In Vitro Carboxylation of a Blood Coagulation Factor IX Precursor Produced by Recombinant-DNA Technology

1989 ◽  
Vol 61 (02) ◽  
pp. 238-242 ◽  
Author(s):  
Berry A M Soute ◽  
Alain Balland ◽  
Thérèse Faure ◽  
Henri de la Salle ◽  
Cees Vermeer

SummaryBlood coagulation factor IX (Christmas factor) is a plasma protein which is required for normal haemostasis. A functional deficiency of factor IX results in haemophilia B, a bleeding disorder which is generally treated by infusions of factor IX concentrates prepared from pooled human plasma. The use of human blood products is connected with the risk of transmitting viral agents responsible for diseases such as hepatitis B and AIDS. Recombinant DNA techniques may provide the means to produce the required proteins without exposing the patients to these risks and at lower costs. One of the problems which has to be overcome before recombinant factor IX can be used for therapeutical purposes is related to the vitamin K-dependent carboxylation of its 12 NH2-terminal glutamate residues. In cell cultures this carboxylation, which is required to render the protein its procoagulant activity, is far from complete, especially at high expression levels. In this paper we describe the in vitro carboxylation of non and/or partly carboxylated recombinant factor IX produced by transformed Chinese hamster ovary cells. The identity of the newly formed Gla residues was verified and it could be demonstrated that all carboxyl groups had been incorporated into the recombinant factor IX.

2009 ◽  
Vol 11 (10) ◽  
pp. 941-950 ◽  
Author(s):  
Aliakbar Haddad-Mashadrizeh ◽  
Alireza Zomorodipour ◽  
Mehrnaz Izadpanah ◽  
Mohammad Reza Sam ◽  
Fariba Ataei ◽  
...  

2020 ◽  
Vol 20 (1) ◽  
pp. 30-41
Author(s):  
Zh. I. Avdeeva ◽  
A. A. Soldatov ◽  
V. P. Bondarev ◽  
V. A. Merkulov

Hemophilia is an orphan disease associated with deficiency or complete lack of certain blood coagulation factors due to mutation of genes encoding their synthesis. Patients with hemophilia need continuous replacement therapy with coagulation factor products which are produced by recombinant DNA technology or derived from donated blood plasma. The development of new products or improvement of the production process of already authorised medicinal products involve clinical trials that have to include both previously treated and untreated patients of different age groups. The aim of the paper was to perform an analytical review of general hemophilia issues and major requirements for clinical trials of coagulation factor IX products based on the updated documents of the European Medicines Agency. The paper summarises the basic principles of conducting clinical trials of coagulation factor IX products that are submitted for marketing authorisation as “new” products, based on recommendations of Russian and international regulatory documents, including the updated guideline of the European Medicines Agency. It sums up product safety issues associated with undesirable immunogenicity resulting in formation of inhibitors that provoke allergic reactions or reduce the effectiveness of therapy. The harmonisation of the requirements for clinical trials during preparation and updating of documents by Russian manufacturers should be based on the analysis of the experience with hemophilia products and latest scientific achievements in the disease treatment. In that case it will facilitate the introduction of innovative efficacious hemophilia products into clinical practice.


1988 ◽  
Vol 7 (5) ◽  
pp. 613-632
Author(s):  
John M. Beals ◽  
Joseph Weber ◽  
Paul Derwent ◽  
Kenneth L. Grant ◽  
Francis J. Castellino

2015 ◽  
Vol 39 (10) ◽  
pp. 1162-1172 ◽  
Author(s):  
Hisataka Kitano ◽  
Atsushi Mamiya ◽  
Ishikawa Tomomi ◽  
Kokubun Shinichiro ◽  
Hidai Chiaki

Peptides ◽  
1992 ◽  
pp. 241-242
Author(s):  
Linda H. Huang ◽  
Hong Cheng ◽  
Arthur Pardi ◽  
James P. Tam ◽  
William V. Sweeney

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