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haematologica | 2021; 106(3)
ERRATA CORRIGE
Dissecting the pathophysiology of immune thrombotic thrombocytopenic purpura: interplay between genes and environmental triggers
Johana Hrdinová,1,2,3* Silvia D’Angelo,4,5* Nuno A. G. Graça,1,6* Bogac Ercig,1,2,3 Karen Vanhoorelbeke,4 Agnès Veyradier,7,8 Jan Voorberg1 and Paul Coppo8,9,10
1Department of Plasma Proteins, Sanquin-Academic Medical Center Landsteiner Laboratory, Amsterdam, the Netherlands; 2PharmaTarget B.V., Maastricht, the Netherlands; 3Department of Biochemistry, Cardiovascular Research Institute Maastricht (CARIM), Maastricht University, the Netherlands; 4Laboratory for Thrombosis Research, IRF Life Sciences, KU Leuven Campus Kulak Kortrijk, Belgium; 5Protobios LLC, Tallinn, Estonia; 6Icosagen Cell Factory OÜ, Ülenurme Vald, Tartumaa, Estonia; 7Service d'Hématologie Biologique and EA3518, Groupe Hospitalier Saint Louis-Lariboisière, Assistance Publique - Hôpitaux de Paris, Université Paris Diderot, France; 8Centre de Référence des Microangiopathies Thrombotiques, Hôpital Saint-Antoine, AP-HP, Paris, France; 9Service d’Hématologie, Assistance Publique – Hôpitaux de Paris, France and 10Sorbonne Université, UPMC Univ Paris 06, France
Published in Haematologica 2018;103(7):1099-1109.
*JH, SD’A and NAGG contributed equally as co-first authors.
doi:10.3324/haematol.2020.278244
On page 1100-1101 we would like to change the sentence:
©2021 Ferrata Storti Foundation
“The clinical significance of the restricted VH1-69 germline gene segment has been observed in neutralizing Abs directed toward a highly conserved region in the hemagglutinin ectodomain of the influenza virus35 and in patients with B-cell lymphoma after chronic hepatitis C infection.36”
to:
“Antibodies directed towards the ectodomain of hemagglutinin of the influenza virus as well as hepatitis C virus are also frequently encoded by VH1-69 germline gene segments.35,36”
On page 1103 we would like to change the sentence:
“Activation of ADAMTS13-specific CD4+ T cells requires uptake of ADAMTS13 by antigen-presenting cells (APCs) and presentation of ADAMTS13-derived peptides on HLA molecules. As the HLA-DRB1*11 was identified as a risk fac- tor for the development of iTTP, investigation of ADAMTS13-derived peptides that are preferentially presented on MHC class II of healthy individuals positive for this allele was performed.66”
to:
“Proteolytic degradation of endocytosed ADAMTS13 in endo-lysosomal compartments in antigen-presenting cells has been shown to result in presentation of ADAMTS13-derived peptides on MHC class II molecules. It has been well- established that HLA-DRB1*11 is a risk factor for the development of iTTP.57,58 This prompted us to explore the reper- toire of ADAMTS13-derived peptides presented on this risk allele for iTTP.66 “
On page 1105 we would like to change the sentence:
“Raised VWF levels are required to induce TTP in Adamts13-/- mice, but varying the concentration between 20 and 120 U/mL does not appear to affect the occurrence or severity of the disease, suggesting that a threshold level of VWF is sufficient, and that higher levels confer little additional risk. However, humans appear to be more sensitive to changes in VWF levels than mice. Women with inherited ADAMTS13 deficiency frequently develop TTP during pregnancy, which probably results from the progressive increase in VWF levels throughout the gestation period. Moreover, obese individuals have higher levels of VWF, providing further evidence for an association between obesity and TTP. Thus, changes in VWF secretion, multimer distribution, and plasma level may trigger TTP.78”
to:
“A threshold level of VWF has been suggested to promote shiga toxin-induced TTP in Adamts13−/− mice.78 During preg- nancy VWF levels increase progressively; this may contribute to the development of microvascular thrombosis in preg- nant woman with congenital or immune-mediated TTP.78 Moreover, obese individuals have higher levels of VWF, pro- viding further evidence for an association between obesity and TTP. These findings raise the possibility that elevated levels of VWF may contribute to the onset of TTP in various physiological or clinical conditions.78”