Emerging roles of protein mannosylation in inflammation and infection
Proteins are frequently modified by complex carbohydrates (glycans) that play central roles
in maintaining the structural and functional integrity of cells and tissues in humans and lower …
in maintaining the structural and functional integrity of cells and tissues in humans and lower …
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 …
prevent or treat various clinical conditions is a longstanding and growing problem faced by …
Advances in knowledge of inhibitor formation in severe haemophilia A
M Cormier, P Batty, J Tarrant… - British Journal of …, 2020 - Wiley Online Library
Anti‐drug antibody formation following factor VIII (FVIII) replacement therapy is the most
important treatment‐related complication in patients with severe haemophilia A. A significant …
important treatment‐related complication in patients with severe haemophilia A. A significant …
Tolerogenic dendritic cells generated in vitro using a novel protocol mimicking mucosal tolerance mechanisms represent a potential therapeutic cell platform for …
G Dao Nyesiga, L Pool, PC Englezou… - Frontiers in …, 2023 - frontiersin.org
Dendritic cells (DCs) are mediators between innate and adaptive immunity and vital in
initiating and modulating antigen-specific immune responses. The most important site for …
initiating and modulating antigen-specific immune responses. The most important site for …
Race, ethnicity, F8 variants, and inhibitor risk: analysis of the “My Life Our Future” hemophilia A database
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) …
in the United States suffer higher incidences of neutralizing anti-FVIII antibodies (inhibitors) …
Induction of activated T follicular helper cells is critical for anti-FVIII inhibitor development in hemophilia A mice
W Jing, J Chen, Y Cai, Y Chen, JA Schroeder… - Blood …, 2019 - ashpublications.org
The development of neutralizing anti-FVIII antibodies (inhibitors) is a major complication of
FVIII protein replacement therapy in patients with hemophilia A (HA). Although multiple lines …
FVIII protein replacement therapy in patients with hemophilia A (HA). Although multiple lines …
MAPPs for the identification of immunogenic hotspots of biotherapeutics; an overview of the technology and its application to the biopharmaceutical arena
V Quarmby, QT Phung, JR Lill - Expert Review of Proteomics, 2018 - Taylor & Francis
Introduction: Anti-drug antibody (ADA) responses are becoming an increasing concern as
more highly engineered and sophisticated biotherapeutics enter the clinic. An arsenal of …
more highly engineered and sophisticated biotherapeutics enter the clinic. An arsenal of …
An observational study from long-term AAV re-administration in two hemophilia dogs
J Sun, W Shao, X Chen, EP Merricks, L Wimsey… - … Therapy Methods & …, 2018 - cell.com
Adeno-associated virus (AAV) vectors have been successfully applied in hemophilia clinical
trials. However, this approach is limited to patients without AAV-neutralizing antibodies …
trials. However, this approach is limited to patients without AAV-neutralizing antibodies …
Discoidin domains as emerging therapeutic targets
BO Villoutreix, MA Miteva - Trends in pharmacological sciences, 2016 - cell.com
Discoidin (DS) domains are found in eukaryotic and prokaryotic extracellular and
transmembrane multidomain proteins. These small domains play different functional roles …
transmembrane multidomain proteins. These small domains play different functional roles …
To serve and protect: the modulatory role of von Willebrand factor on factor VIII immunogenicity
RB Hartholt, AS van Velzen, I Peyron, A Ten Brinke… - Blood reviews, 2017 - Elsevier
Hemophilia A is a bleeding disorder characterized by the absence or dysfunction of blood
coagulation factor VIII (FVIII). Patients are treated with regular infusions of FVIII concentrate …
coagulation factor VIII (FVIII). Patients are treated with regular infusions of FVIII concentrate …