maximum allowed levels of these contaminants in the final product. Host cell DNA
might be very sticky and some viruses might attach to either host cell debris or host
cell DNA complicating clarification steps (depth filtration, centrifugation) after
virus harvesting. Salt concentrations/osmolality of media as well as choice of
membrane material and cut-off of the respective filters will need to be screened
thoroughly as each medium and cell line will give a different background and
change of harvest time point will immediately change the cell broth composition.
In order to determine the optimal harvest time point, the ratio of total virus titer to
contaminants should be considered. For attenuated vaccines and viral vectors, a high
infectious titer is necessary to achieve high potency, hence, an early harvest time point
should be targeted. Certain viruses show a low stability, which is characterized by a
steep decrease in infectivity over time. One possible countermeasure is a multiple
harvest strategy, in which the virus is harvested and stored at lower temperature and
new medium is added to the bioreactor. This strategy is often used for adherent cells
and slowly propagating lytic viruses. Moreover, continuous harvesting with sub-
sequent cooling to prevent degradation could also be applied (see chapter 6).
Specific aspects of the intracellular virus replication cycle on process perfor-
mance can also not be neglected. Some viruses bud from the (apical) cell membrane
during virus release and, hence, carry a lipid bilayer as an envelope (see Table 5.9).
Such enveloped viruses are often less stable at higher temperature, sensitive to
lower pH values and fast degraded by contact with detergents; all resulting in in-
fectivity losses. For a few viruses (e.g., MVA), a considerable number of virus
particles remain within the cell. For reaching maximum virus yields, freeze-thaw
cycles or the use of high-pressure homogenizers is recommended to disrupt the cell
membrane and to release the virions.
Another factor to consider during viral vaccine production is the effect of shear
stress (e.g., agitation, pumping) and aeration (e.g., O2 and CO2). High shear forces
can hinder virus binding to the cells or can lead to early cell death and with that to
lower virus titers. Cells go either into apoptosis due to virus infection or into ne-
crosis due to shear stress. For some viruses, such as IAV, the right timing of
apoptosis induction is important for virus release and with that virus yield. It is thus
not as simple as just trying to avoid cell death for as long as possible, to keep cells
productive. It will always be a combination of parameters and events that will result
in higher virus yields. In principle, apoptosis is hallmarked by DNA fragmentation,
plasma-membrane blebbing, and creation of apoptotic bodies (fragmentation) [85].
Different methods (e.g., imaging flow cytometry, NMR spectroscopy, proteomic
approaches) are now established to further investigate cellular bottlenecks during
viral vaccine production that might result in low virus yields (see also chapter 8).
This understanding might help to identify high-producer cells and to optimize
production processes.
Finally, the vaccine type (live-attenuated, inactivated, vector) also has a sig-
nificant impact on design and optimization of virus production processes. Many
attenuated vaccine strains show a lower replication rate and, thus, often reduced
virus yields. In contrast, manufacturing processes for inactivated vaccines that
comprise infectious and non-infectious virus particles often display very high titers.
For production of pathogenic viruses without an option to vaccinate employees
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Bioprocessing of Viral Vaccines