Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
6003262 | Thrombosis Research | 2013 | 11 Pages |
Abstract
Human-cl rhFVIII is confirmed to be sulfated and glycosylated comparable to human plasma-derived FVIII. Most importantly, human-cl rhFVIII is devoid of the antigenic Neu5Gc or α-Gal epitopes observed in Chinese Hamster Ovary- and Baby Hamster Kidney-derived rFVIII products. Both the avoidance of non-human glycan structures and the achievement of complete sulfation are proposed to lower the intrinsic immunogenicity of human-cl rhFVIII compared with current rFVIII products.
Keywords
PTMFactor VIII inhibitorsKdnBHKFVIIIITITOFHPAEC-PADNeu5AcvWFNeu5Gcα-galHEKMS/MSAsparagineN-acetylneuraminic acidN-glycolylneuraminic acidimmune tolerance inductionChobaby hamster kidneyTandem MSChinese Hamster Ovarypost-translational modificationsTyrosinetime of flightMass spectrometryVon Willebrand factorFactor VIIIEICHaemophilia Aliquid chromatographyhigh performance anion exchange chromatography with pulsed amperometric detectionextracted ion chromatogramhuman embryonic kidney
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Authors
Christoph Kannicht, Margareta Ramström, Guido Kohla, Maya Tiemeyer, Elisabeth Casademunt, Olaf Walter, Helena Sandberg,