| Literature DB >> 32341561 |
Paul W Barone1, Michael E Wiebe1, James C Leung1, Islam T M Hussein1, Flora J Keumurian1, James Bouressa2,3, Audrey Brussel4,5, Dayue Chen6,7, Ming Chong8, Houman Dehghani9,10, Lionel Gerentes11, James Gilbert12,13, Dan Gold14, Robert Kiss7,15, Thomas R Kreil16, René Labatut4, Yuling Li17,18, Jürgen Müllberg19, Laurent Mallet11,20, Christian Menzel21, Mark Moody22,23, Serge Monpoeho24, Marie Murphy6, Mark Plavsic25,26, Nathan J Roth27, David Roush28, Michael Ruffing29, Richard Schicho30,31, Richard Snyder32, Daniel Stark33, Chun Zhang34,35, Jacqueline Wolfrum1, Anthony J Sinskey1, Stacy L Springs36.
Abstract
Recombinant protein therapeutics, vaccines, and plasma products have a long record of safety. However, the use of cell culture to produce recombinant proteins is still susceptible to contamination with viruses. These contaminations cost millions of dollars to recover from, can lead to patients not receiving therapies, and are very rare, which makes learning from past events difficult. A consortium of biotech companies, together with the Massachusetts Institute of Technology, has convened to collect data on these events. This industry-wide study provides insights into the most common viral contaminants, the source of those contaminants, the cell lines affected, corrective actions, as well as the impact of such events. These results have implications for the safe and effective production of not just current products, but also emerging cell and gene therapies which have shown much therapeutic promise.Entities:
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Year: 2020 PMID: 32341561 DOI: 10.1038/s41587-020-0507-2
Source DB: PubMed Journal: Nat Biotechnol ISSN: 1087-0156 Impact factor: 54.908