TY - JOUR
T1 - An update on the ‘danger theory’ in inhibitor development in hemophilia A
AU - Schep, Sarah J
AU - Boes, Marianne L
AU - Schutgens, Roger E G
AU - van Vulpen, Lize F D
N1 - Funding Information:
Contrary to the well-established relationship between FVIII mutation and inhibitor risk, this association is less clear for environmental factors, including the FVIII product type as potential risk factor. Until recently, studies regarding this issue showed contradictory and/or inconclusive results [34–36]. The SIPPET study was specifically designed to answer this question. It is the first and only randomized controlled trial showing an increased inhibitor risk by recombinant FVIII (rFVIII) products compared to plasma-derived FVIII (pd-FVIII) [37]. This is supported by a French national cohort study [24]. Proposed explanations for this finding include the presence of Von Willebrand Factor (VWF) in pd-FVIII, reducing FVIII immunogenicity by epitope masking and prevention of endocytosis by DCs. Secondly, the different posttranslational modifications of rFVIII due to its production in mammalian cells rather than human cells might influence its immunogenicity [38–42]. This issue however remains highly debated, which is beyond the scope of this review.
Publisher Copyright:
© 2019, © 2019 Informa UK Limited, trading as Taylor & Francis Group.
PY - 2019/5
Y1 - 2019/5
N2 - Introduction: Nowadays, one of the most serious treatment complications in hemophilia A is the formation of neutralizing antibodies against coagulation factor VIII (FVIII). These so-called inhibitors develop in about 30% of all patients with severe hemophilia A. Once formed, inhibitors reduce FVIII efficacy in blood coagulation, which has a negative impact on patients’ health and quality of life and significantly increases hemophilia A treatment costs. The pathophysiology of inhibitor development is a complex and multi-causal process, in which both genetic factors as well as environmental factors participate. So-called ‘danger signals’ are considered contributors to inhibitor formation, and can be triggered by surgery, joint bleeds or infections. A pro-inflammatory tissue micro-environment is thereby established, which is characterized by the upregulation of costimulatory molecules on antigen-presenting cells (APCs), that can facilitate the alloimmunization to FVIII and thereby inhibitor formation. Here, the authors will discuss evidence from (pre)clinical studies about this theory in hemophilia A. Areas covered: In this review, the current knowledge regarding the ‘danger theory’ with regard to inhibitor development in hemophilia A is summarized. Expert opinion: Danger signals might contribute to inhibitor development; however, the evidence is scarce and not conclusive. Future studies, like multinational registries, are warranted but challenging.
AB - Introduction: Nowadays, one of the most serious treatment complications in hemophilia A is the formation of neutralizing antibodies against coagulation factor VIII (FVIII). These so-called inhibitors develop in about 30% of all patients with severe hemophilia A. Once formed, inhibitors reduce FVIII efficacy in blood coagulation, which has a negative impact on patients’ health and quality of life and significantly increases hemophilia A treatment costs. The pathophysiology of inhibitor development is a complex and multi-causal process, in which both genetic factors as well as environmental factors participate. So-called ‘danger signals’ are considered contributors to inhibitor formation, and can be triggered by surgery, joint bleeds or infections. A pro-inflammatory tissue micro-environment is thereby established, which is characterized by the upregulation of costimulatory molecules on antigen-presenting cells (APCs), that can facilitate the alloimmunization to FVIII and thereby inhibitor formation. Here, the authors will discuss evidence from (pre)clinical studies about this theory in hemophilia A. Areas covered: In this review, the current knowledge regarding the ‘danger theory’ with regard to inhibitor development in hemophilia A is summarized. Expert opinion: Danger signals might contribute to inhibitor development; however, the evidence is scarce and not conclusive. Future studies, like multinational registries, are warranted but challenging.
KW - haemophilia
KW - danger signals
KW - Inhibitors
KW - intensive treatment
KW - risk factors
KW - inhibitors
KW - Haemophilia
UR - http://www.scopus.com/inward/record.url?scp=85065193479&partnerID=8YFLogxK
U2 - 10.1080/17474086.2019.1604213
DO - 10.1080/17474086.2019.1604213
M3 - Review article
C2 - 30951401
SN - 1747-4086
VL - 12
SP - 335
EP - 344
JO - Expert Review of Hematology
JF - Expert Review of Hematology
IS - 5
ER -