia A, the most severe complication of factor VIII (FVIII) replacement therapy
involves the formation of FVIII neutralizing antibodies, also known as inhibitors, in 25% to …