Pregled bibliografske jedinice broj: 989784
Degradation Products of Factor VIII Which Can Lead to Increased Immunogenicity
Degradation Products of Factor VIII Which Can Lead to Increased Immunogenicity // Vox Sanguinis, 77 (1999), Suppl. 1; 90-99 doi:10.1159/000056726 (međunarodna recenzija, članak, stručni)
CROSBI ID: 989784 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Degradation Products of Factor VIII Which Can Lead to Increased Immunogenicity
Autori
Josic´ ; , Djuro ; Buchacher, Andrea ; Kannicht, Christoph ; Lim, Yow-Pin ; Lö ; ster, Klemens ; Pock, Katharina ; Robinson, Stephen ; Schwinn, Horst ; Stadler, Monika
Izvornik
Vox Sanguinis (0042-9007) 77
(1999), Suppl. 1;
90-99
Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, stručni
Ključne riječi
Factor VIII ; Immunogenicity
Sažetak
The biochemical and immunochemical aspects of the development of inhibitors with a plasma-derived, double-virus inactivated factor VIII (FVIII) concentrate (marketed as Octavi SDPlus in Germany and Bisinact in Belgium) are described. A total of 12 cases of inhibitor formation (predominantly type II) were reported in Germany, 8 in Belgium but none in Portugal. Initially, the only difference between the non-pasteurised, SD virus-inactivated product Octavi and the pasteurised product Octavi SDPlus appeared to be pasteurisation, though subsequently, the quality of source material for the product was found to differ in different countries. Separation studies revealed the presence of a 40 kDa peptide fragment in some batches. It was subsequently shown that there was a strong correlation between inhibitor development and batches containing the 40 kDa marker, and a relationship between elevated markers of coagulation activation (FPA in particular) and the occurrence of the 40 kDa marker. Further work revealed that analytical methods commonly used for quality control were not suitable to highlight batch-to-batch differences. It was concluded that inhibitor potential (neoantigenicity) in Octavi SDPlus arose due to two effects ; degradation of FVIII already present in source material ; and heating of unstable FVIII degradation products. In this case, inhibitors were not caused by the overall production process, nor by GMP failures. The problem of inhibitor potential can be avoided if appropriate preventive measures are taken. Further work is needed to prove non-neoantigenicity and to reinforce the scientific findings, and to characterise pilot batches.
Izvorni jezik
Engleski
Znanstvena područja
Biotehnologija u biomedicini (prirodno područje, biomedicina i zdravstvo, biotehničko područje)
POVEZANOST RADA
Ustanove:
Sveučilište u Rijeci - Odjel za biotehnologiju
Citiraj ovu publikaciju:
Časopis indeksira:
- Current Contents Connect (CCC)
- Web of Science Core Collection (WoSCC)
- Science Citation Index Expanded (SCI-EXP)
- SCI-EXP, SSCI i/ili A&HCI
- Scopus
- MEDLINE