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Recombinant Antibody Expression

Beginning this type of work in 1980 while at the NIH, Dr. Cori Gorman has developed methods which allowed for high efficiency gene transfer into a wide variety of cell types including human cells. DNA Bridges®, Inc. can help you with your systems as well.

Gene Expressed Increase in Productivity Status of Project
Chimeric and Humanized Antibodies

Gorman C. (1990) Mammalian cell  expression. Current Opinion. 1:36-47.
 

Redesigned the prototype expression vector which led to up to 1,000-fold increased yield of recombinant protein. Developed a transient expression system which allowed for production of protein at a 1000 fold increase. Milligram quantities produced in a week. U.S. Patent US05024939 issued.
 
Anti-CD11a Humanized Monoclonal and Anti-CD18 Humanized Monoclonal Developed a CHO cell line expression system which allowed for the creation of production lines in 3 months. Genentech is co-developing the anti-CD11a antibody with XOMA Corporation. As of 8/01, Xanelim was in Phase III testing. Genentech investigated the anti-CD18 humanized antibody for the potential treatment acute myocardial infarction. Clinical results did not meet goals and further development was stopped.
 
Anti-HER2 Humanized Monoclonal Antibody Developed a system to allow for rapid production of humanized antibodies. This process cut the time it took to develop a production cell line from 9 months to 3 months.  Genentech has commercialized Herceptin®, the anti-HER2 antibody, as a treatment for breast cancer and continues to evaluate it for other indications.
Anti-IgE Humanized Monoclonal Antibody Developed a system to allow for rapid production of variants of humanized antibodies for in vivo efficacy testing. The small scale transient process developed allowed production of sufficient protein (milligram quantities) in a week rather than 3 months.  Genentech is investigating whether the anti-IgE humanized monoclonal antibody can interfere early in the complex, multistep process that lead to the symptoms of allergy, in patients  who have asthma. Xolair was awaiting FDA approval 8/01.


 

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